Highly enantioselective catalytic isopropenylation of aldehydes using diisopropenylzinc

Takanori Shibata, Kazuhiro Nakatsui, Kenso Soai

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

Diisopropenylzinc adds highly enantioselectively to various aldehydes in the presence of a catalytic amount of chiral amino alcohols to give enantiomerically enriched allyl alkanols with up to 92% e.e.

Original languageEnglish
Pages (from-to)33-36
Number of pages4
JournalInorganica Chimica Acta
Volume296
Issue number1
Publication statusPublished - 1999 Dec 15
Externally publishedYes

Fingerprint

Amino alcohols
Amino Alcohols
Aldehydes
aldehydes
alcohols

Keywords

  • Alkenyl complexes
  • Alkylation
  • Enantioselective catalysis
  • Zinc complexes

ASJC Scopus subject areas

  • Biochemistry
  • Inorganic Chemistry
  • Physical and Theoretical Chemistry
  • Materials Chemistry

Cite this

Highly enantioselective catalytic isopropenylation of aldehydes using diisopropenylzinc. / Shibata, Takanori; Nakatsui, Kazuhiro; Soai, Kenso.

In: Inorganica Chimica Acta, Vol. 296, No. 1, 15.12.1999, p. 33-36.

Research output: Contribution to journalArticle

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