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

Content Provider	Springer-eBooks
Author	Dhillon, Ranjit S.
Copyright Year	2007
Abstract	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.
File Format	PDF
ISBN	9783540490760
Language	English
Publisher	SpringerLink Springer eBooks
Access Restriction	Subscribed
Subject Keyword	Chemistry Organic Chemistry Medicinal Chemistry Biochemistry, general
Content Type	Text
Resource Type	Book