Conversion of imidoyl chlorides to imines. A new method for the acyl exchange and cleavage of amides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Hydrolysis of imidate esters derived from weakly basic amines. Influences of structure and pH on the partitioning of tetrahedral intermediates
2. Modifikationen von Antibiotika. 2. Mitteilung [1]. Über die Darstellung von 7-Amino-cephalosporansäure
3. Cleavage of 7α-methoxycephalosporin c derivatives with phosphorus pentachloride
4. Solvolyse von Carbonsäurederivaten, II. Hydrolyse von Carbonsäure‐imidchloriden
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1. Reduction of Carboxylic Acids to Aldehydes by Metal Hydrides;Comprehensive Organic Synthesis;1991
2. Reaction of pyrrolo[2,1-c][1,4]benzodiazepine-2,5,11-triones with phosphorus oxychloride;Tetrahedron Letters;1989
3. Synthesis of ketimines via palladium complex-catalyzed cross-coupling of imidoyl chlorides with organotin compounds;Tetrahedron Letters;1985-01
4. A new and mild method for the reduction of secondary amides to carbinolamine ethers and imines: a conversion of oxotomaymycin to tomaymycin;Tetrahedron Letters;1983-01
5. Enamines: recent advances in synthetic, spectroscopic, mechanistic, and stereochemical aspects—II;Tetrahedron;1982-01
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