Issue 24, 1987

Hydroboration of prochiral olefins with chiral Lewis base–borane complexes: relationship to the mechanism of hydroboration

Abstract

Alcohols with up to 19% enantiomeric excess were obtained on hydroboration/oxidation of representative prochiral olefins using N-isobornyl-N-methylaniline–borane or N-benzyl-N-isopropyl-α-methylbenzylamine–borane indicating that the Lewis base is present in the hydroboration transition state.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 1857-1859

Hydroboration of prochiral olefins with chiral Lewis base–borane complexes: relationship to the mechanism of hydroboration

C. Narayana and M. Periasamy, J. Chem. Soc., Chem. Commun., 1987, 1857 DOI: 10.1039/C39870001857

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements