A Mild Approach toN-Acylformamidines andC-Acylamidines by the Facile Reduction of Carbodiimides with Pentacoordinated Silicon Hydrides

Autor:	Myriam Perrot-Petta, J. P. Corriu, null Robert, G. F. Lanneau
Rok vydání:	1991
Předmět:	Silicon Hydrosilylation Hydride medicine.drug_class Aryl Organic Chemistry chemistry.chemical_element Carboxamide Medicinal chemistry Catalysis Acylation Amidine Reduction (complexity) chemistry.chemical_compound chemistry medicine
Zdroj:	Synthesis. 1991:954-958
ISSN:	1437-210X 0039-7881
DOI:	10.1055/s-1991-28531
Popis:	N 1 -Acyl-, N 1 -aryl-N 2 -arylformamidines 4 and N 1 ,N 2 -dialkyl C-acylamidines 6 result from the acylation of the N 1 -silylformamidines 2a and C-silyl amidines 2 b,c respectively. The latter are obtained by the hydrosilylation of aryl- and alkylcarbodiimides with the pentacoordinated silicon hydride 1
Databáze:	OpenAIRE
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