Preparation of optically active (R)- and (S)-allene-1,3-dicarboxylates and their asymmetric cycloaddition reactions with cyclopentadiene

Mariko Aso; Izumi Ikeda; Tsuyoshi Kawabe; Motoo Shiro; Ken Kanematsu

doi:10.1016/0040-4039(92)89032-8

Preparation of optically active (R)- and (S)-allene-1,3-dicarboxylates and their asymmetric cycloaddition reactions with cyclopentadiene

Mariko Aso, Izumi Ikeda, Tsuyoshi Kawabe, Motoo Shiro, Ken Kanematsu

Chemo-Pharmaceutical Sciences

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

25 Citations (Scopus)

Abstract

Optically active (R)- and (S)- allene-1,3-dicarboxylates were prepared, and their asymmetric Diels-Alder reactions with cyclopentadiene in the presence of Lewis acid proceeded to afford the endo-adducts in high yields.

Original language	English
Pages (from-to)	5787-5790
Number of pages	4
Journal	Tetrahedron Letters
Volume	33
Issue number	39
DOIs	https://doi.org/10.1016/0040-4039(92)89032-8
Publication status	Published - Sept 22 1992

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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title = "Preparation of optically active (R)- and (S)-allene-1,3-dicarboxylates and their asymmetric cycloaddition reactions with cyclopentadiene",

abstract = "Optically active (R)- and (S)- allene-1,3-dicarboxylates were prepared, and their asymmetric Diels-Alder reactions with cyclopentadiene in the presence of Lewis acid proceeded to afford the endo-adducts in high yields.",

author = "Mariko Aso and Izumi Ikeda and Tsuyoshi Kawabe and Motoo Shiro and Ken Kanematsu",

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AU - Aso, Mariko

AU - Ikeda, Izumi

AU - Kawabe, Tsuyoshi

AU - Shiro, Motoo

AU - Kanematsu, Ken

PY - 1992/9/22

Y1 - 1992/9/22

N2 - Optically active (R)- and (S)- allene-1,3-dicarboxylates were prepared, and their asymmetric Diels-Alder reactions with cyclopentadiene in the presence of Lewis acid proceeded to afford the endo-adducts in high yields.

AB - Optically active (R)- and (S)- allene-1,3-dicarboxylates were prepared, and their asymmetric Diels-Alder reactions with cyclopentadiene in the presence of Lewis acid proceeded to afford the endo-adducts in high yields.

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JO - Tetrahedron Letters

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ER -

Preparation of optically active (R)- and (S)-allene-1,3-dicarboxylates and their asymmetric cycloaddition reactions with cyclopentadiene

Abstract

All Science Journal Classification (ASJC) codes

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