An efficient method for hydrolysis of N-monosubstituted amides via acetoxypivalimides
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (5) , 731-734
- https://doi.org/10.1016/s0040-4039(00)94615-x
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- A mild two-step method for the hydrolysis of lactams and secondary amidesThe Journal of Organic Chemistry, 1983
- Syntheses of the stereoisomers of the sex pheromones of the southern corn rootworm and lesser tea tortrixThe Journal of Organic Chemistry, 1982
- Synthesis of (±)-10-methyl-1-dodecanol acetate, the chiral component of the smaller tea tortrix moth (Adoxophyes sp.), with an option for asymmetric inductionJournal of Chemical Ecology, 1982
- Mild conversion of carboxamides and carboxylic acid hydrazides to acids and estersThe Journal of Organic Chemistry, 1981
- Asymmetric alkylation of amide anions. Product analysis by GLC using cholesteryl cinnamate, a liquid crystal phaseThe Journal of Organic Chemistry, 1980
- Preparative Scale Directed Resolution of Enantiomeric Carboxylic Acids and Lactones via Liquid Chromatography and Neighboring‐Group Assisted Hydrolysis of Diastereomeric AmidesAngewandte Chemie International Edition in English, 1979
- Natural Product Synthesis and Vitamin B 12Science, 1977
- Base-promoted hydrolysis of amides at ambient temperaturesJournal of the American Chemical Society, 1976
- Surfuranes. X. Reagent for the facile cleavage of secondary amidesJournal of the American Chemical Society, 1973
- The total synthesis of vitamin B12Pure and Applied Chemistry, 1973