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Hydroboration and Organic Synthesis : 9-Borabicyclo [3.3.1] nonane (9-BBN)

Hydroboration and Organic Synthesis : 9-Borabicyclo [3.3.1] nonane (9-BBN)

Softcover reprint of hardcover 1st Edition 2007

Paperback (14 Oct 2010)

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Publisher's Synopsis

9-Borabicyclo [3.3.1]nonane, a commercially available reagent, is the most versatile hydroborating reagent to synthesize organoboranes (B-R-9-BBN). The reagent exhibits remarkable regio-, chemo-, and stereoselectivity during hydroboration reactions. The organoboranes can be converted to C-H, C-O, C-N, C-S, C-halogen, C-metal and above all C-C bonds. In addition, the suitable substituted / unsaturated R of B-R-9-BBN can be utilized to produce dienes, enynes, allenes etc. with defined stereochemistry. 9-BBN's derivatives have been elegantly used for the asymmetric reduction of ketone moiety. Diels-Alder and Suzuki reactions have expanded the utility of 9-BBN for the synthesis of a variety of organic compounds required for industry. Consequently, this vast field in the form of a book will be helpful to synthetic organic chemists for easy access to literature, required for chemical transformations.

Book information

ISBN: 9783642080340
Publisher: Springer Berlin Heidelberg
Imprint: Springer
Pub date:
Edition: Softcover reprint of hardcover 1st Edition 2007
Language: English
Number of pages: 586
Weight: 908g
Height: 234mm
Width: 156mm
Spine width: 30mm