Chiral synthesis of optically active S(+)-2,6,7,7a-tetrahydro-1β-hydroxy-4-formyl-7aβ-methylindene

Banerjee, D. K. ; Kasturi, T. R. ; Sarkar, A. (1983) Chiral synthesis of optically active S(+)-2,6,7,7a-tetrahydro-1β-hydroxy-4-formyl-7aβ-methylindene Proceedings of the Indian Academy of Sciences - Chemical Sciences, 92 (2). pp. 181-187. ISSN 0253-4134

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Official URL: http://www.ias.ac.in/j_archive/chemsci/92/2/181-18...

Related URL: http://dx.doi.org/10.1007/BF02840729

Abstract

The chiral aldol cylization of the prochiral triketone 3 using l-valine afforded the optically active compound 4 in high chemical and optical yield. The configuration and optical purity of (+)4 was determined by ORD, chemical resolution and NMR chiral lsr studies. The title compound (+)7 was prepared from (+)4 following our earlier reported procedure.

Item Type:Article
Source:Copyright of this article belongs to Indian Academy of Sciences.
Keywords:Chiral Synthesis; Chemical Resolution; Optical Rotatory Dispersion; Chiral NMR Shift Reagent
ID Code:26381
Deposited On:06 Dec 2010 12:38
Last Modified:17 May 2016 09:40

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