
Classics in Total Synthesis II
More Targets, Strategies, Methods
Wiley-VCH (Publisher)
1st Edition
Published on 12. September 2003
Book
Paperback/Softback
XIX, 639 pages
978-3-527-30684-8 (ISBN)
Description
Classics in Total Synthesis II is the long awaited sequel to Classics in Total Synthesis, a book that has made its mark as a superb tool for educating students and practitioners alike in the art of organic synthesis since its introduction in 1996. In this highly welcomed new volume, K. C. Nicolaou and Scott A. Snyder discuss in detail the most impressive accomplishments in natural product total synthesis during the 1990s and the first years of the 21st century. While all of the features that made the first volume of Classics so popular and unique as a teaching tool have been maintained, in this new treatise the authors seek to present the latest techniques and advances in organic synthesis as they beautifully describe the works of some of the most renowned synthetic organic chemists of our time.
· domino reactions, cascade sequences, biomimetic strategies, and asymmetric catalysis are systematically developed through the chosen synthesis
· cutting edge synthetic technologies are discussed in terms of mechanism and scope
· new reactions, such as olefin metathesis, are presented in mini-review style
· abundant references are given for further reading
Graduate students, educators, and researchers in the fields of synthetic and medicinal chemistry will wish to have a copy of this book in their collection as an indispensable companion that both augments and supplements the original Classics in Total Synthesis.
From reviews of "Classics in Total Synthesis":
"... a volume, (..) which any chemist with an interest in synthetic organic chemistry will wish to acquire."
JACS
"...this superb book (..) will be an essential purchase for many organic chemists."
Nature
· domino reactions, cascade sequences, biomimetic strategies, and asymmetric catalysis are systematically developed through the chosen synthesis
· cutting edge synthetic technologies are discussed in terms of mechanism and scope
· new reactions, such as olefin metathesis, are presented in mini-review style
· abundant references are given for further reading
Graduate students, educators, and researchers in the fields of synthetic and medicinal chemistry will wish to have a copy of this book in their collection as an indispensable companion that both augments and supplements the original Classics in Total Synthesis.
From reviews of "Classics in Total Synthesis":
"... a volume, (..) which any chemist with an interest in synthetic organic chemistry will wish to acquire."
JACS
"...this superb book (..) will be an essential purchase for many organic chemists."
Nature
Reviews / Votes
Abstract in:Journal of the American Chemistry Society, Vol. 126 No. 14
More details
Edition
1. Auflage
Language
English
Place of publication
Berlin
Germany
Target group
Professional and scholarly
Organiker, Studenten der Chemie, Chemische Industrie
Illustrations
339
339 s/w Abbildungen
Dimensions
Height: 25 cm
Width: 19 cm
Thickness: 2.8 cm
Weight
1454 gr
ISBN-13
978-3-527-30684-8 (9783527306848)
Schweitzer Classification
Other editions
Additional editions

Book
09/2003
1st Edition
Wiley-VCH
€119.00
Article exhausted; check for reprint
Previous edition

Book
09/2003
1st Edition
Wiley-VCH
€119.00
Article exhausted; check for reprint
Persons
K. C. Nicolaou is Professor of Chemistry at the University of California, San Diego and is Chairman of the Department of Chemistry and holds the Skaggs Professorship of Chemical Biology and the Darlene Shiley Chair in Chemistry at The Scripps Research Insitute. His impact on chemistry flows from his works in chemical synthesis and chemical biology described in over 550 publications and 55 patents.
S. A. Snyder is a Professor of Chemistry at the University of Chicago. His research interests include Chemical Biology and Organic Chemistry.
S. A. Snyder is a Professor of Chemistry at the University of Chicago. His research interests include Chemical Biology and Organic Chemistry.
Author
The Scripps Research Institute, La Jolla, USA
The Scripps Research Institute, La Jolla, USA
Content
Introduction
Isochrysohermidin (Boger)
Swinholide A (Paterson)
Dynemicin A (Myers)
Ecteinascidin 743 (Corey)
Resiniferatoxin (Wender)
Epothilone A (Nicolaou)
Manzamine A (Winkler/Martin)
Vancomycin (Nicolaou/Evans)
Everninomicin 13,384-1 (Nicolaou)
Bisorbicillinoids (Nicolaou)
Aspidophytine (Corey)
CP-Molecules (Nicolaou)
Colombiasin A (Nicolaou)
Quinine (Stork)
Longithorone A (Shair)
FR-182877 (Sorensen)
Vinblastine (Fukuyama)
Quarigemine C and Psycholeine (Overman)
Diazonamide A (Nicolaou)
Plicamine (Ley)
Isochrysohermidin (Boger)
Swinholide A (Paterson)
Dynemicin A (Myers)
Ecteinascidin 743 (Corey)
Resiniferatoxin (Wender)
Epothilone A (Nicolaou)
Manzamine A (Winkler/Martin)
Vancomycin (Nicolaou/Evans)
Everninomicin 13,384-1 (Nicolaou)
Bisorbicillinoids (Nicolaou)
Aspidophytine (Corey)
CP-Molecules (Nicolaou)
Colombiasin A (Nicolaou)
Quinine (Stork)
Longithorone A (Shair)
FR-182877 (Sorensen)
Vinblastine (Fukuyama)
Quarigemine C and Psycholeine (Overman)
Diazonamide A (Nicolaou)
Plicamine (Ley)