Hypervalent iodine in organic synthesis. A new route to α-functionalized carboxylate esters.
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (29) , 2747-2750
- https://doi.org/10.1016/s0040-4039(01)90541-6
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Oxidative displacement of hypervalent iodine from alkyl iodidesJournal of the Chemical Society, Perkin Transactions 1, 1980
- Efficient Methods for Oxidation of AlcoholsBulletin of the Chemical Society of Japan, 1977
- The Synthesis of α-Hydroxycarboxylic Acids by Aeration of Lithiated Carboxylic Acids in Tetrahydrofuran SolutionSynthesis, 1971
- Metalated carboxylic acids. II. Monoalkylation of metalated toluic acids and dimethylbenzoic acidsJournal of the American Chemical Society, 1970
- Metalated carboxylic acids. III. Monoalkylation of alkylacetic acids. Possible alternative to the malonic ester synthesis for the preparation of dialkylacetic acidsJournal of the American Chemical Society, 1970
- .alpha.-Anions of carboxylic acids. I. Effect of hexamethylphosphoramide on metalation and alkylationThe Journal of Organic Chemistry, 1970
- Reaction of alkyl iodides with peracetic acid in the presence of aromatic compoundsThe Journal of Organic Chemistry, 1969
- Novel Reactions of Iodosobenzene with Various Organic CompoundsBulletin of the Chemical Society of Japan, 1968
- Metalated carboxylic acids. I. AlkylationJournal of the American Chemical Society, 1967
- CXL.—The bromination of acids in the α-positionJournal of the Chemical Society, Transactions, 1922