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Simple Method for the Esterification of Carboxylic Acids

B. Neises, +1 more
- 01 Jul 1978 - 
- Vol. 17, Iss: 7, pp 522-524
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This article is published in Angewandte Chemie.The article was published on 1978-07-01. It has received 1660 citations till now. The article focuses on the topics: Simple (abstract algebra).

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4-Dialkylaminopyridines as Highly Active Acylation Catalysts. [New synthetic method (25)]

TL;DR: The synthesis of 4-dialkylaminopyridines can be accomplished in two steps starting from pyridine as discussed by the authors, and these derivatives are approximately 104 times more active when used as acylation catalysts.
Journal ArticleDOI

Recent developments in methods for the esterification and protection of the carboxyl group

TL;DR: Some of the more recent innovations and techniques which have been developed in the past 10-15 years around these features of carboxyl group chemistry are discussed in this article, with a review.
Journal ArticleDOI

High-throughput profiling of protein N-glycosylation by MALDI-TOF-MS employing linkage-specific sialic acid esterification.

TL;DR: A rapid, robust and linkage-specific high-throughput method for sialic acid stabilization and MALDI-TOF-MS analysis, to allow direct modification of impure glycan-containing mixtures such as PNGase F-released human plasma N-glycome is established.
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The Pharmacology of Ryanodine and Related Compounds

TL;DR: Major advances have been made in developing chemical approaches that permit the structure of ryanodine to be derivatized in selective ways, and several of these changes have yielded compounds that differ in their binding affinities and in their abilities to modify the properties of the RyR channels.
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