Isocyanatophosphoryl dichloride as reagent for introduction of carbamoyl group into molecules of π-excessive heterocycles and enamines

…, AA Chaikovskaya, AM Pinchuk, AA Tolmachev

Index: Smaliy, Radomir V.; Chaikovskaya, Aleksandra A.; Pinchuk, Aleksandr M.; Tolmachev, Andrei A. Synthesis, 2003 , # 16 p. 2525 - 2529

Full Text: HTML

Citation Number: 3

Abstract

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.

Iminoxyl radicals and stable products from the one-electron oxidation of 1-methylindole-3-carbaldehyde oximes

[Everett, Steven A.; Naylor, Matthew A.; Stratford, Michael R.L.; Patel, Kantilal B.; Ford, Eleonora; Mortensen, Alan; Ferguson, Amanda C.; Vojnovic, Borivoj; Wardman, Peter Journal of the Chemical Society, Perkin Transactions 2, 2001 , # 10 p. 1989 - 1997]

Anticonvulsant activity of oxindole derivatives and 1, 3-disubstituted indoles

[Gevorkyan, K. A.; Papayan, G. L.; Chshmarityan, S. G.; Paronikyan, R. G.; Akopyan, N. E. Pharmaceutical Chemistry Journal, 1988 , vol. 22, # 10 p. 765 - 769 Khimiko-Farmatsevticheskii Zhurnal, 1988 , vol. 22, # 10 p. 1203 - 1207]

Au/Ag-cocatalyzed aldoximes to amides rearrangement under solvent-and acid-free conditions

[Ramon, Ruben S.; Bosson, Johann; Diez-Gonzalez, Silvia; Marion, Nicolas; Nolan, Steven P. Journal of Organic Chemistry, 2010 , vol. 75, # 4 p. 1197 - 1202]

Iminoxyl radicals and stable products from the one-electron oxidation of 1-methylindole-3-carbaldehyde oximes

Isocyanatophosphoryl dichloride as reagent for introduction of carbamoyl group into molecules of π-excessive heterocycles and enamines

Abstract

Related Articles:

More Articles...