Total Synthesis and Absolute Configuration of (-)-Sedacryptine

Eiji Akiyama; Masahiro Hirama

doi:10.1055/s-1996-5335

Total Synthesis and Absolute Configuration of (-)-Sedacryptine

Eiji Akiyama, Masahiro Hirama

Materials Design Division

Research output: Contribution to journal › Article › peer-review

19 Citations (Scopus)

Abstract

Enantioselective synthesis of (-)-sedacryptine, a piperidine alkaloid, has been achieved via the double intramolecular conjugate additions of carbamate group and its absolute configuration was determined.

Original language	English
Pages (from-to)	100-102
Number of pages	3
Journal	Synlett
Volume	1996
Issue number	1
DOIs	https://doi.org/10.1055/s-1996-5335
Publication status	Published - 1996 Jan 1

ASJC Scopus subject areas

Organic Chemistry

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abstract = "Enantioselective synthesis of (-)-sedacryptine, a piperidine alkaloid, has been achieved via the double intramolecular conjugate additions of carbamate group and its absolute configuration was determined.",

author = "Eiji Akiyama and Masahiro Hirama",

year = "1996",

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Total Synthesis and Absolute Configuration of (-)-Sedacryptine

Abstract

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