摘要
A C1-C7 fragment of the HIV-active Didemnaketal A analogue was synthesized from (R)-pulegone through 12 steps. Two new chiral centers, C3, C4 were successfully constructed by the steric induction in this approach and the aldehyde was selectively reduced.
A C1-C7 fragment of the HIV-active Didemnaketal A analogue was synthesized from (R)-pulegone through 12 steps. Two new chiral centers, C3, C4 were successfully constructed by the steric induction in this approach and the aldehyde was selectively reduced.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
2000年第5期729-730,共2页
Chemical Journal of Chinese Universities
基金
国家教委博士点专项基金!(批准号:96073006)
教育部跨世纪人才基金
国家杰出青年基金!(批准号:29925205)
