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Details

Autor(en) / Beteiligte
Titel
Stabilized Sulfur Ylide Mediated Cyclopropanations and Formal [4+1] Cycloadditions of 3-Acyl-2H-chromenones and Their Imines
Ist Teil von
  • European journal of organic chemistry, 2016-10, Vol.2016 (28), p.4778-4781
Ort / Verlag
Weinheim: Blackwell Publishing Ltd
Erscheinungsjahr
2016
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Stabilized sulfur ylide mediated cyclopropanation and formal [4+1] cycloaddition of 3‐acyl‐2H‐chromenones and their imines were explored. The transformations could be performed under mild conditions and were shown to have wide substrate scopes and significant functional‐group tolerance; furthermore, the reactions proceeded with excellent regioselectivity. Thus, they are powerful methods for the one‐pot synthesis of highly functionalized cyclopropane‐ and dihydropyrrole‐fused chromen‐2‐one derivatives. Stabilized sulfur ylide mediated cyclopropanation and formal [4+1] cycloaddition of 3‐acyl‐2H‐chromenones and their imines are developed. These transformations have wide substrate scopes and proceed with excellent regioselectivity; thus, they are powerful methods for the one‐pot synthesis of highly functionalized cyclopropane‐ and dihydropyrrole‐fused chromen‐2‐one derivatives.
Sprache
Englisch
Identifikatoren
ISSN: 1434-193X
eISSN: 1099-0690
DOI: 10.1002/ejoc.201600759
Titel-ID: cdi_proquest_journals_1826189023

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