Abstract
An application of readily available hydrazides in the Petasis 3-component coupling reaction is presented. An investigation of the substrate scope was performed to establish a general, synthetically useful protocol for the formation of hydrazido alcohols, which were selectively converted to oxazolidinone and oxadiazolone ring systems through triphosgene-mediated cyclization reactions.
Originalsprog | Engelsk |
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Tidsskrift | Organic Letters |
Vol/bind | 14 |
Udgave nummer | 2 |
Sider (fra-til) | 640-643 |
Antal sider | 4 |
ISSN | 1523-7060 |
DOI | |
Status | Udgivet - 20 jan. 2012 |