Chiral synthesis of (+)-eburnamine, (–)-eburnamenine, and (–)-eburnamonine

Chiral synthesis of (+)-eburnamine, (–)-eburnamenine, and (–)-eburnamonine
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(+)-依布那明、(–)-依布那胺和 (–)-依布那莫宁的手性合成

DOI:
10.1039/p19850000305
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发表时间:
1985
期刊:
Journal of The Chemical Society-perkin Transactions 1
影响因子:
--
通讯作者:
K. Ogasawara*
K. Ogasawara*
中科院分区:
--
文献类型:
--
作者:
S. Takano*;M. Yonaga;M. Morimoto;K. Ogasawara*

文献摘要

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容易由l-谷氨酸或d -甘露醇制备的(S)-三烷基内酯(6)通过二硫烷内酯(15)立体选择性地转化为(+)-eburnamine(3)、(-)-eburnamine(4)和(-)-eburnamonine(2)。
The (S)-trityl-lactone (6), easily prepared from L-glutamic acid or D-mannitol, has been stereo-selectively converted into (+)-eburnamine (3), (–)-eburnamenine (4), and (–)-eburnamonine (2), via the dithiane-lactone (15).