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 journalArticle

27 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 languageEnglish
Pages (from-to)963-965
Number of pages3
JournalOrganic Letters
Volume8
Issue number5
DOIs
Publication statusPublished - Mar 2 2006
Externally publishedYes

Fingerprint

Amides
amides
Amines
amines
Derivatives
Chirality
synthesis
chirality
Nitrogen
nitrogen

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Planar chiral cyclic amine and its derivatives : Synthesis and stereochemical behavior. / Tomooka, Katsuhiko; Suzuki, Masaki; Shimada, Maki; Yanagitsuru, Syun Ichi; Uehara, Kazuhiro.

In: Organic Letters, Vol. 8, No. 5, 02.03.2006, p. 963-965.

Research output: Contribution to journalArticle

Tomooka, Katsuhiko ; Suzuki, Masaki ; Shimada, Maki ; Yanagitsuru, Syun Ichi ; Uehara, Kazuhiro. / Planar chiral cyclic amine and its derivatives : Synthesis and stereochemical behavior. In: Organic Letters. 2006 ; Vol. 8, No. 5. pp. 963-965.
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