Montmorillonite clay catalyzed synthesis of enantiomerically pure 1,2,3,4-tetrahydroquinolines

Yadav, J. S. ; Reddy, B. V. S. ; Meraj, Syeda ; Vishnumurthy, P. ; Narsimulu, K. ; Kunwar, A. C. (2006) Montmorillonite clay catalyzed synthesis of enantiomerically pure 1,2,3,4-tetrahydroquinolines Synthesis, 2006 (17). pp. 2923-2926. ISSN 0039-7881

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Official URL: https://www.thieme-connect.com/ejournals/abstract/...

Related URL: http://dx.doi.org/10.1055/s-2006-942528

Abstract

Arylamines undergo smooth cyclization with 2-deoxy-D-ribose on the surface of montmorillonite KSF clay under mild conditions to afford the corresponding sugar-derived chiral tetrahydroquinolines in high yields with moderate diastereoselectivity. The assignment of the stereochemistry of the product was achieved by various NMR studies.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:2-deoxy Sugars; Solid Acid; Arylamines; Tetrahydroquinolines
ID Code:63219
Deposited On:28 Sep 2011 03:26
Last Modified:28 Sep 2011 03:26

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