Planar chiral cyclic amine and its derivatives: Synthesis and stereochemical behavior

Katsuhiko Tomooka; Masaki Suzuki; Maki Shimada; Syun Ichi Yanagitsuru; Kazuhiro Uehara

doi:10.1021/ol053141k

Planar chiral cyclic amine and its derivatives: Synthesis and stereochemical behavior

Katsuhiko Tomooka, Masaki Suzuki, Maki Shimada, Syun Ichi Yanagitsuru, Kazuhiro Uehara

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

33 Citations (Scopus)

Abstract

Nine-membered diallylic cyclic amines and amides have remarkably stable planar chirality. The transformation of enantiomerically enriched amides provides optically active nitrogen heterocycles containing stereogenic centers in a stereospecific fashion.

Original language	English
Pages (from-to)	963-965
Number of pages	3
Journal	Organic letters
Volume	8
Issue number	5
DOIs	https://doi.org/10.1021/ol053141k
Publication status	Published - Mar 2 2006
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol053141k

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title = "Planar chiral cyclic amine and its derivatives: Synthesis and stereochemical behavior",

abstract = "Nine-membered diallylic cyclic amines and amides have remarkably stable planar chirality. The transformation of enantiomerically enriched amides provides optically active nitrogen heterocycles containing stereogenic centers in a stereospecific fashion.",

author = "Katsuhiko Tomooka and Masaki Suzuki and Maki Shimada and Yanagitsuru, {Syun Ichi} and Kazuhiro Uehara",

year = "2006",

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doi = "10.1021/ol053141k",

language = "English",

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journal = "Organic Letters",

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T1 - Planar chiral cyclic amine and its derivatives

T2 - Synthesis and stereochemical behavior

AU - Tomooka, Katsuhiko

AU - Suzuki, Masaki

AU - Shimada, Maki

AU - Yanagitsuru, Syun Ichi

AU - Uehara, Kazuhiro

PY - 2006/3/2

Y1 - 2006/3/2

N2 - Nine-membered diallylic cyclic amines and amides have remarkably stable planar chirality. The transformation of enantiomerically enriched amides provides optically active nitrogen heterocycles containing stereogenic centers in a stereospecific fashion.

AB - Nine-membered diallylic cyclic amines and amides have remarkably stable planar chirality. The transformation of enantiomerically enriched amides provides optically active nitrogen heterocycles containing stereogenic centers in a stereospecific fashion.

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U2 - 10.1021/ol053141k

DO - 10.1021/ol053141k

M3 - Article

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VL - 8

SP - 963

EP - 965

JO - Organic Letters

JF - Organic Letters

IS - 5

ER -

Planar chiral cyclic amine and its derivatives: Synthesis and stereochemical behavior

Abstract

All Science Journal Classification (ASJC) codes

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