Hydroboration and Organic Synthesis: 9-Borabicyclo [3.3.1] nonane (9-BBN) by Ranjit S. Dhillon (Repost) - ISBN:3540490752

Hydroboration and Organic Synthesis: 9-Borabicyclo [3.3.1] nonane (9-BBN) by Ranjit S. Dhillon (Repost)

Date: 10 November 2010, 05:07

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Hydroboration and Organic Synthesis: 9-Borabicyclo [3.3.1] nonane (9-BBN) by Ranjit S. Dhillon (Repost)
Publisher: Springer; 1 edition (June 28, 2007) | ISBN: 3540490752 | Pages: 586 | PDF | 20.06 MB

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.

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