Author:
Katritzky Alan R.,El-Mowafy Azzahra M.
Publisher
American Chemical Society (ACS)
Cited by
8 articles.
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1. Mild, powerful, and robust methods for esterification, amide formation, and thioesterification between acid chlorides and alcohols, amines, thiols, respectively;Tetrahedron;2007-11
2. Water Solvent Method for Esterification and Amide Formation between Acid Chlorides and Alcohols Promoted by Combined Catalytic Amines: Synergy betweenN-Methylimidazole andN,N,N′,N′-Tetramethylethylenediamine (TMEDA);Advanced Synthesis & Catalysis;2006-10
3. Nucleophilic substitution at saturated carbon atoms. Mechanisms and mechanistic borderlines: Evidence from studies with neutral leaving groups;Journal of Physical Organic Chemistry;1988-01
4. Palladium-catalyzed decarbonylation of acyl cyanides;The Journal of Organic Chemistry;1986-03
5. Nucleophilic displacement with heterocycles as leaving groups. Part 16. Reactions of secondary alkyl primary amines with 5,6,8,9-tetrahydro-7-phenyldibenzo[c,h]xanthylium trifluoromethanesulphonate to give intermediates solvolysing without rearrangement;Journal of the Chemical Society, Perkin Transactions 2;1985