Singh, Buddh and Gupta, Pankaj and Chaubey, Asha and Parshad, Rajinder and Sharma, Shiromani and Taneja, Subhash C. (2008) Enantiomerically pure α-methoxyaryl acetaldehydes as versatile precursors: a facile chemo-enzymatic methodology for their preparation. Tetrahedron: Asymmetry, 19 (22). pp. 2579-2588. ISSN 09574166

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Abstract

A facile and efficient synthesis of optically active a-methoxyaryl acetic acids (up to 95% ee), a-methoxyaryl ethanols (up to 93% ee) and a-methoxyaryl acetonitriles (up to 93% ee) was achieved via Arthrobacter sp. lipase-catalyzed kinetic resolution of masked aldehydes as the key synthons, that is, a-hydroxyaryl acetaldehyde acetals.

Item Type:	Article
Subjects:	Chemical Sciences
Divisions:	UNSPECIFIED
Depositing User:	Mr. Amit Nargotra
Date Deposited:	28 Dec 2011 08:34
Last Modified:	28 Dec 2011 08:34
URI:	http://iiim.csircentral.net/id/eprint/248

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