Regioselective synthesis of 3-(1H-indol-3-yl)-5-(1H-indole-3-carbonyl)-4-hydroxyfuroic acids: route to hydroxyfuroic acid-based insulin receptor activators
Author:
Publisher
Wiley
Subject
Drug Discovery
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ddr.20391/fullpdf
Reference19 articles.
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2. Chen SS Zhang B Li X. 2003
3. Regioselective synthesis of 3-aryl-5-(1H-indole-3-carbonyl)-4-hydroxyfuroic acids as potential insulin receptor activators;Chou;Tetrahedron Lett,2006
4. Mice lacking dipeptidyl peptidase IV are protected against obesity and insulin resistance;Conarello;Proc Natl Acad Sci USA,2003
5. The discovery of type 1 diabetes;Gale;Diabetes,2001
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1. Versatile access to nitrogen-rich π-extended indolocarbazoles via a Pictet–Spengler approach;Organic Chemistry Frontiers;2023
2. Brønsted acidic ionic liquid-promoted direct C3-acylation of N-unsubstituted indoles with acid anhydrides under microwave irradiation;RSC Advances;2017
3. Domino Cyclodimerization of Indole-Derived Donor-Acceptor Cyclopropanes: One-Step Construction of the Pentaleno[1,6-a,b]indole Skeleton;Chemistry - A European Journal;2011-09-12
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