(3+3) Annulation of acetoxy allenoates with enolisable carbonyl substrates leading to fused pyrans

Lewis base dependent (3 + 3) annulation of delta-acetoxy allenoates with benzofuranone, pyrazolone, and Boc-protected oxindole is reported. In the presence of catalytic DBU, oxindole, benzofuranone, and pyrazolone undergo (3 + 3) annulation with delta-acetoxy allenoates via 6-exo-dig cyclisation at...

Celý popis

Uložené v:
Podrobná bibliografia
Vydané v:Organic & biomolecular chemistry Ročník 21; číslo 24; s. 5021 - 5032
Hlavní autori: Chauhan, Sachin, Debnath, Shubham, Swamy, K. C. Kumara
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: CAMBRIDGE Royal Soc Chemistry 21.06.2023
Predmet:
Chemistry
Chemistry, Organic
Physical Sciences
Science & Technology
ISSN:1477-0520, 1477-0539, 1477-0539
On-line prístup:Zistit podrobnosti o prístupe
Tagy: Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
Popis
Shrnutí:Lewis base dependent (3 + 3) annulation of delta-acetoxy allenoates with benzofuranone, pyrazolone, and Boc-protected oxindole is reported. In the presence of catalytic DBU, oxindole, benzofuranone, and pyrazolone undergo (3 + 3) annulation with delta-acetoxy allenoates via 6-exo-dig cyclisation at room temperature (25 degrees C) to afford fused pyran scaffolds. On the other hand, by employing catalytic DMAP, the reaction between N-Boc-oxindole and delta-acetoxy allenoates goes through 6-endo-dig cyclisation, leading to distinct dihydropyrans that contain an exocyclic double bond; similar products were also obtained by using benzofuranone and pyrazolone.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1477-0520
1477-0539
1477-0539
DOI:10.1039/d3ob00597f