Functionalization of carboxylic anhydrides at α-carbon with hypervalent iodine reagents: one-pot conversion of anhydrides to 2-sulfonyloxycarboxylate esters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Dehydration-type Ti-Claisen Condensation (Carbonhomologation) of α-Heteroatom-substituted Acetates with Alkyl Formates: Utilization as (Z )-Stereodefined Cross-coupling Partners and Application to Concise Synthesis of Strobilurin A;Advanced Synthesis & Catalysis;2017-09-29
2. Hypervalent Iodine Reagents in Organic Synthesis;Hypervalent Iodine Chemistry;2013-10-04
3. Stereoselective Synthesis of γ-Lactams from Imines and Cyanosuccinic Anhydrides;Organic Letters;2013-09-26
4. A convenient one-pot synthesis of amines from aldoximes mediated by Koser’s reagent;Arkivoc;2011-01-17
5. ChemInform Abstract: Functionalization of Carboxylic Anhydrides at α-Carbon with Hypervalent Iodine Reagents: One-Pot Conversion of Anhydrides to 2-Sulfonyloxycarboxylate Esters.;ChemInform;2010-05-22
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