Usage and development of optically active cyclic 1,2-diols

Hiroshi Suemune, Mariko Aso

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Optically active diols are one of the useful groups of compounds for asymmetric reaction as a chiral auxiliary or ligand. Among them, cyclic 1,2-diols are characteristic of the restricted conformation. In this review, we wish to report the use of these compounds for the development of asymmetric reactions such as ring transformations based on intramolecular and intermolecular aldol reactions, and carba-spirocyclization, in which cyclic 1,2-diols are added as a chiral source in combination with a Lewis acid. In addition, the synthesis of optically active cyclic diene comp pounds starting from cyclic 1,2-diols is also discussed.

Original languageEnglish
Pages (from-to)807-814
Number of pages8
JournalYuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
Volume63
Issue number8
DOIs
Publication statusPublished - Jan 1 2005

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Lewis Acids
Conformations
Ligands
3-hydroxybutanal

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Usage and development of optically active cyclic 1,2-diols. / Suemune, Hiroshi; Aso, Mariko.

In: Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, Vol. 63, No. 8, 01.01.2005, p. 807-814.

Research output: Contribution to journalArticle

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