Organocatalytic Enantioselective Approach to Spirocyclic Δβ,γ-Butenolides
Brak miniatury
Data
2014
Tytuł czasopisma
ISSN czasopisma
Tytuł tomu
Wydawca
Abstrakt
A novel method for the preparation of the spirocyclic Δβ,γ-butenolides is presented. The developed strategy is based on a trienamine-mediated [4+2]-cycloaddition between (E)-3-alkylidene- 5-arylfuran-2(3H)-ones and 2,4-dienals. Target products containing three contiguous centres including one quaternary are efficiently formed in a highly enantiomerically enriched form in the presence of the silyl-protected diphenylprolinol aminocatalyst.
Opis
Słowa kluczowe
asymmetric synthesis, aminocatalysis, trienamines, Δβ,γ-butenolides, quaternary stereogenic center
Cytowanie
Synlett, Vol. 25(20), pages 2957-2961