Issue 5, 1987

Microbial resolution and asymmetric reduction related to optically active 1,3-diphenylpropane-1,3-diol

Abstract

An efficient microbial resolution of 1,3-diphenylpropane-1,3-diol (4) has been achieved by exposing the corresponding diacetate to Trichoderma viride; a reductive cleavage of chiral acetals (6) derived from (4) with hydride reagent (Br2AlH, Cl2AlH) affords optically active alcohols (8) of high enantiomeric purities.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 334-335

Microbial resolution and asymmetric reduction related to optically active 1,3-diphenylpropane-1,3-diol

K. Yamamoto, H. Ando and H. Chikamatsu, J. Chem. Soc., Chem. Commun., 1987, 334 DOI: 10.1039/C39870000334

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