First enantioselective synthesis of (+)-quinolizidine 207I: Determination of the absolute stereochemistry

Naoki Toyooka; Hideo Nemoto

doi:10.1016/S0040-4039(02)02540-6

First enantioselective synthesis of (+)-quinolizidine 207I: Determination of the absolute stereochemistry

Naoki Toyooka^*, Hideo Nemoto

^*Corresponding author for this work

Life Sciences and Bioengineering

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

22 Scopus citations

Abstract

First enantioselective synthesis of quinolizidine 207I has been achieved and the absolute stereochemistry of natural quinolizidine 207I was determined to be 1S,4S,10S by the present chiral synthesis using GC analysis with β-dextrin chiral column on co-injection with racemate.

Original language	English
Pages (from-to)	569-570
Number of pages	2
Journal	Tetrahedron Letters
Volume	44
Issue number	3
DOIs	https://doi.org/10.1016/S0040-4039(02)02540-6
State	Published - 2003/01/13

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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title = "First enantioselective synthesis of (+)-quinolizidine 207I: Determination of the absolute stereochemistry",

abstract = "First enantioselective synthesis of quinolizidine 207I has been achieved and the absolute stereochemistry of natural quinolizidine 207I was determined to be 1S,4S,10S by the present chiral synthesis using GC analysis with β-dextrin chiral column on co-injection with racemate.",

author = "Naoki Toyooka and Hideo Nemoto",

year = "2003",

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doi = "10.1016/S0040-4039(02)02540-6",

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T1 - First enantioselective synthesis of (+)-quinolizidine 207I

T2 - Determination of the absolute stereochemistry

AU - Toyooka, Naoki

AU - Nemoto, Hideo

PY - 2003/1/13

Y1 - 2003/1/13

N2 - First enantioselective synthesis of quinolizidine 207I has been achieved and the absolute stereochemistry of natural quinolizidine 207I was determined to be 1S,4S,10S by the present chiral synthesis using GC analysis with β-dextrin chiral column on co-injection with racemate.

AB - First enantioselective synthesis of quinolizidine 207I has been achieved and the absolute stereochemistry of natural quinolizidine 207I was determined to be 1S,4S,10S by the present chiral synthesis using GC analysis with β-dextrin chiral column on co-injection with racemate.

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U2 - 10.1016/S0040-4039(02)02540-6

DO - 10.1016/S0040-4039(02)02540-6

M3 - 学術論文

AN - SCOPUS:0037433986

SN - 0040-4039

VL - 44

SP - 569

EP - 570

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 3

ER -

First enantioselective synthesis of (+)-quinolizidine 207I: Determination of the absolute stereochemistry

Abstract

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