Highly Enantioselective Dihydroxylation of Trans-Disubstituted and Monosubstituted Olefins

Tohru Oishi, Masahiro Hirama

Research output: Contribution to journalLetter

92 Citations (Scopus)

Abstract

Extremely high levels of asymmetric induction have been achieved in osmium tetraoxide oxidation of trans-disubstituted and monosubstituted olefins by using chiral N,N'-dineohexyl-2,2'-bipyrrolidine ligand.

Original languageEnglish
Pages (from-to)5834-5835
Number of pages2
JournalJournal of Organic Chemistry
Volume54
Issue number25
DOIs
Publication statusPublished - Dec 1 1989
Externally publishedYes

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Osmium
Alkenes
Ligands
Oxidation

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Highly Enantioselective Dihydroxylation of Trans-Disubstituted and Monosubstituted Olefins. / Oishi, Tohru; Hirama, Masahiro.

In: Journal of Organic Chemistry, Vol. 54, No. 25, 01.12.1989, p. 5834-5835.

Research output: Contribution to journalLetter

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abstract = "Extremely high levels of asymmetric induction have been achieved in osmium tetraoxide oxidation of trans-disubstituted and monosubstituted olefins by using chiral N,N'-dineohexyl-2,2'-bipyrrolidine ligand.",
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N2 - Extremely high levels of asymmetric induction have been achieved in osmium tetraoxide oxidation of trans-disubstituted and monosubstituted olefins by using chiral N,N'-dineohexyl-2,2'-bipyrrolidine ligand.

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