Synthesis of the C1–C20 and C15–C27 Segments of Aplyronine A
摘要:
The synthesis of C1-C20 and C15-C27 segments of Aplyronine A is described. Oxidative cleavage of cyclic vinyl sulfones has been used to prepare key fragments of Aplyronine A. Key precursors are united by Horner-Wadsworth-Emmons and Julia-Kociensky olefination for the respective elaboration of the C1-C20 and C15-C27 segments.
[EN] LARGE-SCALE DIASTEREOSELECTIVE SYNTHESES OF CYCLOHEPTADIENYLSULFONES AND STEREOTETRADS [FR] SYNTHESES DIASTEREOSELECTIVES A GRANDE ECHELLE DE CYCLOHEPTADIENYLSULFONES ET DE STEREOTETRADES
[EN] LARGE-SCALE DIASTEREOSELECTIVE SYNTHESES OF CYCLOHEPTADIENYLSULFONES AND STEREOTETRADS<br/>[FR] SYNTHESES DIASTEREOSELECTIVES A GRANDE ECHELLE DE CYCLOHEPTADIENYLSULFONES ET DE STEREOTETRADES
申请人:PURDUE RESEARCH FOUNDATION
公开号:WO2016057606A1
公开(公告)日:2016-04-14
The invention relates to processes for large-scale diastereoselective syntheses of cycloheptadienylsulfone and stereo tetrads, key intermediates for the preparation of Aplyronine A.
Synthesis of the C1–C20 and C15–C27 Segments of Aplyronine A
作者:Wan Pyo Hong、Mohammad N. Noshi、Ahmad El-Awa、Philip L. Fuchs
DOI:10.1021/ol2024746
日期:2011.12.16
The synthesis of C1-C20 and C15-C27 segments of Aplyronine A is described. Oxidative cleavage of cyclic vinyl sulfones has been used to prepare key fragments of Aplyronine A. Key precursors are united by Horner-Wadsworth-Emmons and Julia-Kociensky olefination for the respective elaboration of the C1-C20 and C15-C27 segments.