
Organic Syntheses, Volume 71
Larry E. Overman(Editor)
Wiley (Publisher)
Will be published approx. on 5. October 1993
Book
Hardback
320 pages
978-0-471-30531-6 (ISBN)
Description
Consists of 30 checked and edited experimental procedures that illustrate new synthetic techniques or describe the preparation of particularly useful chemicals. Features procedures exemplifying important methods for preparing enantiomerically pure substances by asymmetric catalysis; details a reliable zirconium-based process for the coupling of alkynes and enones; concludes with the preparation of four useful starting materials. A section on waste disposal information is included.
More details
Series
Edition
Volume 71 edition
Language
English
Place of publication
New York
United States
Target group
College/higher education
Professional and scholarly
Product notice
sewn/stitched
Cloth over boards
Dimensions
Height: 236 mm
Width: 160 mm
Thickness: 21 mm
Weight
590 gr
ISBN-13
978-0-471-30531-6 (9780471305316)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Person
Larry Overman is Professor of Chemistry at the University of California at Irvine. He obtained a B.A. degree from Earlham College in 1965, and completed his doctoral dissertation in 1969 with Professor Howard W. Whitlock, Jr., at the University of Wisconsin. After a NIH postdoctoral fellowship with Professor Ronald Breslow at Columbia University, he joined the faculty at the University of California, Irvine, in 1971. Professor Overman's research interests center on the invention of new reactions and strategies in organic synthesis and the total synthesis of natural products and their congeners. Using synthesis strategies developed largely in his laboratory, Professor Overman's group has completed total syntheses of more than 80 structurally complex natural products.
Content
Partial table of contents:
Asymmetric Hydrogenation of 3-OXO Carboxylates Using BinaprutheniumComplexes: (R)-(-)-Methyl 3-Hydroxybutanoate (M. Kitamura, etal.).
Direct Degradation of the Biopolymer Poly [(R)-3-HydroxybutyricAcid] to (R)-3-Hydroxybutanoic Acid and Its Methyl Ester (D.Seebach, et al.).
3-(S)-[(tert-Butyldiphenylsilyl)-Oxy]-2-Butanone (L. Overman &G. Rishton).
Schwartz's Reagent (S. Buchwald, et al.).
4-Methoxy-4'-Nitrobiphenyl (J. Stille, et al.).
Ubiquinone-1 (Y. Naruta & K. Maruyama).
Benzoannelation of Ketones: 3,4-Cyclododeceno-1-Methylbenzene (M.Tius & G. Kannangara).
2-Methylene-1, 3-Dithiolane (K. Dahnke & L. Paquette).
Methoxycarbonylmethylation of Aldehydes Via Siloxycyclopropanes:Methyl 3,3-Dimethyl-4-Oxobutanoate (H.-U.
Reissig, et al.).
9-Bromo-9-Phenylfluorene (T. Jamison, et al.).
Indexes.
Asymmetric Hydrogenation of 3-OXO Carboxylates Using BinaprutheniumComplexes: (R)-(-)-Methyl 3-Hydroxybutanoate (M. Kitamura, etal.).
Direct Degradation of the Biopolymer Poly [(R)-3-HydroxybutyricAcid] to (R)-3-Hydroxybutanoic Acid and Its Methyl Ester (D.Seebach, et al.).
3-(S)-[(tert-Butyldiphenylsilyl)-Oxy]-2-Butanone (L. Overman &G. Rishton).
Schwartz's Reagent (S. Buchwald, et al.).
4-Methoxy-4'-Nitrobiphenyl (J. Stille, et al.).
Ubiquinone-1 (Y. Naruta & K. Maruyama).
Benzoannelation of Ketones: 3,4-Cyclododeceno-1-Methylbenzene (M.Tius & G. Kannangara).
2-Methylene-1, 3-Dithiolane (K. Dahnke & L. Paquette).
Methoxycarbonylmethylation of Aldehydes Via Siloxycyclopropanes:Methyl 3,3-Dimethyl-4-Oxobutanoate (H.-U.
Reissig, et al.).
9-Bromo-9-Phenylfluorene (T. Jamison, et al.).
Indexes.