Stereoselective Synthesis of Substituted γ-Butyrolactones by the [3 + 2] Annulation of Allylic Silanes with Chlorosulfonyl Isocyanate: Enantioselective Total Synthesis of (+)-Blastmycinone
摘要:
[GRAPHICS]A stereoselective synthesis of gamma -butyrolactones by the [3 + 2] annulation of allylic silanes with N-chlorosulfonyl isocyanate (CSI) was developed. An enantioselective total synthesis of (+)-blastmycinone was accomplished using this annulation as the key step.
Stereoselective Synthesis of Substituted γ-Butyrolactones by the [3 + 2] Annulation of Allylic Silanes with Chlorosulfonyl Isocyanate: Enantioselective Total Synthesis of (+)-Blastmycinone
摘要:
[GRAPHICS]A stereoselective synthesis of gamma -butyrolactones by the [3 + 2] annulation of allylic silanes with N-chlorosulfonyl isocyanate (CSI) was developed. An enantioselective total synthesis of (+)-blastmycinone was accomplished using this annulation as the key step.
Stereoselective Synthesis of Substituted γ-Butyrolactones by the [3 + 2] Annulation of Allylic Silanes with Chlorosulfonyl Isocyanate: Enantioselective Total Synthesis of (+)-Blastmycinone
作者:Zhi-Hui Peng、K. A. Woerpel
DOI:10.1021/ol0069960
日期:2001.3.1
[GRAPHICS]A stereoselective synthesis of gamma -butyrolactones by the [3 + 2] annulation of allylic silanes with N-chlorosulfonyl isocyanate (CSI) was developed. An enantioselective total synthesis of (+)-blastmycinone was accomplished using this annulation as the key step.