Chiral acetals in organic synthesis: regioselective synthesis of 2-and 3-hydroxy acetals from 2,3-olefinic acetals. Reinvestigation and further applications

Vankar, Yashwant D. ; Venkatram Reddy, M. ; Chaudhuri, Narayan C. (1994) Chiral acetals in organic synthesis: regioselective synthesis of 2-and 3-hydroxy acetals from 2,3-olefinic acetals. Reinvestigation and further applications Tetrahedron, 50 (37). pp. 11057-11078. ISSN 0040-4020

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/S0040-4020(01)85714-8

Abstract

Achiral as well as chiral 2,3-olefinic acetals are converted into 2- and 3- hydroxy acetals via LAH reduction of the corresponding epoxides and via bromohydrins followed by TBTH reductions respectively. Synthesis of 1,3-diones is described. Compounds from chiral systems are further utilized for asymmetric synthesis.

Item Type:Article
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ID Code:58197
Deposited On:31 Aug 2011 06:35
Last Modified:31 Aug 2011 06:35

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