Synthesis of 9,11-Ethano-13,15-isoxazolinoprostanoids, PGH Analogs
摘要:
The 1,3-dipolar addition to terminal alkenes of nitrile oxides generated from nitromethylene derivatives of bicycloheptane provided 9,11-ethano-13,15-isoxazolinoprostanoids with alkyl, phenyl, or additional heterocyclic fragment in the omega-chain.
OXENRIDER, B. C.;ROGIC, M. M., J. ORG. CHEM., 1982, 47, N 13, 2629-2633
作者:OXENRIDER, B. C.、ROGIC, M. M.
DOI:——
日期:——
US4393215A
申请人:——
公开号:US4393215A
公开(公告)日:1983-07-12
Synthesis of 9,11-Ethano-13,15-isoxazolinoprostanoids, PGH Analogs
作者:N. F. Bondar'、L. P. Isaenya、R. V. Skupskaya、F. A. Lakhvich
DOI:10.1023/b:rujo.0000010175.39145.9a
日期:2003.8
The 1,3-dipolar addition to terminal alkenes of nitrile oxides generated from nitromethylene derivatives of bicycloheptane provided 9,11-ethano-13,15-isoxazolinoprostanoids with alkyl, phenyl, or additional heterocyclic fragment in the omega-chain.
Reactions of 2,2-dialkoxy ketone oximes with chlorine and bromine. Halogenation vs. Beckmann fragmentation