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Synthesis 2003(16): 2525-2529
DOI: 10.1055/s-2003-42404
DOI: 10.1055/s-2003-42404
PAPER
© Georg Thieme Verlag Stuttgart · New YorkIsocyanatophosphoryl Dichloride as Reagent for Introduction of Carbamoyl Group into Molecules of π-Excessive Heterocycles and Enamines
Further Information
Received
4 July 2003
Publication Date:
29 September 2003 (online)
Publication History
Publication Date:
29 September 2003 (online)
Abstract
A study on the stepwise hydrolysis of hetarene- and cycloalkenecarboxamidophosphoryl dichlorides afforded the synthesis of hitherto unknown hetarene- and cycloalkene-carboxamidophosphoric acids as well as allowing the introduction of unsubstituted carbamoyl group in the molecules of pyrroles, indoles, indolizines, and some enamines.
Key words
carboxamides - isocyanatophosphoryl dichloride - carbonylamidophosphoric acids - indoles - pyrroles - indolizines - enamines
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