Unravelling the synthetic and therapeutic aspects of five, six and fused heterocycles using Vilsmeier-Haack reagent

The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier-Haack (V. H.) reagent. These derivatives act as excellent precursors having different aryl ring functionalities and could be used for the synthesis of...

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Published in:RSC advances Vol. 13; no. 38; pp. 2664 - 26629
Main Authors: Chahal, Mamta, Dhillon, Sudeep, Rani, Priyanka, Kumari, Ginna, Aneja, Deepak Kumar, Kinger, Mayank
Format: Journal Article
Language:English
Published: Cambridge Royal Society of Chemistry 05.09.2023
The Royal Society of Chemistry
Subjects:
Anticonvulsants
Chemical synthesis
Chemistry
Heterocyclic compounds
Organic chemistry
Precursors
Reagents
ISSN:2046-2069, 2046-2069
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Abstract The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier-Haack (V. H.) reagent. These derivatives act as excellent precursors having different aryl ring functionalities and could be used for the synthesis of a variety of heterocyclic scaffolds. The V. H. reagent, a versatile reagent in organic chemistry, is used to formylate various heterocyclic compounds of medicinal interest. Due to the different chemical interactions, efficacy, and potency of V. H. reagents, plenty of heterocyclic compounds can be synthesized which serve as a constituent in various novel medications and acts as a bridge between biology and chemistry. These carboxylate moieties can effectively cooperate as precursors for several multi-component reactions (MCR) including Strecker synthesis, Bucherer-Berg reaction and post-MCR cyclization, modified variants with various pharmaceutical applications such as anti-tumor, anti-convulsant, anti-chitosomal and so on. The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier-Haack (V. H.) reagent.
AbstractList The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier-Haack (V. H.) reagent. These derivatives act as excellent precursors having different aryl ring functionalities and could be used for the synthesis of a variety of heterocyclic scaffolds. The V. H. reagent, a versatile reagent in organic chemistry, is used to formylate various heterocyclic compounds of medicinal interest. Due to the different chemical interactions, efficacy, and potency of V. H. reagents, plenty of heterocyclic compounds can be synthesized which serve as a constituent in various novel medications and acts as a bridge between biology and chemistry. These carboxylate moieties can effectively cooperate as precursors for several multi-component reactions (MCR) including Strecker synthesis, Bucherer-Berg reaction and post-MCR cyclization, modified variants with various pharmaceutical applications such as anti-tumor, anti-convulsant, anti-chitosomal and so on. The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier-Haack (V. H.) reagent.
The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier–Haack (V. H.) reagent. These derivatives act as excellent precursors having different aryl ring functionalities and could be used for the synthesis of a variety of heterocyclic scaffolds. The V. H. reagent, a versatile reagent in organic chemistry, is used to formylate various heterocyclic compounds of medicinal interest. Due to the different chemical interactions, efficacy, and potency of V. H. reagents, plenty of heterocyclic compounds can be synthesized which serve as a constituent in various novel medications and acts as a bridge between biology and chemistry. These carboxylate moieties can effectively cooperate as precursors for several multi-component reactions (MCR) including Strecker synthesis, Bucherer–Berg reaction and post-MCR cyclization, modified variants with various pharmaceutical applications such as anti-tumor, anti-convulsant, anti-chitosomal and so on.
The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier–Haack (V. H.) reagent. These derivatives act as excellent precursors having different aryl ring functionalities and could be used for the synthesis of a variety of heterocyclic scaffolds. The V. H. reagent, a versatile reagent in organic chemistry, is used to formylate various heterocyclic compounds of medicinal interest. Due to the different chemical interactions, efficacy, and potency of V. H. reagents, plenty of heterocyclic compounds can be synthesized which serve as a constituent in various novel medications and acts as a bridge between biology and chemistry. These carboxylate moieties can effectively cooperate as precursors for several multi-component reactions (MCR) including Strecker synthesis, Bucherer–Berg reaction and post-MCR cyclization, modified variants with various pharmaceutical applications such as anti-tumor, anti-convulsant, anti-chitosomal and so on. The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier–Haack (V. H.) reagent.
The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier-Haack (V. H.) reagent. These derivatives act as excellent precursors having different aryl ring functionalities and could be used for the synthesis of a variety of heterocyclic scaffolds. The V. H. reagent, a versatile reagent in organic chemistry, is used to formylate various heterocyclic compounds of medicinal interest. Due to the different chemical interactions, efficacy, and potency of V. H. reagents, plenty of heterocyclic compounds can be synthesized which serve as a constituent in various novel medications and acts as a bridge between biology and chemistry. These carboxylate moieties can effectively cooperate as precursors for several multi-component reactions (MCR) including Strecker synthesis, Bucherer-Berg reaction and post-MCR cyclization, modified variants with various pharmaceutical applications such as anti-tumor, anti-convulsant, anti-chitosomal and so on.The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier-Haack (V. H.) reagent. These derivatives act as excellent precursors having different aryl ring functionalities and could be used for the synthesis of a variety of heterocyclic scaffolds. The V. H. reagent, a versatile reagent in organic chemistry, is used to formylate various heterocyclic compounds of medicinal interest. Due to the different chemical interactions, efficacy, and potency of V. H. reagents, plenty of heterocyclic compounds can be synthesized which serve as a constituent in various novel medications and acts as a bridge between biology and chemistry. These carboxylate moieties can effectively cooperate as precursors for several multi-component reactions (MCR) including Strecker synthesis, Bucherer-Berg reaction and post-MCR cyclization, modified variants with various pharmaceutical applications such as anti-tumor, anti-convulsant, anti-chitosomal and so on.
Author Kinger, Mayank
Chahal, Mamta
Rani, Priyanka
Kumari, Ginna
Aneja, Deepak Kumar
Dhillon, Sudeep
AuthorAffiliation Department of Chemistry
Chaudhary Bansi Lal University
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Cites_doi 10.1007/s10593-015-1789-z
10.1016/j.ejmech.2015.05.037
10.1248/cpb.51.838
10.1039/C6RA06093E
10.1007/s10534-011-9496-4
10.1002/ps.7349
10.2166/wst.2016.414
10.3998/ark.5550190.0007.b07
10.1055/s-0035-1561459
10.1080/00304948.2017.1342511
10.1002/ejoc.201800249
10.1002/jhet.3894
10.1134/S1070363218060099
10.1021/jm070528f
10.1038/nrd1034
10.1016/j.matpr.2018.06.560
10.1016/j.ejmech.2014.09.001
10.1016/j.bmc.2007.12.033
10.1080/00397910500290573
10.1016/j.molstruc.2018.11.030
10.1016/j.tet.2011.06.040
10.1007/s10965-021-02672-1
10.21833/ijaas.2021.06.015
10.1016/j.jsps.2012.03.002
10.1016/j.ejmech.2016.05.043
10.1016/j.jscs.2014.12.004
10.1246/cl.150133
10.1016/j.cdc.2022.100930
10.1007/s11164-016-2738-x
10.3390/M1136
10.1016/j.ejmech.2007.12.006
10.1002/bkcs.11673
10.3390/antibiotics9100650
10.1021/jo801492k
10.1021/jf100872f
10.1080/00397911.2014.994128
10.9734/ACSJ/2012/1063
10.1002/jhet.5570390503
10.1134/S1070363219060161
10.2174/138955707781662645
10.1016/j.tet.2008.03.038
10.1016/j.ejmech.2014.11.042
10.1016/j.ejmech.2016.12.059
10.1021/jm010032c
10.2298/JSC0607713C
10.1039/C0OB00771D
10.1002/cber.19270600118
10.1016/j.ejmech.2006.12.032
10.1002/1521-4184(200205)335:5<213::AID-ARDP213>3.0.CO;2-H
10.1134/S1070428019100087
10.1016/j.tetlet.2016.02.045
10.1016/j.tetlet.2010.03.117
10.1016/S0091-3057(84)80027-1
10.1002/jhet.338
10.3390/molecules26102907
10.4314/tjpr.v15i12.12
10.1016/j.bmcl.2015.11.038
10.1021/jm070821f
10.1016/B978-0-08-052349-1.00049-4
10.1002/jhet.3824
10.1021/jo101949y
10.1080/00397911.2020.1750033
10.1016/j.tetlet.2021.153297
10.1039/C8OB03040E
10.1002/jhet.3849
10.1016/j.crci.2017.12.001
10.3998/ark.5550190.0007.a17
10.1134/S0036024417020182
10.1002/jhet.1506
10.1134/S1070428017010110
10.3390/molecules25122758
10.1063/5.0093601
10.1248/cpb.52.307
10.1016/j.jksus.2022.102023
10.1155/2021/2408006
10.1016/j.ejmech.2017.04.002
10.1007/s11696-022-02066-7
10.1016/j.ejmech.2006.09.006
10.1007/s00706-020-02733-z
10.1021/jm060499t
10.1016/S0039-6257(99)00079-X
10.1134/S1070363217100280
10.1002/jhet.3282
10.1016/j.ejmech.2014.11.059
10.1055/s-0036-1588992
10.1007/s40843-017-9084-x
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Notes Mamta Chahal was born in Jind district, Haryana state, India. She obtained her Bachelor's degree in 2017 and master's degree in organic chemistry from Kurukshetra university, Kurukshetra in 2019. She is persuing her PhD degree with Dr Mayank Kinger, Associate professor, at Chaudhary Bansi Lal University, Haryana, India. Her research area is the synthetic utility of novel heterocycles.
Sudeep Dhillon was born and grew up in Dahola, Jind, Haryana, India. Sudeep Dhillon obtained his bachelor's degree in Non-medical from Panjab University, Chandigarh in 2015 and his Master's in Organic Chemistry from Maharishi Markandeshwar University, Mullana, India in 2017. He is pursuing his PhD degree from Chaudhary Bansi Lal University, Bhiwani, India with Dr Mayank Kinger, Associate Professor, Chaudhary Bansi Lal University, Bhiwani, India. His current research interests are the synthesis of new biologically potent heterocycles (anti-cancer, anti-Alzheimer, anti-inflammatory
Priyanka Rani was born in Bhiwani district, Haryana, India. She received her BSc degree in 2015 from Maharshi Dayanand University, Rohtak, and her M.Sc degree in 2017 from Baba Mastnath University, Rohtak. Now she is continuing her study at Chaudhary Bansi Lal University with Dr Mayank Kinger, Associate Professor, Chaudhary Bansi Lal University, Bhiwani, India conducting research work. Her current research interest focuses on five or six-membered heterocycles with pharmaceutical potential such as anti-diabetic, anti-anxiety, anti-malarial, anti-inflammatory, anti-fungal activity
Deepak Kumar was born in the small village of Saniana of District Fatehabad of Haryana State and obtained his early education from the village. He obtained his BSc in 2004 from CRM Jat (PG) College, Hisar and his MSc in 2006 from Kurukshetra University, Kurukshetra, India. He then joined Jubilant Chemsys Ltd, Noida, as Research Associate and worked there for 2 years from 2006 to 2008. Then, he moved back to Kurukshetra University and Joined the research group of Professor Om Prakash for his PhD studies. He submitted his PhD thesis in 2012 and defended in 2013. He joined GDC Memorial College, Bahal, Bhiwani in 2012 and worked as Assistant Professor for 3 years. In 2015, he joined Chaudhary Bansi Lal University, Haryana as Assistant Professor and is working on the reactivity of hypervalent iodine reagents under different reaction conditions and their importance in different fields of science.
Mayank Kinger obtained his bachelor's degree in Medical Science from C.C.S. University, Meerut, India in 2000. He obtained his Master's in Organic Chemistry from C.C.S. University, Meerut, India in 2002. He received his PhD degree from Kurukshetra University, Kurukshetra, India in 2008 under the supervision of Prof. Om Prakash, Emeritus Professor, Kurukshetra University. He was a postdoctoral fellow at Korea Atomic Energy Research Institute, South Korea from 2010 to 2012. Then, he joined M.M. University, Mullana, Ambala, India. In 2018, he joined Chaudhary Bansi Lal University, Haryana as Associate Professor. His current research interests are synthesis of new biologically potent heterocycles (anti-cancer, anti-Alzheimer, anti-inflammatory, anti-bacterial, anti-fungal agents
etc.
Ginna Kumari was born and grew up in Charkhi Dadri district, Haryana, India. She obtained her bachelor's degree in 2013 from Maharshi Dayanand University, Rohtak, and her master's degree in chemistry in 2016 from Panjab University, Chandigarh, India. She is currently working with Dr Mayank Kinger, in the Department of Chemistry, Chaudhary Bansilal University, Haryana, India. Her research interest is the synthesis of novel heterocycles.
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References Delancey (D3RA04309F/cit42/1) 2020; 9
El-Mekabaty (D3RA04309F/cit46/1) 2020; 57
Magedov (D3RA04309F/cit21/1) 2007; 50
Kasmi-Mir (D3RA04309F/cit62/1) 2018; 11
Abadi (D3RA04309F/cit16a/1) 2003; 51
Builla (D3RA04309F/cit4/1) 2011; 1
Mathew (D3RA04309F/cit23/1) 2012; 2
Zhang (D3RA04309F/cit32/1) 2017; 127
Farghaly (D3RA04309F/cit25b/1) 2006; 11
Abadi (D3RA04309F/cit20/1) 2003; 51
Irgashev (D3RA04309F/cit107/1) 2021; 79
Bala (D3RA04309F/cit51/1) 2018; 55
Ozdemir (D3RA04309F/cit26/1) 2007; 42
El-Desoky (D3RA04309F/cit11/1) 2017; 2
Swami (D3RA04309F/cit50/1) 2016; 57
Pahutski (D3RA04309F/cit60/1) 2023; 79
Panneer (D3RA04309F/cit33/1) 2011; 1
Duguta (D3RA04309F/cit106/1) 2020; 50
Ziajahromi (D3RA04309F/cit7/1) 2016; 74
Pervaram (D3RA04309F/cit47/1) 2017; 87
Hu (D3RA04309F/cit89/1) 2015; 44
Datoussaid (D3RA04309F/cit71/1) 2020; 1
Gupton (D3RA04309F/cit74/1) 2008; 64
Benaamane (D3RA04309F/cit22b/1) 2008; 16
Abdelwahab (D3RA04309F/cit98/1) 2017; 49
Popov (D3RA04309F/cit58/1) 2019
Dong (D3RA04309F/cit102/1) 2005; 1
Enguehard-Gueiffier (D3RA04309F/cit87/1) 2007; 7
Hung (D3RA04309F/cit96/1) 2014; 86
Tang (D3RA04309F/cit2/1) 2008; 73
Naik (D3RA04309F/cit108/1) 2018; 5
Sathiyaseelan (D3RA04309F/cit52/1) 2016; 4
Tang (D3RA04309F/cit72/1) 2019; 40
Reddy (D3RA04309F/cit8/1) 2004; 52
Nagamallu (D3RA04309F/cit49/1) 2016; 26
Hu (D3RA04309F/cit31/1) 2017; 20
Fadavi (D3RA04309F/cit63/1) 2018; 21
Abdi (D3RA04309F/cit79/1) 2021
Chovatia (D3RA04309F/cit24/1) 2007; 71
Gao (D3RA04309F/cit109/1) 2017; 60
Prakash (D3RA04309F/cit75/1) 2005; 35
Bebernitz (D3RA04309F/cit17/1) 2001; 44
Kumar (D3RA04309F/cit40/1) 2018; M1011
Zhang (D3RA04309F/cit70/1) 2011; 76
Kumari (D3RA04309F/cit39/1) 2020; 57
Hafez (D3RA04309F/cit9/1) 2008; 43
Chung (D3RA04309F/cit100/1) 2021; 26
Flower (D3RA04309F/cit16b/1) 2003; 2
Farat (D3RA04309F/cit105/1) 2021; 152
AppiáReddy (D3RA04309F/cit82/1) 2011; 9
Tingle (D3RA04309F/cit10/1) 2003
Shetty (D3RA04309F/cit54/1) 2020; 30
Szabo (D3RA04309F/cit22a/1) 2008; 51
El-Gharably (D3RA04309F/cit37/1) 2022; 29
Husain (D3RA04309F/cit95/1) 2022; 34
Vilsmeier (D3RA04309F/cit3/1) 1927; 60
Vellalacheruvu (D3RA04309F/cit80/1) 2017; 3
Gilbert (D3RA04309F/cit19/1) 2006; 49
Katz (D3RA04309F/cit15/1) 1984; 21
Ahmad (D3RA04309F/cit6/1) 2016; 20
Keter (D3RA04309F/cit35/1) 2012; 25
Taber (D3RA04309F/cit92/1) 2011; 67
Al-Thakafy (D3RA04309F/cit84/1) 2022; 65
Mamatha (D3RA04309F/cit57/1) 2022; 41
Rajput (D3RA04309F/cit59/1) 2015; 12
Aparna (D3RA04309F/cit61/1) 2019; 89
Aeluri (D3RA04309F/cit85/1) 2015; 100
Koval (D3RA04309F/cit69/1) 2017; 91
Abdelwahab (D3RA04309F/cit97/1) 2016; 48
Chami (D3RA04309F/cit103/1) 2017; 8
Al-Lami (D3RA04309F/cit86/1) 2018; 10
Mohammed (D3RA04309F/cit68/1) 2022; 76
Marella (D3RA04309F/cit77/1) 2013; 21
Derry (D3RA04309F/cit13/1) 2010; 8
Antuf’eva (D3RA04309F/cit88/1) 2018; 88
Saudi (D3RA04309F/cit29/1) 2016; 121
Sener (D3RA04309F/cit27/1) 2002; 39
Saoud (D3RA04309F/cit101/1) 2020; 10
Eftekhari-Sis (D3RA04309F/cit93/1) 2010; 47
Sun (D3RA04309F/cit81/1) 2018
Quiroga (D3RA04309F/cit91/1) 2010; 51
Zaman (D3RA04309F/cit83/1) 2019; 1180
El-Assiery (D3RA04309F/cit90/1) 2004; 54
Mphahlele (D3RA04309F/cit78/1) 2019; 17
Hashem (D3RA04309F/cit25a/1) 2007; 42
Potopnyk (D3RA04309F/cit48/1) 2017; 53
Sangwan (D3RA04309F/cit34/1) 1980; 19
Tadtong (D3RA04309F/cit110/1) 2016; 15
Scriven (D3RA04309F/cit67/1) 2000
Fahmy (D3RA04309F/cit28/1) 2002; 335
Cohn (D3RA04309F/cit1/1) 1991; 2
Pawar (D3RA04309F/cit5/1) 2020
Noh (D3RA04309F/cit104/1) 2020
Marmor (D3RA04309F/cit12/1) 1999; 44
Mishra (D3RA04309F/cit38/1) 2020; 9
Farghaly (D3RA04309F/cit25c/1) 2006
Shelkovnikov (D3RA04309F/cit66/1) 2019; 55
Alnufaie (D3RA04309F/cit44/1) 2020; 25
Nashaan (D3RA04309F/cit56/1) 2023; 7
Faraj (D3RA04309F/cit94/1) 2022; 2398
Raghavendra (D3RA04309F/cit41/1) 2015; 7
Manvar (D3RA04309F/cit30/1) 2015; 90
Bhat (D3RA04309F/cit55/1) 2016; 6
Hon (D3RA04309F/cit43/1) 2020; 57
Padalkar (D3RA04309F/cit45/1) 2016; 53
Barman (D3RA04309F/cit64/1) 2015; 51
Puljak (D3RA04309F/cit14/1) 2017; 5
Chamberlain (D3RA04309F/cit18/1) 2010; 58
Zarei (D3RA04309F/cit73/1) 2017; 49
Abd Allah (D3RA04309F/cit53/1) 2015; 45
Küçükgüzel (D3RA04309F/cit36/1) 2015; 97
Al-Dmour (D3RA04309F/cit65/1) 2021; 8
Gonçalves (D3RA04309F/cit99/1) 2018; 9
Zarei (D3RA04309F/cit76/1) 2017; 43
References_xml – volume: 10
  start-page: 3344
  year: 2018
  ident: D3RA04309F/cit86/1
  publication-title: Sci. Res.
– volume: 54
  start-page: 143
  year: 2004
  ident: D3RA04309F/cit90/1
  publication-title: Acta Pharm.
– volume: 51
  start-page: 869
  year: 2015
  ident: D3RA04309F/cit64/1
  publication-title: Chem. Heterocycl. Compd.
  doi: 10.1007/s10593-015-1789-z
– volume: 100
  start-page: 18
  year: 2015
  ident: D3RA04309F/cit85/1
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2015.05.037
– volume: 8
  start-page: 4182
  year: 2017
  ident: D3RA04309F/cit103/1
  publication-title: J. Mater. Environ. Sci.
– volume: 51
  start-page: 838
  year: 2003
  ident: D3RA04309F/cit16a/1
  publication-title: Chem. Pharm. Bull.
  doi: 10.1248/cpb.51.838
– volume: 6
  start-page: 59375
  year: 2016
  ident: D3RA04309F/cit55/1
  publication-title: RSC Adv.
  doi: 10.1039/C6RA06093E
– start-page: 1
  year: 2003
  ident: D3RA04309F/cit10/1
  publication-title: Rev. Environ. Contam. Toxicol.
– volume: 25
  start-page: 9
  year: 2012
  ident: D3RA04309F/cit35/1
  publication-title: BioMetals
  doi: 10.1007/s10534-011-9496-4
– volume: 79
  start-page: 1743
  year: 2023
  ident: D3RA04309F/cit60/1
  publication-title: Pest Manage. Sci.
  doi: 10.1002/ps.7349
– volume: 9
  start-page: 10
  year: 2018
  ident: D3RA04309F/cit99/1
  publication-title: Proceedings (MDPI)
– volume: 51
  start-page: 838
  year: 2003
  ident: D3RA04309F/cit20/1
  publication-title: Chem. Pharm. Bull.
  doi: 10.1248/cpb.51.838
– volume: 74
  start-page: 2253
  year: 2016
  ident: D3RA04309F/cit7/1
  publication-title: Water Sci. Technol.
  doi: 10.2166/wst.2016.414
– volume: 11
  start-page: 76
  year: 2006
  ident: D3RA04309F/cit25b/1
  publication-title: Arkivoc
  doi: 10.3998/ark.5550190.0007.b07
– volume: 1
  start-page: 1
  year: 2020
  ident: D3RA04309F/cit71/1
  publication-title: Chem. Process.
– volume: 48
  start-page: 2881
  year: 2016
  ident: D3RA04309F/cit97/1
  publication-title: Synthesis
  doi: 10.1055/s-0035-1561459
– volume: 49
  start-page: 355
  year: 2017
  ident: D3RA04309F/cit73/1
  publication-title: Org. Prep. Proced. Int.
  doi: 10.1080/00304948.2017.1342511
– start-page: 2078
  year: 2018
  ident: D3RA04309F/cit81/1
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201800249
– volume: 57
  start-page: 1692
  year: 2020
  ident: D3RA04309F/cit43/1
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.3894
– volume: 88
  start-page: 1103
  year: 2018
  ident: D3RA04309F/cit88/1
  publication-title: Russ. J. Gen. Chem.
  doi: 10.1134/S1070363218060099
– volume: 7
  start-page: 361
  year: 2015
  ident: D3RA04309F/cit41/1
  publication-title: J. Chem. Pharm. Res.
– volume: 50
  start-page: 5183
  year: 2007
  ident: D3RA04309F/cit21/1
  publication-title: J. Med. Chem.
  doi: 10.1021/jm070528f
– volume: 2
  start-page: 179
  year: 2003
  ident: D3RA04309F/cit16b/1
  publication-title: Nat. Rev. Drug. Discov.
  doi: 10.1038/nrd1034
– volume: 5
  start-page: 21498
  year: 2018
  ident: D3RA04309F/cit108/1
  publication-title: Mater. Today: Proc.
  doi: 10.1016/j.matpr.2018.06.560
– volume: 86
  start-page: 420
  year: 2014
  ident: D3RA04309F/cit96/1
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2014.09.001
– volume: 16
  start-page: 3059
  year: 2008
  ident: D3RA04309F/cit22b/1
  publication-title: Bioorg. Med. Chem.
  doi: 10.1016/j.bmc.2007.12.033
– volume: 35
  start-page: 2819
  year: 2005
  ident: D3RA04309F/cit75/1
  publication-title: Synth. Commun.
  doi: 10.1080/00397910500290573
– volume: 1180
  start-page: 227
  year: 2019
  ident: D3RA04309F/cit83/1
  publication-title: J. Mol. Struct.
  doi: 10.1016/j.molstruc.2018.11.030
– volume: 1
  start-page: 126
  year: 2011
  ident: D3RA04309F/cit33/1
  publication-title: Afr. J. Chem. Educ.
– volume: 67
  start-page: 7195
  year: 2011
  ident: D3RA04309F/cit92/1
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2011.06.040
– volume: 29
  start-page: 1
  year: 2022
  ident: D3RA04309F/cit37/1
  publication-title: J. Polym. Res.
  doi: 10.1007/s10965-021-02672-1
– volume: 8
  start-page: 128
  year: 2021
  ident: D3RA04309F/cit65/1
  publication-title: Int. J. Adv. Appl. Sci.
  doi: 10.21833/ijaas.2021.06.015
– volume: 21
  start-page: 1
  year: 2013
  ident: D3RA04309F/cit77/1
  publication-title: Saudi Pharm. J.
  doi: 10.1016/j.jsps.2012.03.002
– volume: 121
  start-page: 158
  year: 2016
  ident: D3RA04309F/cit29/1
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2016.05.043
– volume: 20
  start-page: 577
  year: 2016
  ident: D3RA04309F/cit6/1
  publication-title: J. Saudi Chem. Soc.
  doi: 10.1016/j.jscs.2014.12.004
– volume: 44
  start-page: 645
  year: 2015
  ident: D3RA04309F/cit89/1
  publication-title: Chem. Lett.
  doi: 10.1246/cl.150133
– volume: 5
  start-page: 1
  year: 2017
  ident: D3RA04309F/cit14/1
  publication-title: Cochrane Database Syst. Rev.
– start-page: 353
  year: 2020
  ident: D3RA04309F/cit5/1
  publication-title: Res. Int. Advancem. Plant Sci.
– volume: 41
  start-page: 100930
  year: 2022
  ident: D3RA04309F/cit57/1
  publication-title: Chem. Data Collect.
  doi: 10.1016/j.cdc.2022.100930
– volume: 43
  start-page: 1909
  year: 2017
  ident: D3RA04309F/cit76/1
  publication-title: Res. Chem. Intermed.
  doi: 10.1007/s11164-016-2738-x
– start-page: 1136
  year: 2020
  ident: D3RA04309F/cit104/1
  publication-title: Molbank
  doi: 10.3390/M1136
– volume: 43
  start-page: 1971
  year: 2008
  ident: D3RA04309F/cit9/1
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2007.12.006
– volume: M1011
  start-page: 1
  year: 2018
  ident: D3RA04309F/cit40/1
  publication-title: Molbank
– volume: 40
  start-page: 243
  year: 2019
  ident: D3RA04309F/cit72/1
  publication-title: Bull. Korean Chem. Soc.
  doi: 10.1002/bkcs.11673
– volume: 9
  start-page: 650
  year: 2020
  ident: D3RA04309F/cit42/1
  publication-title: Antibiotics
  doi: 10.3390/antibiotics9100650
– volume: 73
  start-page: 8317
  year: 2008
  ident: D3RA04309F/cit2/1
  publication-title: J. Org. Chem.
  doi: 10.1021/jo801492k
– volume: 65
  start-page: 1
  year: 2022
  ident: D3RA04309F/cit84/1
  publication-title: Egypt. J. Chem.
– volume: 58
  start-page: 6895
  year: 2010
  ident: D3RA04309F/cit18/1
  publication-title: J. Agric. Food Chem.
  doi: 10.1021/jf100872f
– volume: 9
  start-page: 1738
  year: 2020
  ident: D3RA04309F/cit38/1
  publication-title: World J. Pharm. Pharm. Sci.
– volume: 45
  start-page: 944
  year: 2015
  ident: D3RA04309F/cit53/1
  publication-title: Synth. Commun.
  doi: 10.1080/00397911.2014.994128
– volume: 2
  start-page: 1
  year: 2012
  ident: D3RA04309F/cit23/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.9734/ACSJ/2012/1063
– volume: 39
  start-page: 869
  year: 2002
  ident: D3RA04309F/cit27/1
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.5570390503
– volume: 89
  start-page: 1202
  year: 2019
  ident: D3RA04309F/cit61/1
  publication-title: Russ. J. Gen. Chem.
  doi: 10.1134/S1070363219060161
– volume: 7
  start-page: 888
  year: 2007
  ident: D3RA04309F/cit87/1
  publication-title: Mini-Rev. Med. Chem.
  doi: 10.2174/138955707781662645
– volume: 64
  start-page: 5246
  year: 2008
  ident: D3RA04309F/cit74/1
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2008.03.038
– volume: 90
  start-page: 497
  year: 2015
  ident: D3RA04309F/cit30/1
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2014.11.042
– volume: 127
  start-page: 275
  year: 2017
  ident: D3RA04309F/cit32/1
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2016.12.059
– volume: 44
  start-page: 2601
  year: 2001
  ident: D3RA04309F/cit17/1
  publication-title: J. Med. Chem.
  doi: 10.1021/jm010032c
– volume: 12
  start-page: 1689
  year: 2015
  ident: D3RA04309F/cit59/1
  publication-title: World J. Pharm. Res.
– volume: 71
  start-page: 713
  year: 2007
  ident: D3RA04309F/cit24/1
  publication-title: J. Serb. Chem. Soc.
  doi: 10.2298/JSC0607713C
– volume: 9
  start-page: 1004
  year: 2011
  ident: D3RA04309F/cit82/1
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/C0OB00771D
– volume: 60
  start-page: 119
  year: 1927
  ident: D3RA04309F/cit3/1
  publication-title: Ber. Dtsch. Chem. Ges.
  doi: 10.1002/cber.19270600118
– volume: 42
  start-page: 934
  year: 2007
  ident: D3RA04309F/cit25a/1
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2006.12.032
– volume: 7
  start-page: 267
  year: 2023
  ident: D3RA04309F/cit56/1
  publication-title: Chem. Methodol.
– volume: 335
  start-page: 213
  year: 2002
  ident: D3RA04309F/cit28/1
  publication-title: Arch. Pharm.
  doi: 10.1002/1521-4184(200205)335:5<213::AID-ARDP213>3.0.CO;2-H
– volume: 55
  start-page: 1504
  year: 2019
  ident: D3RA04309F/cit66/1
  publication-title: Russ. J. Org. Chem.
  doi: 10.1134/S1070428019100087
– volume: 57
  start-page: 1346
  year: 2016
  ident: D3RA04309F/cit50/1
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2016.02.045
– volume: 51
  start-page: 2928
  year: 2010
  ident: D3RA04309F/cit91/1
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2010.03.117
– volume: 21
  start-page: 487
  year: 1984
  ident: D3RA04309F/cit15/1
  publication-title: Pharmacol. Biochem. Behav.
  doi: 10.1016/S0091-3057(84)80027-1
– volume: 30
  start-page: 123
  year: 2020
  ident: D3RA04309F/cit54/1
  publication-title: Indian J. Heterocycl. Chem.
– volume: 47
  start-page: 463
  year: 2010
  ident: D3RA04309F/cit93/1
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.338
– volume: 26
  start-page: 2907
  year: 2021
  ident: D3RA04309F/cit100/1
  publication-title: Molecules
  doi: 10.3390/molecules26102907
– volume: 15
  start-page: 2619
  year: 2016
  ident: D3RA04309F/cit110/1
  publication-title: Trop. J. Pharm. Res.
  doi: 10.4314/tjpr.v15i12.12
– volume: 26
  start-page: 690
  year: 2016
  ident: D3RA04309F/cit49/1
  publication-title: Bioorg. Med. Chem. Lett.
  doi: 10.1016/j.bmcl.2015.11.038
– volume: 51
  start-page: 142
  year: 2008
  ident: D3RA04309F/cit22a/1
  publication-title: J. Med. Chem.
  doi: 10.1021/jm070821f
– volume: 2
  start-page: 777
  year: 1991
  ident: D3RA04309F/cit1/1
  publication-title: Compr. Org. Synth.
  doi: 10.1016/B978-0-08-052349-1.00049-4
– volume: 11
  start-page: 183
  year: 2018
  ident: D3RA04309F/cit62/1
  publication-title: Int. J. ChemTech Res.
– volume: 57
  start-page: 796
  year: 2020
  ident: D3RA04309F/cit39/1
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.3824
– volume: 76
  start-page: 2880
  year: 2011
  ident: D3RA04309F/cit70/1
  publication-title: J. Org. Chem.
  doi: 10.1021/jo101949y
– volume: 50
  start-page: 1641
  year: 2020
  ident: D3RA04309F/cit106/1
  publication-title: Synth. Commun.
  doi: 10.1080/00397911.2020.1750033
– volume: 4
  start-page: 172
  year: 2016
  ident: D3RA04309F/cit52/1
  publication-title: Indian J. Adv. Chem. Sci.
– volume: 2
  start-page: 635
  year: 2017
  ident: D3RA04309F/cit11/1
  publication-title: Eur. Rev. Med. Pharmacol. Sci.
– volume: 79
  start-page: 153297
  year: 2021
  ident: D3RA04309F/cit107/1
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2021.153297
– volume: 17
  start-page: 2204
  year: 2019
  ident: D3RA04309F/cit78/1
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/C8OB03040E
– volume: 57
  start-page: 1123
  year: 2020
  ident: D3RA04309F/cit46/1
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.3849
– volume: 21
  start-page: 9
  year: 2018
  ident: D3RA04309F/cit63/1
  publication-title: C. R. Chim.
  doi: 10.1016/j.crci.2017.12.001
– start-page: 137
  year: 2006
  ident: D3RA04309F/cit25c/1
  publication-title: Arkivoc
  doi: 10.3998/ark.5550190.0007.a17
– volume: 19
  start-page: 297
  year: 1980
  ident: D3RA04309F/cit34/1
  publication-title: Indian J. Chem.
– volume: 91
  start-page: 246
  year: 2017
  ident: D3RA04309F/cit69/1
  publication-title: Russ. J. Phys. Chem. A
  doi: 10.1134/S0036024417020182
– volume: 53
  start-page: 1347
  year: 2016
  ident: D3RA04309F/cit45/1
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.1506
– volume: 10
  start-page: 487
  year: 2020
  ident: D3RA04309F/cit101/1
  publication-title: Technology
– volume: 1
  start-page: 85
  year: 2005
  ident: D3RA04309F/cit102/1
  publication-title: Synthesis
– volume: 53
  start-page: 62
  year: 2017
  ident: D3RA04309F/cit48/1
  publication-title: Russ. J. Org. Chem.
  doi: 10.1134/S1070428017010110
– volume: 25
  start-page: 2758
  year: 2020
  ident: D3RA04309F/cit44/1
  publication-title: Molecules
  doi: 10.3390/molecules25122758
– volume: 2398
  start-page: 30004
  year: 2022
  ident: D3RA04309F/cit94/1
  publication-title: AIP Conf. Proc.
  doi: 10.1063/5.0093601
– start-page: 1
  year: 2019
  ident: D3RA04309F/cit58/1
  publication-title: Org. Chem.
– volume: 52
  start-page: 307
  year: 2004
  ident: D3RA04309F/cit8/1
  publication-title: Chem. Pharm. Bull.
  doi: 10.1248/cpb.52.307
– volume: 34
  start-page: 102023
  year: 2022
  ident: D3RA04309F/cit95/1
  publication-title: J. King Saud Univ., Sci.
  doi: 10.1016/j.jksus.2022.102023
– start-page: 1
  year: 2021
  ident: D3RA04309F/cit79/1
  publication-title: J. Chem.
  doi: 10.1155/2021/2408006
– volume: 3
  start-page: 52
  year: 2017
  ident: D3RA04309F/cit80/1
  publication-title: Org. Med. Chem. Int. J.
– volume: 8
  start-page: 1
  year: 2010
  ident: D3RA04309F/cit13/1
  publication-title: Cochrane Database Syst. Rev.
– start-page: 641
  year: 2000
  ident: D3RA04309F/cit67/1
  publication-title: Kirk-Othmer Encycl. Chem. Technol.
– volume: 20
  start-page: 255
  year: 2017
  ident: D3RA04309F/cit31/1
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2017.04.002
– volume: 76
  start-page: 2615
  year: 2022
  ident: D3RA04309F/cit68/1
  publication-title: Chem. Pap.
  doi: 10.1007/s11696-022-02066-7
– volume: 42
  start-page: 373
  year: 2007
  ident: D3RA04309F/cit26/1
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2006.09.006
– volume: 152
  start-page: 95
  year: 2021
  ident: D3RA04309F/cit105/1
  publication-title: Monatsh. Chem.
  doi: 10.1007/s00706-020-02733-z
– volume: 49
  start-page: 6027
  year: 2006
  ident: D3RA04309F/cit19/1
  publication-title: J. Med. Chem.
  doi: 10.1021/jm060499t
– volume: 44
  start-page: 153
  year: 1999
  ident: D3RA04309F/cit12/1
  publication-title: Surv. Ophthalmol.
  doi: 10.1016/S0039-6257(99)00079-X
– volume: 87
  start-page: 2454
  year: 2017
  ident: D3RA04309F/cit47/1
  publication-title: Russ. J. Gen. Chem.
  doi: 10.1134/S1070363217100280
– volume: 55
  start-page: 2507
  year: 2018
  ident: D3RA04309F/cit51/1
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.3282
– volume: 97
  start-page: 786
  year: 2015
  ident: D3RA04309F/cit36/1
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2014.11.059
– volume: 49
  start-page: 2971
  year: 2017
  ident: D3RA04309F/cit98/1
  publication-title: Synthesis
  doi: 10.1055/s-0036-1588992
– volume: 60
  start-page: 819
  year: 2017
  ident: D3RA04309F/cit109/1
  publication-title: Sci. China Mater.
  doi: 10.1007/s40843-017-9084-x
– volume: 1
  start-page: 1
  year: 2011
  ident: D3RA04309F/cit4/1
  publication-title: Mod. Heterocycl. Chem.
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Snippet The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier-Haack (V....
The aim of this review is to encapsulate the synthetic protocols and medicinal aspects of a wide range of heterocyclic compounds using the Vilsmeier–Haack (V....
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SubjectTerms Anticonvulsants
Chemical synthesis
Chemistry
Heterocyclic compounds
Organic chemistry
Precursors
Reagents
Title Unravelling the synthetic and therapeutic aspects of five, six and fused heterocycles using Vilsmeier-Haack reagent
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https://pubmed.ncbi.nlm.nih.gov/PMC10478505
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