Lewis Acid Reagents
A Practical Approach
Published on 28. January 1999
Book
Hardback
292 pages
978-0-19-850099-5 (ISBN)
Description
Many important Carbon-Carbon bond forming processes are catalyzed by Lewis acid reagents. There are important recent advances in Lewis acid chemistry. A variety of new selective organic syntheses are now available using modified/designed reagents. This book is a comprehensive laboratory guide which will prove invaluable to all organic chemists wishing to use these new Lewis acid reagents in modern organic synthesis. Both new and established chemists will find in this
book all the necessary information they need to enable them to exploit these powerful synthetic tools.
book all the necessary information they need to enable them to exploit these powerful synthetic tools.
More details
Series
Language
English
Place of publication
Oxford
United Kingdom
Target group
Professional and scholarly
Illustrations
numerous line figures
Dimensions
Height: 241 mm
Width: 160 mm
Thickness: 21 mm
Weight
585 gr
ISBN-13
978-0-19-850099-5 (9780198500995)
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
Professor Dr. Hisashi Yamamoto, Graduate School of Engineering, Nagoya University, Chikusa Nagoya 464-01, Japan Tel: 81 52 789 3331 j45988a@nucc.cc.nagoya-u.ac.jp
Content
1. Introduction ; 2. Synthetic utility of bulky aluminium reagents as Lewis acid receptors ; 3. Boron reagents ; 4. Magnesium (II) and other alkali and alkaline earth metals ; 5. Zinc (II) reagents ; 6. Chiral titanium complexes for enantioselective catalysis ; 7. Tin Lewis acid ; 8. Silicon (IV) reagents ; 9. Silver and gold reagents ; 10. Zr- and Hf-centred Lewis acid in organic synthesis ; 11. Scandium(III) and yttrium (III) reagents ; 12. Lanthanides (III) reagents ; 13. Other transition metal reagents: chiral transition-metal Lewis acid catalysis for asymmetric organic synthesis ; 14. Lewis acids-assisted anionic polymerizations for synthesis of polymers with controlled molecular weights