Diastereoselective synthesis of fused oxazolidines and highly substituted 1H-pyrrolo [2, 1-c][1, 4] oxazines via C–H functionalization1. Issue 76 (19th August 2015)

• Record Type: Journal Article
• Authors: Pavan Kumar, Chottanahalli. S.; Harsha, Kachigere. B.; Mantelingu, Kempegowda; Rangappa, Kanchugarakoppal. S.
• Is Part Of: RSC advances. Volume 5:Issue 76(2015)
• Page Start: 61664
• Page End: 61670
• Publication Date: 2015-08-19
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c5ra10030e
• Languages: English
• ISSNs: 2046-2069

Abstract

<abstract abstract-type="toc"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <graphic position="anchor" id="ga" xlink:href="ark:/27927/pgj2b31c3w0" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" />The first one pot protocol for the diastereoselective synthesis of oxazolo[2, 3-<italic>c</italic>]isoquinoline was achieved by metal-free, benzoic acid catalyzed reactions under mild conditions <italic>via</italic> C–H, C–O bond functionalization.</p> </abstract>