Journal of the American Chemical Society

THE STRUCTURE OF ENOL-ACETATES AND THE CORRESPONDING VINYLAMINES

LJ Roll, R Adams

Index: Roll; Adams Journal of the American Chemical Society, 1931 , vol. 53, p. 3469,3474

Full Text: HTML

Citation Number: 4

Abstract

At present there has been only one method devised for the determination of the structure of enols where two or more structures are possible. This is the ozonization method of ScheiberI3 which consists merely in ozonizing any particular enol or equilibrium mixture of a keto and enol, and, after decomposing in the usual way, determining the structure of the products. There are in many instances, difficulties in the application of this method since it ...

Related Articles:

Clean and selective oxidation of aromatic alcohols using silica-supported Jones' reagent in a pressure-driven flow reactor

[Wiles, Charlotte; Watts, Paul; Haswell, Stephen J. Tetrahedron Letters, 2006 , vol. 47, # 30 p. 5261 - 5264]

Indium metal as a reducing agent in organic synthesis

[Pitts; Harrison; Moody Journal of the Chemical Society. Perkin Transactions 1, 2001 , # 9 p. 955 - 977]

Regioselective hydration of alkynes by iron (III) Lewis/Brønsted catalysis

[Cabrero-Antonino, Jose R.; Leyva-Perez, Antonio; Corma, Avelino Chemistry - A European Journal, 2012 , vol. 18, # 35 p. 11107 - 11114]

Direct synthesis of arylketones by nickel-catalyzed addition of arylboronic acids to nitriles

[Wong, Ying-Chieh; Parthasarathy, Kanniyappan; Cheng, Chien-Hong Organic Letters, 2010 , vol. 12, # 8 p. 1736 - 1739]

Green oxidations. The use of potassium permanganate supported on manganese dioxide

[Shaabani, Ahmad; Mirzaei, Peiman; Naderi, Soheila; Lee, Donald G. Tetrahedron, 2004 , vol. 60, # 50 p. 11415 - 11420]

More Articles...