A new reagent for the methylation of carboxyl groups
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Higher Alkyl Sulfonates
2. Facile synthesis of methanesulfonate esters
3. The total synthesis of (±)-decinine
4. Modification of .ALPHA.-santonin. I. An abnormal chlorination of 3-hydroxy-4,5-epoxy-6,11.BETA.H-eudesm-1-en-6,12-olide with methanesulfonyl chloride.
5. Model studies directed toward the total synthesis of vernolepin: construction of the α-methylene-δ-lactone portion of vernolepin.
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1. Structure–Affinity Relationships of 2,3,4,5-Tetrahydro-1H-3-benzazepine and 6,7,8,9-Tetrahydro-5H-benzo[7]annulen-7-amine Analogues and the Discovery of a Radiofluorinated 2,3,4,5-Tetrahydro-1H-3-benzazepine Congener for Imaging GluN2B Subunit-Containing N-Methyl-d-aspartate Receptors;Journal of Medicinal Chemistry;2019-10-28
2. Protection for the Carboxyl Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
3. ChemInform Abstract: A New Reagent for the Methylation of Carboxyl Groups.;ChemInform;2010-05-22
4. Preparation of Esters;Compendium of Organic Synthetic Methods;2008-04-22
5. Methanesulfonyl chloride;Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15
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