J-STAGE トップ  >  資料トップ  > 書誌事項

有機合成化学協会誌
Vol. 71 (2013) No. 8 p. 844-845

記事言語:

http://doi.org/10.5059/yukigoseikyokaishi.71.844

Review de Debut

Optically active α,β-disubstituted β-lactone is a useful building blocks. Dyotropic rearrangement is the one of the featured transformation of β-lactone, which involves concurrent migration of two vicinal σ bonds to afford the multifunctionalized γ-butyrolactones. In 2012, two research groups were reported the natural product synthesis using the dyotropic rearrangement of β-lactone to make the 5,7 bicyclic ring systems and a highly constrained bridged spiro-γ-butyrolactone, respectively.

Copyright © 2013 社団法人 有機合成化学協会

記事ツール

この記事を共有