The Reaction of Aromatic Nitro-and Nitroso Compounds with Sodium Alcoholates
Author : William Orlin Kenyon
Publisher :
Page : pages
File Size : 49,8 MB
Release : 1931
Category :
ISBN :
Author : William Orlin Kenyon
Publisher :
Page : pages
File Size : 49,8 MB
Release : 1931
Category :
ISBN :
Author : Chester Merle Suter
Publisher :
Page : 16 pages
File Size : 17,94 MB
Release : 1927
Category : Nitro-compounds
ISBN :
Author : Morgan J. Rarick
Publisher :
Page : pages
File Size : 36,25 MB
Release : 1939
Category :
ISBN :
Author : Henry Feuer
Publisher : John Wiley & Sons
Page : 792 pages
File Size : 29,51 MB
Release : 1969-01-15
Category : Science
ISBN :
Author : Henry Feuer
Publisher :
Page : 474 pages
File Size : 34,55 MB
Release : 1969
Category : Nitro compounds
ISBN :
Author : Chester Merle Suter
Publisher :
Page : pages
File Size : 10,54 MB
Release : 1926
Category :
ISBN :
Author : Barry M. Trost
Publisher : Elsevier
Page : 1174 pages
File Size : 44,64 MB
Release : 1991
Category : Science
ISBN : 9780080405995
Volume 8.
Author : Stanley R. Sandler
Publisher : Elsevier
Page : 563 pages
File Size : 41,42 MB
Release : 2012-12-02
Category : Science
ISBN : 008092557X
Volume II describes 17 additional functional groups and presents a critical review of their available methods of synthesis with preparative examples of each. Attention is especially paid to presenting specific laboratory directions for the many name reactions used in describing the synthesis of these functional groups. - This volume covers synthetic methods for the generation of 17 functional groups; Unique features include the citation of U.S. and foreign patent literature and safety information; Major topics discussed: Ynamines, Enamines, Allenes, Azo compounds, Azoxy compounds, N-Nitroso compounds
Author : Barry M. Trost
Publisher : Elsevier
Page : 1166 pages
File Size : 30,69 MB
Release : 1992-09-08
Category : Science
ISBN : 0080912516
This volume contains 37 chapters on methods for reducing functional groups, organized into four main parts. (i) Reduction of C=X systems, where X is an electronegative heteroatom, divided into 14 chapters based on the degree of reduction, the oxidation level of the C=X substrate, and on the nature of the reagent. (ii) Reduction of X=Y systems, divided into three chapters, covering the reduction of such groups as nitro, azo, and the various kinds of P=O and S=O groups. (iii) Reduction of C=C and C≡C, divided into 12 chapters based on the method of reduction, with aromatic, heteroaromatic, and conjugated systems treated separately, and including an extensive discussion of hydrometallation. (iv) Reduction of single bonds, C-X to C-H, in eight chapters, including the hydrogenolysis of the various kinds of C-X bonds, the reduction of epoxides, and the reduction of vinyl derivatives to alkenes. Each chapter includes a discussion of chemoselectivity, regioselectivity, and stereoselectivity, wherever it is appropriate, and most include advice on the reagent of choice, and the mechanistic basis of the various methods of reduction. In short, it is, within the space available, as near to a comprehensive account of reduction in organic chemistry as one could hope for.
Author : Ludwig Gattermann
Publisher :
Page : 434 pages
File Size : 38,46 MB
Release : 1914
Category : Chemistry, Organic
ISBN :