| Literature DB >> 28829915 |
Eslam B Elkaeed1,2, Jing An1, André M Beauchemin1.
Abstract
Nitrogen-substituted isocyanates (N-isocyanates) are rare amphoteric reagents with high, but underdeveloped synthetic potential. Herein, we study the formation of indazolones by Friedel-Crafts cyclization of N-isocyanates using blocked (masked) N-isocyanate precursors: the effect of the masking group and the reaction scope have been delineated. Substrate synthesis has also been improved using a reported copper-catalyzed coupling of arylbismuth(V) reagents that is compatible with the hemilabile OPh blocking group.Entities:
Year: 2017 PMID: 28829915 DOI: 10.1021/acs.joc.7b01607
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354