The Total Synthesis of Natural Products, Volume 8

ISBN-13: 9780471545071 / Angielski / Twarda / 1992 / 720 str.

ApSimon; John W. ApSimon

Opis

A reference work which details synthetic approaches to a wide variety of natural products, this book includes details of the synthesis of spiroketal-containing natural products, tri-and tetracyclic diterpenes, polysaccharides and naturally-occurring quinones.

Spis treści

The Total Synthesis of Tri– and Tetracyclic Diterpenes (D. Goldsmith).

The Synthesis of Polysaccharides to 1986 (N. Kochetkov).

The Total Synthesis of Naturally Occurring Quinones (R. Thomson).

The Total Synthesis of Spiroketal–Containing Natural Products (V. Vaillancourt, et al.).

Index.

O autorze

About the editor JOHN APSIMON is Professor of Chemistry and Dean of Research and Graduate Studies at Carleton University. Dr. ApSimon is a former Senior Editor of the Canadian Journal of Chemistry and the Editor of the Wiley–Liss Journal Natural Toxins. Dr. ApSimon received his PhD in organic chemistry from the University of Liverpool.

Blurb

Organic chemistry′s innovative breadth is especially noteworthy in the area of natural products synthesis. Since the early 1970s, this landmark chemical reference has been documenting the newest and most important of these, in a readily understood format, that clearly traces each of their synthetic routes. Volume Eight, the latest in the series, contains a long–awaited look at the synthesis of tri– and tetracyclic diterpenes, along with the synthesis of naturally occurring quinones. Recent interest in the biologically important polysaccharides has led to a detailed consideration of that compound class. Finally, this new volume contains a look at the strategies and methods specific to natural products containing the spiroketal functional group. The Total Synthesis of Natural Products, Volume Eight, continues the meticulous work of the series, providing chemists with an entirely up–to–date and convenient guide to the critical new syntheses essential to organic chemistry′s continuing evolution.