Rh-catalyzed enantioselective hydrogenation of vinyl boronates for the construction of secondary boronic esters

Moran, Wesley J. and Morken, James P. (2006) Rh-catalyzed enantioselective hydrogenation of vinyl boronates for the construction of secondary boronic esters. Organic Letters, 8 (11). pp. 2413-2419. ISSN 15237060

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Abstract

Rh-catalyzed hydrogenation of prochiral vinyl boronates occurs in an enantioselective fashion in the presence of the chiral ligand Walphos 1. This transformation provides access to chiral secondary organoboronates that are not available from alkene hydroboration reactions. The chiral reaction products should be useful in organic synthesis, and preliminary experiments suggest that they may participate in one-pot amination and homologation reactions.

Item Type:	Article
Subjects:	Q Science > Q Science (General) Q Science > QD Chemistry
Schools:	School of Applied Sciences
Related URLs:	Author
Depositing User:	Sara Taylor
Date Deposited:	30 Jun 2008 14:33
Last Modified:	28 Aug 2021 10:39
URI:	http://eprints.hud.ac.uk/id/eprint/949

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