Synthesis and stereochemical behavior of (E)-cyclononene derivatives

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3 Citations (Scopus)

Abstract

A versatile synthetic approach to planar chiral molecules from (E)-5-cyclononen-1-one (1) has been developed; these molecules have multifunctionalities with (E)-cyclononene skeleton. The newly synthesized keto-ester 3 having central chirality shows labile planar chirality. In contrast, enol derivative 4 and enyne 5 show robust planar chirality.

Original languageEnglish
Pages (from-to)591-593
Number of pages3
JournalChemistry Letters
Volume40
Issue number6
DOIs
Publication statusPublished - May 27 2011

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Chirality
Derivatives
Molecules
Esters

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

Synthesis and stereochemical behavior of (E)-cyclononene derivatives. / Tomooka, Katsuhiko; Inoue, Hiroko; Igawa, Kazunobu.

In: Chemistry Letters, Vol. 40, No. 6, 27.05.2011, p. 591-593.

Research output: Contribution to journalArticle

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