Issue 3, 2017

Unusual reversal of enantioselectivity in the asymmetric autocatalysis of pyrimidyl alkanol triggered by chiral aromatic alkanols and amines

Abstract

Temperature dependent inversion of enantioselectivity in asymmetric catalysis is an interesting and somewhat unusual phenomenon. We have observed temperature dependent inversion of enantioselectivity in the asymmetric autocatalysis reaction when triggered by a wide scope of enantioenriched alcohols and amines. The addition reaction of diisopropylzinc to pyrimidine-5-carbaldehyde in the presence of enantiopure alcohols or amines affords the pyrimidyl alkanol product at 0 °C with high ee. However, lowering the reaction temperature to −44 °C affords the opposite enantioselectivity.

Graphical abstract: Unusual reversal of enantioselectivity in the asymmetric autocatalysis of pyrimidyl alkanol triggered by chiral aromatic alkanols and amines

Article information

Article type
Communication
Submitted
06 Nov 2016
Accepted
02 Dec 2016
First published
02 Dec 2016
This article is Open Access
Creative Commons BY-NC license

Org. Biomol. Chem., 2017,15, 555-558

Unusual reversal of enantioselectivity in the asymmetric autocatalysis of pyrimidyl alkanol triggered by chiral aromatic alkanols and amines

A. Matusmoto, S. Fujiwara, Y. Hiyoshi, K. Zawatzky, A. A. Makarov, C. J. Welch and K. Soai, Org. Biomol. Chem., 2017, 15, 555 DOI: 10.1039/C6OB02415G

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