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.
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.