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Hydroboration and Organic Synthesis || Synthesis of α-Bromoboranes

✍ Scribed by ,

Book ID
118135621
Publisher
Springer Berlin Heidelberg
Year
2007
Tongue
German
Weight
123 KB
Edition
2007
Category
Article
ISBN
3540490752

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✦ 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.

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