Structure and asymmetric diels-alder reactions of optically active allene-1,3-dicarboxylates

Izumi Ikeda, Kazuhiko Honda, Eiji Osawa, Motoo Shiro, Mariko Aso, Ken Kanematsu

Research output: Contribution to journalArticle

37 Citations (Scopus)

Abstract

Optically active allene-1,3-dicarboxylates (1a and 2a), which contain the axial asymmetry of the allene moiety, were prepared. The Diels-Alder reaction of 1a and 2a with cyclopentadiene afforded the 1:1 (1a or 2a to cyclopentadiene) endo adducts 3a and 4a through the combination of the sterically favorable approach of the diene and the dienophile owing to the axial asymmetry of the allene moiety and the effective secondary orbital interaction. The absolute configurations of 3a and 4a were determined by chemical transformation and X-ray analysis. The absolute configuration of the axial asymmetry of 1a was also determined to be R by X-ray analysis.

Original languageEnglish
Pages (from-to)2031-2037
Number of pages7
JournalJournal of Organic Chemistry
Volume61
Issue number6
DOIs
Publication statusPublished - Dec 1 1996

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Cyclopentanes
X ray analysis
propadiene

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

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Structure and asymmetric diels-alder reactions of optically active allene-1,3-dicarboxylates. / Ikeda, Izumi; Honda, Kazuhiko; Osawa, Eiji; Shiro, Motoo; Aso, Mariko; Kanematsu, Ken.

In: Journal of Organic Chemistry, Vol. 61, No. 6, 01.12.1996, p. 2031-2037.

Research output: Contribution to journalArticle

Ikeda, Izumi ; Honda, Kazuhiko ; Osawa, Eiji ; Shiro, Motoo ; Aso, Mariko ; Kanematsu, Ken. / Structure and asymmetric diels-alder reactions of optically active allene-1,3-dicarboxylates. In: Journal of Organic Chemistry. 1996 ; Vol. 61, No. 6. pp. 2031-2037.
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