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Description for Organic Reactions
Hardcover. Part of a series of volumes, each of which is devoted to a single organic reaction, or a definite phase of a reaction. This volume discusses chiral synthons by ester hydrolysis catalyzed by pig liver esterase, and the electrophilic substitution of allysilanes and vinylsilanes. Series: Organic Reactions. Num Pages: 608 pages, tables, index. BIC Classification: PNN. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly. Dimension: 233 x 161 x 37. Weight in Grams: 952.
The volumes of Organic Reactions are collections of chapters each devoted to a single reaction, or a definite phase of a reaction, of wide applicability. The material is treated from a preparative viewpoint, with emphasis on limitations, interfering influences, effects of structure, and the selection of experimental techniques. Numerous detailed procedures illustrate the significant modifications of each method. Includes tables that contain all possible examples of the reaction under consideration.
The volumes of Organic Reactions are collections of chapters each devoted to a single reaction, or a definite phase of a reaction, of wide applicability. The material is treated from a preparative viewpoint, with emphasis on limitations, interfering influences, effects of structure, and the selection of experimental techniques. Numerous detailed procedures illustrate the significant modifications of each method. Includes tables that contain all possible examples of the reaction under consideration.
Product Details
Format
Hardback
Publication date
1989
Publisher
John Wiley & Sons Inc United States
Number of pages
608
Condition
New
Series
Organic Reactions
Number of Pages
608
Place of Publication
New York, United States
ISBN
9780471501695
SKU
V9780471501695
Shipping Time
Usually ships in 15 to 20 working days
Ref
99-15
About Kende
Andrew S. Kende, Charles F. Houghton Professor of Chemistry, Emeritus PhD, Harvard University, 1957. Professor Kende’s research interests include the total synthesis of alkaloids, terpenes, and antibiotics; rearrangement reactions; synthesis of antineoplastic natural products; chemistry of small rings; chemical and biochemical studies of polyhalogenated xenobiotics and of bacterial autoinducers.
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