Diastereoselective synthesis of fused oxazolidines and highly substituted 1H-pyrrolo 2,1-c]1,4] oxazines via C-H functionalization

Pavan Kumar, C. S. and Harsha, K. B. and Mantelingu, K. and Rangappa, K. S. (2015) Diastereoselective synthesis of fused oxazolidines and highly substituted 1H-pyrrolo 2,1-c]1,4] oxazines via C-H functionalization. RSC ADVANCES, 5 (76). pp. 61664-61670. ISSN 2046-2069

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Official URL: http://doi.org/10.1039/c5ra10030e

Abstract

The first one pot protocol for the diastereoselective synthesis of oxazolo2,3-c]isoquinoline was achieved by a metal-free, benzoic acid catalyzed reaction of 1,2,3,4-tetrahydroisoquinoline or trypoline with aldehydes under mild conditions via C-H, C-O bond functionalization. A new approach for the synthesis of highly substituted 1H-pyrrolo2,1-c]1,4]oxazine was carried out.

Item Type: Article
Subjects: C Chemical Science > Chemistry
Divisions: Department of > Chemistry
Depositing User: Shrirekha N
Date Deposited: 18 Jun 2019 06:18
Last Modified: 24 Dec 2019 09:23
URI: http://eprints.uni-mysore.ac.in/id/eprint/3252

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