{"product_id":"9783642080340","title":"Hydroboration and Organic Synthesis: 9-Borabicyclo [3.3.1] nonane (9-BBN)","description":"\u003ch1\u003eHydroboration and Organic Synthesis: 9-Borabicyclo [3.3.1] nonane (9-BBN)\u003c\/h1\u003e \u003ch2\u003eDhillon, Ranjit S.\u003c\/h2\u003e \u003cp\u003e\u003c\/p\u003e\u003cp\u003e9-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.\u003c\/p\u003e \u003ch3\u003eDetails\u003c\/h3\u003e \u003cp\u003ePublished by: Springer\u003c\/p\u003e \u003cp\u003ePublication Date: 2010-10-14\u003c\/p\u003e \u003cp\u003eFormat: Paperback\u003c\/p\u003e \u003cp\u003eISBN-13: 9783642080340\u003c\/p\u003e \u003cp\u003eDOI: 10.1007\/978-3-540-49076-0\u003c\/p\u003e \u003cp\u003eDimensions: 235cm x155cm\u003c\/p\u003e \u003cp\u003ePages: 586\u003c\/p\u003e ","brand":"Springer Berlin Heidelberg","offers":[{"title":"Default Title","offer_id":50148711956620,"sku":"9783642080340","price":197.99,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0710\/9545\/1788\/files\/9783642080340.jpg?v=1779567553","url":"https:\/\/lateknightbooks.com\/products\/9783642080340","provider":"Late Knight Books and Services, LLC","version":"1.0","type":"link"}