Paraldehyde as an Acetaldehyde Precursor in Asymmetric Michael Reactions Promoted by Site-Isolated Incompatible Catalysts
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| Vydané v: | Chemistry : a European journal Ročník 19; číslo 33; s. 10814 - 10817 |
|---|---|
| Hlavní autori: | , , , |
| Médium: | Journal Article |
| Jazyk: | English |
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Weinheim
WILEY-VCH Verlag
12.08.2013
Wiley |
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| ISSN: | 0947-6539, 1521-3765, 1521-3765 |
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| Author | Rodríguez-Escrich, Carles Sayalero, Sonia Pericàs, Miquel A. Fan, Xinyuan |
|---|---|
| Author_xml | – sequence: 1 givenname: Xinyuan surname: Fan fullname: Fan, Xinyuan organization: Institute of Chemical Research of Catalonia (ICIQ), Av. Països Catalans, 16, 43007 Tarragona (Spain), Fax: (+34) 977-920-243 – sequence: 2 givenname: Carles surname: Rodríguez-Escrich fullname: Rodríguez-Escrich, Carles organization: Institute of Chemical Research of Catalonia (ICIQ), Av. Països Catalans, 16, 43007 Tarragona (Spain), Fax: (+34) 977-920-243 – sequence: 3 givenname: Sonia surname: Sayalero fullname: Sayalero, Sonia organization: Institute of Chemical Research of Catalonia (ICIQ), Av. Països Catalans, 16, 43007 Tarragona (Spain), Fax: (+34) 977-920-243 – sequence: 4 givenname: Miquel A. surname: Pericàs fullname: Pericàs, Miquel A. email: mapericas@iciq.es organization: Institute of Chemical Research of Catalonia (ICIQ), Av. Països Catalans, 16, 43007 Tarragona (Spain), Fax: (+34) 977-920-243 |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23821520$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1021/ol802438u 10.1002/anie.200801130 10.1002/ange.200704870 10.1002/anie.200704870 10.1002/chem.201101730 10.1002/anie.200806049 10.1002/1521-3773(20010105)40:1<74::AID-ANIE74>3.0.CO;2-C 10.1002/ange.200704684 10.1038/nature06740 10.1002/anie.200504353 10.1002/adsc.200900817 10.1002/anie.200704684 10.1021/ja203660r 10.1038/nature07367 10.1021/ja300415t 10.1002/ange.200705523 10.1002/ange.200801130 10.1002/ange.200802073 10.1021/ja9068112 10.1002/ejoc.201101157 10.1039/c2cc38370e 10.1021/cr0684016 10.1002/anie.200802073 10.1021/jp7096845 10.1002/anie.200462101 10.1002/anie.200502095 10.1002/chem.200800094 10.1002/ange.200462101 10.1002/ejoc.201100267 10.1002/anie.200705523 10.1002/anie.200805628 10.1002/ange.200502095 10.1002/ange.200800847 10.1021/ja8013456 10.1002/ange.200703002 10.1002/anie.201201347 10.1021/jo200991q 10.1021/jo900570y 10.1002/ange.200805628 10.1002/anie.200500599 10.1002/anie.200801231 10.1002/ange.200702210 10.1002/ange.200504353 10.1002/1521-3757(20010105)113:1<76::AID-ANGE76>3.0.CO;2-F 10.1002/anie.201107404 10.1002/chem.201100388 10.1177/30.2.6174561 10.1002/ange.200500599 10.1002/adsc.201200887 10.1002/ange.200801231 10.1021/ol202340p 10.1002/anie.200800847 10.1002/anie.200702210 10.1002/ange.200806049 10.1002/anie.200703002 10.1002/adsc.201200215 10.1002/hlca.201200283 10.1055/s-0030-1259528 |
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| Keywords | EFFICIENT ORGANOCATALYSTS ENAMINE CATALYSIS ALDEHYDES organocatalysts paraldehyde AMINO SULFONAMIDE DIARYLPROLINOL ALDOL REACTION acetaldehyde NITRO-OLEFINS STAR POLYMERS DIPHENYLPROLINOL SILYL ETHERS Michael reaction site isolation DOUBLE-MANNICH REACTION |
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| References | V. Coeffard, A. Desmarchelier, B. Morel, X. Moreau, C. Greck, Org. Lett. 2011, 13, 5778-5781 Angew. Chem. Int. Ed. 2006, 45, 4238-4240 E. Alza, S. Sayalero, X. C. Cambeiro, R. Martin-Rapún, P. O. Miranda, M. A. Pericàs, Synlett 2011, 464-468. Y. Hayashi, T. Itoh, M. Ohkubo, H. Ishikawa, Angew. Chem. 2008, 120, 4800-4802 Angew. Chem. Int. Ed. 2008, 47, 2082-2084 K. L. Jensen, G. Dickmeiss, H. Jiang, Ł. Albrecht, K. A. Jørgensen, Acc. Chem. Res. 2011, 44, 248-264. For a study on the effect of water in the Michael addition of aldehydes to nitrostyrenes mediated by a tripeptide, see: M. Wiesner, G. Upert, G. Angelini, H. Wennemers, J. Am. Chem. Soc. 2010, 132, 6-7. Y. Qiao, J. He, B. Ni, A. D. Headley, Adv. Synth. Catal. 2012, 354, 2849-2853. E. Arceo, P. Melchiorre, Angew. Chem. Int. Ed. 2012, 51, 5290-5292. J. W. Yang, C. Chandler, M. Stadler, D. Kampen, B. List, Nature 2008, 452, 453-455 Angew. Chem. Int. Ed. 2009, 48, 1838-1840 E. Zandvoort, E. M. Geertsema, B.-J. Baas, W. J. Quax, G. J. Poelarends, Angew. Chem. Int. Ed. 2012, 51, 1240-1243. G. S. Nettleton, J. Histochem. Cytochem. 1982, 30, 175-178. M. Marigo, T. C. Wabnitz, D. Fielenbach, K. A. Jørgensen, Angew. Chem. 2005, 117, 804-807 For a highlight on the pioneering acetaldehyde organocatalytic reactions, see: B. Alcaide, P. Almendros, Angew. Chem. 2008, 120, 4710-4712 B. Helms, S. J. Guillaudeu, Y. Xie, M. McMurdo, C. J. Hawker, J. M. J. Fréchet, Angew. Chem. 2005, 117, 6542-6545 A. L. Miller II, N. B. Bowden, J. Org. Chem. 2009, 74, 4834-4840. Y. Chi, S. T. Scroggins, J. M. J. Fréchet, J. Am. Chem. Soc. 2008, 130, 6322-6323. C. F. Barbas III, Angew. Chem. 2008, 120, 44-50 A. Dondoni, A. Massi, Angew. Chem. 2008, 120, 4716-4739 Angew. Chem. Int. Ed. 2008, 47, 935-939 J. Burés, A. Armstrong, D. G. Blackmond, J. Am. Chem. Soc. 2011, 133, 8822-8825 P. Melchiorre, M. Marigo, A. Carlone, G. Bartoli, Angew. Chem. 2008, 120, 6232-6265 Angew. Chem. Int. Ed. 2001, 40, 74-91 Y. Hayashi, S. Samanta, T. Itoh, H. Ishikawa, Org. Lett. 2008, 10, 5581-5583 B. Nozière, A. Córdova, J. Phys. Chem. A 2008, 112, 2827-2837 Angew. Chem. Int. Ed. 2008, 47, 9053-9058 D. Seebach, X. Sun, C. Sparr, M.-O. Ebert, W. B. Schweizer, A. K. Beck, Helv. Chim. Acta 2012, 95, 1064-1078. E. Alza, M. A. Pericàs, Adv. Synth. Catal. 2009, 351, 3051-3056 Angew. Chem. Int. Ed. 2008, 47, 4719-4721. Angew. Chem. Int. Ed. 2008, 47, 6138-6171 The oxidative deactivation of Jørgensen-Hayashi-type catalysts in the Michael addition of nitromethane to cinnamaldehyde has been recently reported: O. V. Maltsev, A. O. Chizhov, S. G. Zlotin, Chem. Eur. J. 2011, 17, 6109-6117. Angew. Chem. Int. Ed. 2008, 47, 4632-4634. Angew. Chem. Int. Ed. 2005, 44, 794-797 Y. Hayashi, T. Itoh, S. Aratake, H. Ishikawa, Angew. Chem. 2008, 120, 2112-2114 D. W. C. MacMillan, Nature 2008, 455, 304-308 M. T. Mwangi, M. B. Runge, K. M. Hoak, M. D. Schulz, N. B. Bowden, Chem. Eur. J. 2008, 14, 6780-6788 D. B. Ramachary, Y. V. Reddy, Eur. J. Org. Chem. 2012, 865-887 X. Fan, S. Sayalero, M. A. Pericàs, Adv. Synth. Catal. 2012, 354, 2971-2976; for a closely related supported catalyst protected with TMS, see C. Chandler, P. Galzerano, A. Michrowska, B. List, Angew. Chem. 2009, 121, 2012-2014 S. Mukherjee, J.-W. Yang, S. Hoffmann, B. List, Chem. Rev. 2007, 107, 5471 Angew. Chem. Int. Ed. 2008, 47, 42-47 Angew. Chem. Int. Ed. 2005, 44, 4212-4215; for a recent account on the diarylprolinol silyl ether system, see Y. Hayashi, H. Gotoh, T. Hayashi, M. Shoji, Angew. Chem. 2005, 117, 4284-4287 M. B. Runge, M. T. Mwangi, A. L. Miller, M. Perring, N. B. Bowden, Angew. Chem. 2008, 120, 949-953 F. A. Long, J. W. Howard, Org. Synth. 1943, Coll. Vol. 2, 87 B. Voit, Angew. Chem. 2006, 118, 4344-4346 E. Alza, S. Sayalero, P. Kasaplar, D. Almasi, M. A. Pericàs, Chem. Eur. J. 2011, 17, 11585-11595 Angew. Chem. Int. Ed. 2008, 47, 4722-4724. Angew. Chem. Int. Ed. 2005, 44, 6384-6387 T. Kano, R. Sakamoto, Y. Yamaguchi, K.-i. Itoh, K. Maruoka, Chem. Commun. 2013, 49, 1118-1120. S. Hecht, J. M. J. Fréchet, Angew. Chem. 2001, 113, 76-94 Y. Hayashi, T. Okano, T. Itoh, T. Urushima, H. Ishikawa, T. Uchimaru, Angew. Chem. 2008, 120, 9193-9198 Angew. Chem. Int. Ed. 2008, 47, 4638-4660 K. I. Jentzsch, T. Min, J. I. Etcheson, J. C. Fettinger, A. K. Franz, J. Org. Chem. 2011, 76, 7065-7075. Angew. Chem. Int. Ed. 2009, 48, 1978-1980 P. García-García, A. Ladépêche, R. Halder, B. List, Angew. Chem. 2008, 120, 4797-4799 S. Hu, L. Zhang, J. Li, S. Luo, J.-P. Cheng, Eur. J. Org. Chem. 2011, 3347-3352. J. Burés, A. Armstrong, D. G. Blackmond, J. Am. Chem. Soc. 2012, 134, 6741-6750 T. Kano, Y. Yamaguchi, K. Maruoka, Angew. Chem. 2009, 121, 1870-1872 e_1_2_4_40_2 e_1_2_4_42_3 e_1_2_4_44_2 e_1_2_4_40_3 e_1_2_4_21_2 e_1_2_4_42_2 e_1_2_4_23_3 e_1_2_4_23_2 e_1_2_4_48_2 e_1_2_4_25_3 e_1_2_4_25_2 e_1_2_4_46_2 e_1_2_4_27_2 e_1_2_4_29_2 e_1_2_4_1_2 e_1_2_4_3_2 e_1_2_4_5_3 Alza E. (e_1_2_4_50_2) 2011 e_1_2_4_5_2 e_1_2_4_7_2 e_1_2_4_9_3 e_1_2_4_9_2 e_1_2_4_31_2 e_1_2_4_54_2 e_1_2_4_10_2 e_1_2_4_33_2 e_1_2_4_52_2 e_1_2_4_10_3 e_1_2_4_12_2 e_1_2_4_35_2 e_1_2_4_14_2 e_1_2_4_37_2 e_1_2_4_14_3 e_1_2_4_39_2 e_1_2_4_16_2 e_1_2_4_18_2 e_1_2_4_39_3 e_1_2_4_20_2 e_1_2_4_43_2 e_1_2_4_22_2 e_1_2_4_41_2 e_1_2_4_41_3 e_1_2_4_24_2 e_1_2_4_47_2 e_1_2_4_26_2 e_1_2_4_45_2 e_1_2_4_24_3 e_1_2_4_28_2 e_1_2_4_49_2 e_1_2_4_2_2 e_1_2_4_4_2 e_1_2_4_6_2 e_1_2_4_4_3 e_1_2_4_8_2 Long F. A. (e_1_2_4_36_2) 1943 e_1_2_4_6_3 e_1_2_4_51_2 e_1_2_4_30_2 e_1_2_4_55_2 e_1_2_4_11_2 e_1_2_4_32_2 e_1_2_4_53_2 e_1_2_4_11_3 e_1_2_4_13_2 e_1_2_4_34_2 e_1_2_4_13_3 e_1_2_4_17_2 Jensen K. L. (e_1_2_4_15_2) 2011; 44 e_1_2_4_38_2 e_1_2_4_19_2 e_1_2_4_17_3 Burés, J (WOS:000291667600013) 2011; 133 Garcia-Garcia, P. (000322626500009.30) 2008; 120 (000322626500009.2) 2006; 45 Yang, JW (WOS:000254341300027) 2008; 452 Alza, E (WOS:000287575400004) 2011 Arceo, E (WOS:000304345800004) 2012; 51 Jensen, K. L. 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| References_xml | – reference: Angew. Chem. Int. Ed. 2008, 47, 4719-4721. – reference: F. A. Long, J. W. Howard, Org. Synth. 1943, Coll. Vol. 2, 87; – reference: Angew. Chem. Int. Ed. 2008, 47, 4722-4724. – reference: Angew. Chem. Int. Ed. 2009, 48, 1838-1840; – reference: G. S. Nettleton, J. Histochem. Cytochem. 1982, 30, 175-178. – reference: P. Melchiorre, M. Marigo, A. Carlone, G. Bartoli, Angew. Chem. 2008, 120, 6232-6265; – reference: Angew. Chem. Int. Ed. 2008, 47, 6138-6171; – reference: K. I. Jentzsch, T. Min, J. I. Etcheson, J. C. Fettinger, A. K. Franz, J. Org. Chem. 2011, 76, 7065-7075. – reference: D. B. Ramachary, Y. V. Reddy, Eur. J. Org. Chem. 2012, 865-887; – reference: Angew. Chem. Int. Ed. 2001, 40, 74-91; – reference: Y. Hayashi, T. Itoh, M. Ohkubo, H. Ishikawa, Angew. Chem. 2008, 120, 4800-4802; – reference: E. Alza, S. Sayalero, P. Kasaplar, D. Almasi, M. A. Pericàs, Chem. Eur. J. 2011, 17, 11585-11595; – reference: S. Hu, L. Zhang, J. Li, S. Luo, J.-P. Cheng, Eur. J. Org. Chem. 2011, 3347-3352. – reference: J. W. Yang, C. Chandler, M. Stadler, D. Kampen, B. List, Nature 2008, 452, 453-455; – reference: C. F. Barbas III, Angew. Chem. 2008, 120, 44-50; – reference: T. Kano, R. Sakamoto, Y. Yamaguchi, K.-i. Itoh, K. Maruoka, Chem. Commun. 2013, 49, 1118-1120. – reference: Angew. Chem. Int. Ed. 2006, 45, 4238-4240; – reference: M. T. Mwangi, M. B. Runge, K. M. Hoak, M. D. Schulz, N. B. Bowden, Chem. Eur. J. 2008, 14, 6780-6788; – reference: K. L. Jensen, G. Dickmeiss, H. Jiang, Ł. Albrecht, K. A. Jørgensen, Acc. Chem. Res. 2011, 44, 248-264. – reference: X. Fan, S. Sayalero, M. A. Pericàs, Adv. Synth. Catal. 2012, 354, 2971-2976; for a closely related supported catalyst protected with TMS, see: – reference: D. Seebach, X. Sun, C. Sparr, M.-O. Ebert, W. B. Schweizer, A. K. Beck, Helv. Chim. Acta 2012, 95, 1064-1078. – reference: Angew. Chem. Int. Ed. 2005, 44, 794-797; – reference: Angew. Chem. Int. Ed. 2008, 47, 4632-4634. – reference: Angew. Chem. Int. Ed. 2008, 47, 4638-4660; – reference: B. Voit, Angew. Chem. 2006, 118, 4344-4346; – reference: Y. Qiao, J. He, B. Ni, A. D. Headley, Adv. Synth. Catal. 2012, 354, 2849-2853. – reference: E. Zandvoort, E. M. Geertsema, B.-J. Baas, W. J. Quax, G. J. Poelarends, Angew. Chem. Int. Ed. 2012, 51, 1240-1243. – reference: A. Dondoni, A. Massi, Angew. Chem. 2008, 120, 4716-4739; – reference: E. Alza, S. Sayalero, X. C. Cambeiro, R. Martin-Rapún, P. O. Miranda, M. A. Pericàs, Synlett 2011, 464-468. – reference: P. García-García, A. Ladépêche, R. Halder, B. List, Angew. Chem. 2008, 120, 4797-4799; – reference: M. Marigo, T. C. Wabnitz, D. Fielenbach, K. A. Jørgensen, Angew. Chem. 2005, 117, 804-807; – reference: J. Burés, A. Armstrong, D. G. Blackmond, J. Am. Chem. Soc. 2012, 134, 6741-6750; – reference: For a study on the effect of water in the Michael addition of aldehydes to nitrostyrenes mediated by a tripeptide, see: M. Wiesner, G. Upert, G. Angelini, H. Wennemers, J. Am. Chem. Soc. 2010, 132, 6-7. – reference: D. W. C. MacMillan, Nature 2008, 455, 304-308; – reference: C. Chandler, P. Galzerano, A. Michrowska, B. List, Angew. Chem. 2009, 121, 2012-2014; – reference: The oxidative deactivation of Jørgensen-Hayashi-type catalysts in the Michael addition of nitromethane to cinnamaldehyde has been recently reported: O. V. Maltsev, A. O. Chizhov, S. G. Zlotin, Chem. Eur. J. 2011, 17, 6109-6117. – reference: E. Arceo, P. Melchiorre, Angew. Chem. Int. Ed. 2012, 51, 5290-5292. – reference: Angew. Chem. Int. Ed. 2005, 44, 6384-6387; – reference: J. Burés, A. Armstrong, D. G. Blackmond, J. Am. Chem. Soc. 2011, 133, 8822-8825; – reference: Y. Hayashi, H. Gotoh, T. Hayashi, M. Shoji, Angew. Chem. 2005, 117, 4284-4287; – reference: Angew. Chem. Int. Ed. 2008, 47, 2082-2084; – reference: Y. Chi, S. T. Scroggins, J. M. J. Fréchet, J. Am. Chem. Soc. 2008, 130, 6322-6323. – reference: V. Coeffard, A. Desmarchelier, B. Morel, X. Moreau, C. Greck, Org. Lett. 2011, 13, 5778-5781; – reference: B. Nozière, A. Córdova, J. Phys. Chem. A 2008, 112, 2827-2837; – reference: S. Mukherjee, J.-W. Yang, S. Hoffmann, B. List, Chem. Rev. 2007, 107, 5471; – reference: A. L. Miller II, N. B. Bowden, J. Org. Chem. 2009, 74, 4834-4840. – reference: For a highlight on the pioneering acetaldehyde organocatalytic reactions, see: B. Alcaide, P. Almendros, Angew. Chem. 2008, 120, 4710-4712; – reference: Angew. Chem. Int. Ed. 2005, 44, 4212-4215; for a recent account on the diarylprolinol silyl ether system, see: – reference: E. Alza, M. A. Pericàs, Adv. Synth. Catal. 2009, 351, 3051-3056; – reference: Y. Hayashi, S. Samanta, T. Itoh, H. Ishikawa, Org. Lett. 2008, 10, 5581-5583; – reference: M. B. Runge, M. T. Mwangi, A. L. Miller, M. Perring, N. B. Bowden, Angew. Chem. 2008, 120, 949-953; – reference: Y. Hayashi, T. Okano, T. Itoh, T. Urushima, H. Ishikawa, T. Uchimaru, Angew. Chem. 2008, 120, 9193-9198; – reference: B. Helms, S. J. Guillaudeu, Y. Xie, M. McMurdo, C. J. Hawker, J. M. J. Fréchet, Angew. Chem. 2005, 117, 6542-6545; – reference: Y. Hayashi, T. Itoh, S. Aratake, H. Ishikawa, Angew. Chem. 2008, 120, 2112-2114; – reference: Angew. Chem. Int. Ed. 2008, 47, 9053-9058; – reference: Angew. Chem. Int. Ed. 2008, 47, 42-47; – reference: Angew. Chem. Int. Ed. 2009, 48, 1978-1980; – reference: T. Kano, Y. Yamaguchi, K. Maruoka, Angew. Chem. 2009, 121, 1870-1872; – reference: Angew. Chem. Int. Ed. 2008, 47, 935-939; – reference: S. Hecht, J. M. J. Fréchet, Angew. Chem. 2001, 113, 76-94; – ident: e_1_2_4_18_2 doi: 10.1021/ol802438u – ident: e_1_2_4_11_3 doi: 10.1002/anie.200801130 – ident: e_1_2_4_17_2 doi: 10.1002/ange.200704870 – ident: e_1_2_4_17_3 doi: 10.1002/anie.200704870 – ident: e_1_2_4_49_2 doi: 10.1002/chem.201101730 – ident: e_1_2_4_24_3 doi: 10.1002/anie.200806049 – ident: e_1_2_4_39_3 doi: 10.1002/1521-3773(20010105)40:1<74::AID-ANIE74>3.0.CO;2-C – ident: e_1_2_4_5_2 doi: 10.1002/ange.200704684 – ident: e_1_2_4_21_2 – ident: e_1_2_4_22_2 doi: 10.1038/nature06740 – ident: e_1_2_4_41_3 doi: 10.1002/anie.200504353 – volume: 44 start-page: 248 year: 2011 ident: e_1_2_4_15_2 publication-title: Acc. Chem. Res. – ident: e_1_2_4_35_2 – ident: e_1_2_4_48_2 doi: 10.1002/adsc.200900817 – ident: e_1_2_4_5_3 doi: 10.1002/anie.200704684 – ident: e_1_2_4_32_2 doi: 10.1021/ja203660r – ident: e_1_2_4_51_2 – ident: e_1_2_4_3_2 doi: 10.1038/nature07367 – ident: e_1_2_4_46_2 – ident: e_1_2_4_54_2 – ident: e_1_2_4_33_2 doi: 10.1021/ja300415t – ident: e_1_2_4_6_2 doi: 10.1002/ange.200705523 – ident: e_1_2_4_11_2 doi: 10.1002/ange.200801130 – ident: e_1_2_4_23_2 doi: 10.1002/ange.200802073 – ident: e_1_2_4_53_2 doi: 10.1021/ja9068112 – ident: e_1_2_4_7_2 doi: 10.1002/ejoc.201101157 – ident: e_1_2_4_27_2 doi: 10.1039/c2cc38370e – ident: e_1_2_4_2_2 doi: 10.1021/cr0684016 – ident: e_1_2_4_23_3 doi: 10.1002/anie.200802073 – ident: e_1_2_4_19_2 doi: 10.1021/jp7096845 – ident: e_1_2_4_13_3 doi: 10.1002/anie.200462101 – start-page: 87 year: 1943 ident: e_1_2_4_36_2 publication-title: Org. Synth. – ident: e_1_2_4_40_3 doi: 10.1002/anie.200502095 – ident: e_1_2_4_43_2 doi: 10.1002/chem.200800094 – ident: e_1_2_4_13_2 doi: 10.1002/ange.200462101 – ident: e_1_2_4_20_2 doi: 10.1002/ejoc.201100267 – ident: e_1_2_4_6_3 doi: 10.1002/anie.200705523 – ident: e_1_2_4_25_3 doi: 10.1002/anie.200805628 – ident: e_1_2_4_40_2 doi: 10.1002/ange.200502095 – ident: e_1_2_4_10_2 doi: 10.1002/ange.200800847 – ident: e_1_2_4_55_2 – ident: e_1_2_4_45_2 doi: 10.1021/ja8013456 – ident: e_1_2_4_42_2 doi: 10.1002/ange.200703002 – ident: e_1_2_4_8_2 doi: 10.1002/anie.201201347 – ident: e_1_2_4_28_2 doi: 10.1021/jo200991q – ident: e_1_2_4_44_2 doi: 10.1021/jo900570y – ident: e_1_2_4_25_2 doi: 10.1002/ange.200805628 – ident: e_1_2_4_38_2 – ident: e_1_2_4_16_2 – ident: e_1_2_4_14_3 doi: 10.1002/anie.200500599 – ident: e_1_2_4_9_3 doi: 10.1002/anie.200801231 – ident: e_1_2_4_12_2 – ident: e_1_2_4_4_2 doi: 10.1002/ange.200702210 – ident: e_1_2_4_1_2 – ident: e_1_2_4_41_2 doi: 10.1002/ange.200504353 – ident: e_1_2_4_39_2 doi: 10.1002/1521-3757(20010105)113:1<76::AID-ANGE76>3.0.CO;2-F – ident: e_1_2_4_29_2 doi: 10.1002/anie.201107404 – ident: e_1_2_4_52_2 doi: 10.1002/chem.201100388 – ident: e_1_2_4_31_2 – ident: e_1_2_4_37_2 doi: 10.1177/30.2.6174561 – ident: e_1_2_4_14_2 doi: 10.1002/ange.200500599 – ident: e_1_2_4_47_2 doi: 10.1002/adsc.201200887 – ident: e_1_2_4_9_2 doi: 10.1002/ange.200801231 – ident: e_1_2_4_26_2 doi: 10.1021/ol202340p – ident: e_1_2_4_10_3 doi: 10.1002/anie.200800847 – start-page: 464 year: 2011 ident: e_1_2_4_50_2 publication-title: Synlett – ident: e_1_2_4_4_3 doi: 10.1002/anie.200702210 – ident: e_1_2_4_24_2 doi: 10.1002/ange.200806049 – ident: e_1_2_4_42_3 doi: 10.1002/anie.200703002 – ident: e_1_2_4_30_2 doi: 10.1002/adsc.201200215 – ident: e_1_2_4_34_2 doi: 10.1002/hlca.201200283 – volume: 47 start-page: 4632 year: 2008 ident: 000322626500009.12 publication-title: Angew. Chem. Int. Ed. – volume: 452 start-page: 453 year: 2008 ident: WOS:000254341300027 article-title: Proline-catalysed Mannich reactions of acetaldehyde publication-title: NATURE doi: 10.1038/nature06740 – volume: 47 start-page: 2082 year: 2008 ident: 000322626500009.7 publication-title: Angew. Chem. Int. Ed. – volume: 40 start-page: 74 year: 2001 ident: 000322626500009.5 publication-title: Angew. Chem. Int. Ed. – volume: 354 start-page: 2971 year: 2012 ident: WOS:000310879100013 article-title: Asymmetric α-Amination of Aldehydes Catalyzed by PS-Diphenylprolinol Silyl Ethers: Remediation of Catalyst Deactivation for Continuous Flow Operation publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201200887 – volume: 51 start-page: 1240 year: 2012 ident: WOS:000299416600029 article-title: Bridging between Organocatalysis and Biocatalysis: Asymmetric Addition of Acetaldehyde to ß-Nitrostyrenes Catalyzed by a Promiscuous Proline-Based Tautomerase publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201107404 – volume: 120 start-page: 9193 year: 2008 ident: 000322626500009.32 publication-title: Angew. Chem. – volume: 51 start-page: 5290 year: 2012 ident: WOS:000304345800004 article-title: Extending the Aminocatalytic HOMO-Raising Activation Strategy: Where Is the Limit? publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201201347 – volume: 95 start-page: 1064 year: 2012 ident: WOS:000306277000003 article-title: 1,2-Oxazine N-Oxides as Catalyst Resting States in Michael Additions of Aldehydes to Nitro Olefins Organocatalyzed by α,α-Diphenylprolinol Trimethylsilyl Ether publication-title: HELVETICA CHIMICA ACTA doi: 10.1002/hlca.201200283 – volume: 112 start-page: 2827 year: 2008 ident: WOS:000254540800009 article-title: A kinetic and mechanistic study of the amino acid catalyzed aldol condensation of acetaldehyde in aqueous and salt solutions publication-title: JOURNAL OF PHYSICAL CHEMISTRY A doi: 10.1021/jp7096845 – volume: 120 start-page: 4797 year: 2008 ident: 000322626500009.30 publication-title: Angew. Chem. – volume: 47 start-page: 9053 year: 2008 ident: 000322626500009.13 publication-title: Angew. Chem. Int. Ed. – volume: 48 start-page: 1978 year: 2009 ident: 000322626500009.10 publication-title: Angew. Chem. Int. Ed. – volume: 44 start-page: 794 year: 2005 ident: WOS:000226711700024 article-title: Enantioselective organocatalyzed a sulfenylation of aldehydes publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200462101 – volume: 134 start-page: 6741 year: 2012 ident: WOS:000302887300037 article-title: Curtin-Hammett Paradigm for Stereocontrol in Organocatalysis by Diarylprolinol Ether Catalysts publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja300415t – volume: 118 start-page: 4344 year: 2006 ident: 000322626500009.56 publication-title: Angew. Chem. – volume: 44 start-page: 6384 year: 2005 ident: 000322626500009.3 publication-title: Angew. Chem. Int. Ed. – volume: 44 start-page: 4212 year: 2005 ident: 000322626500009.11 publication-title: Angew. Chem. Int. Ed. – volume: 14 start-page: 6780 year: 2008 ident: WOS:000258217000025 article-title: A materials approach to site-isolation of Grubbs catalysts from incompatible solvents and m-chloroperoxybenzoic acid publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.200800094 – volume: 47 start-page: 4719 year: 2008 ident: 000322626500009.14 publication-title: Angew. Chem. Int. Ed. – year: 1943 ident: 000322626500009.43 publication-title: Org. Synth. – volume: 2012 start-page: 865 year: 2012 ident: WOS:000299947300001 article-title: Dienamine Catalysis: An Emerging Technology in Organic Synthesis publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ejoc.201101157 – volume: 47 start-page: 935 year: 2008 ident: 000322626500009.1 publication-title: Angew. Chem. Int. Ed. – volume: 13 start-page: 5778 year: 2011 ident: WOS:000296212200018 article-title: Stereoselective Organocatalytic One-Pot α,α-Bifunctionalization of Acetaldehyde by a Tandem Mannich Reaction/Electrophilic Amination publication-title: ORGANIC LETTERS doi: 10.1021/ol202340p – volume: 47 start-page: 6138 year: 2008 ident: 000322626500009.8 publication-title: Angew. Chem. Int. Ed. – volume: 120 start-page: 4800 year: 2008 ident: 000322626500009.33 publication-title: Angew. Chem. – volume: 107 start-page: 5471 year: 2007 ident: WOS:000251583300003 article-title: Asymmetric enamine catalysis publication-title: CHEMICAL REVIEWS – volume: 10 start-page: 5581 year: 2008 ident: WOS:000261613700021 article-title: Asymmetric, Catalytic, and Direct Self-Aldol Reaction of Acetaldehyde Catalyzed by Diarylprolinol publication-title: ORGANIC LETTERS doi: 10.1021/ol802438u – volume: 133 start-page: 8822 year: 2011 ident: WOS:000291667600013 article-title: Mechanistic Rationalization of Organocatalyzed Conjugate Addition of Linear Aldehydes to Nitro-olefins publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja203660r – volume: 47 start-page: 4722 year: 2008 ident: 000322626500009.16 publication-title: Angew. Chem. Int. Ed. – start-page: 464 year: 2011 ident: WOS:000287575400004 article-title: Catalytic Batch and Continuous Flow Production of Highly Enantioenriched Cyclohexane Derivatives with Polymer-Supported Diarylprolinol Silyl Ethers publication-title: SYNLETT doi: 10.1055/s-0030-1259528 – volume: 120 start-page: 44 year: 2008 ident: 000322626500009.22 publication-title: Angew. Chem. – volume: 120 start-page: 6232 year: 2008 ident: 000322626500009.47 publication-title: Angew. Chem. – volume: 48 start-page: 1838 year: 2009 ident: 000322626500009.9 publication-title: Angew. Chem. Int. Ed. – volume: 121 start-page: 1870 year: 2009 ident: 000322626500009.41 publication-title: Angew. Chem. – volume: 117 start-page: 6542 year: 2005 ident: 000322626500009.37 publication-title: Angew. Chem. – volume: 120 start-page: 949 year: 2008 ident: 000322626500009.54 publication-title: Angew. Chem. – volume: 117 start-page: 4284 year: 2005 ident: 000322626500009.34 publication-title: Angew. Chem. – volume: 117 start-page: 804 year: 2005 ident: 000322626500009.46 publication-title: Angew. Chem. – volume: 17 start-page: 6109 year: 2011 ident: WOS:000291798700013 article-title: Chiral Ionic Liquid/ESI-MS Methodology as an Efficient Tool for the Study of Transformations of Supported Organocatalysts: Deactivation Pathways of Jorgensen-Hayashi-Type Catalysts in Asymmetric Michael Reactions publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201100388 – volume: 354 start-page: 2849 year: 2012 ident: WOS:000309907300034 article-title: Asymmetric Michael Reaction of Acetaldehyde with Nitroolefins Catalyzed by Highly Water-Compatible Organocatalysts in Aqueous Media publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201200215 – volume: 455 start-page: 304 year: 2008 ident: WOS:000259265200030 article-title: The advent and development of organocatalysis publication-title: NATURE doi: 10.1038/nature07367 – volume: 76 start-page: 7065 year: 2011 ident: WOS:000294242900011 article-title: Silyl Fluoride Electrophiles for the Enantioselective Synthesis of Silylated Pyrrolidine Catalysts publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo200991q – volume: 132 start-page: 6 year: 2010 ident: WOS:000275084400003 article-title: Enamine Catalysis with Low Catalyst Loadings - High Efficiency via Kinetic Studies publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja9068112 – volume: 47 start-page: 2082 year: 2008 ident: WOS:000253825200021 article-title: A diarylprolinol in an asymmetric, catalytic, and direct crossed-aldol reaction of acetaldehyde publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200704870 – volume: 351 start-page: 3051 year: 2009 ident: WOS:000273394500003 article-title: A Highly Selective, Polymer-Supported Organocatalyst for Michael Additions with Enzyme-Like Behavior publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.200900817 – volume: 45 start-page: 4238 year: 2006 ident: 000322626500009.2 publication-title: Angew. Chem. Int. Ed. – volume: 130 start-page: 6322 year: 2008 ident: WOS:000255854100011 article-title: One-pot multi-component asymmetric cascade reactions catalyzed by soluble star polymers with highly branched non-interpenetrating catalytic cores publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja8013456 – volume: 47 start-page: 4638 year: 2008 ident: 000322626500009.6 publication-title: Angew. Chem. Int. Ed. – volume: 121 start-page: 2012 year: 2009 ident: 000322626500009.25 publication-title: Angew. Chem. – volume: 17 start-page: 11585 year: 2011 ident: WOS:000297014400028 article-title: Polystyrene-Supported Diarylprolinol Ethers as Highly Efficient Organocatalysts for Michael-Type Reactions publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201101730 – volume: 49 start-page: 1118 year: 2013 ident: WOS:000313340200025 article-title: One-pot cross double-Mannich reaction of acetaldehyde catalyzed by a binaphthyl-based amino sulfonamide publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c2cc38370e – volume: 47 start-page: 42 year: 2008 ident: 000322626500009.4 publication-title: Angew. Chem. Int. Ed. – volume: 74 start-page: 4834 year: 2009 ident: WOS:000267432700022 article-title: Site-Isolation and Recycling of PdCl2 using PDMS Thimbles publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo900570y – volume: 120 start-page: 4716 year: 2008 ident: 000322626500009.28 publication-title: Angew. Chem. – volume: 2011 start-page: 3347 year: 2011 ident: WOS:000291583700010 article-title: Chiral Primary Amine Catalyzed Asymmetric Direct Cross-Aldol Reaction of Acetaldehyde publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ejoc.201100267 – volume: 44 start-page: 248 year: 2011 ident: 000322626500009.39 publication-title: Acc. Chem. Res. – volume: 120 start-page: 4710 year: 2008 ident: 000322626500009.17 publication-title: Angew. Chem. – volume: 113 start-page: 76 year: 2001 ident: 000322626500009.36 publication-title: Angew. Chem. |
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| Title | Paraldehyde as an Acetaldehyde Precursor in Asymmetric Michael Reactions Promoted by Site-Isolated Incompatible Catalysts |
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