Hydroboration and Organic Synthesis : 9-Borabicyclo [3.3.1] nonane (9-BBN)
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-...
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| Autor principal: | |
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| Format: | Livre numérique |
| Idioma: | Anglais |
| Publicat: |
Berlin, Heidelberg :
Springer Berlin Heidelberg : Springer e-books
[20..].
Cham : Springer Nature |
| Accés en línia: | Accès sur la plateforme de l'éditeur Accès sur la plateforme Istex Accès Université d'Orléans Accès INSA CVL |
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Archives Springer e-books (Licence nationale) Archives Springer e-books (Licence nationale) |
| Autres localisations: | Voir dans le Sudoc |
| Edition sous un autre format: | • Hydroboration and organic synthesis, 9-borabicyclo[3.3.1]nonane (9-BBN), Ranjit S. Dhillon, Berlin, Springer-Verlag, 2007, 1 vol. (XIII-586 p), 978-3-540-49075-3 |
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| 100 | 1 | |a Dhillon, Ranjit S. | |
| 245 | 1 | 0 | |a Hydroboration and Organic Synthesis : |b 9-Borabicyclo [3.3.1] nonane (9-BBN) |c edited by Ranjit S. Dhillon. |
| 260 | |a Berlin, Heidelberg : |b Springer Berlin Heidelberg : |b Springer e-books. | ||
| 260 | |a Cham : |b Springer Nature, |c [20..]. | ||
| 500 | |a Archives Springer e-books (Licence nationale) | ||
| 500 | |a Archives Springer e-books (Licence nationale) | ||
| 505 | 1 | |a General Remarks Preparation and Properties Kinetic Studies Hydroboration Synthesis of Alcohols Synthesis of Aldehydes and Ketones Synthesis of Carboxylic Acids Synthesis of Esters Synthesis of Nitriles Synthesis of (E)-?,?-Unsaturated Amides Synthesis of Amines Synthesis of Halides Synthesis of Dialkylsulfides Synthesis of Thiophene Oligomers Synthesis of Cyclopropanes and Cyclobutanes Synthesis of Borinanes Synthesis and Transformations of Butterflyboranes: cis-Bicyclo[3.3.0]oct-1-yldialkylboranes Synthesis of ?-Bromoboranes Synthesis of Borinates Synthesis and Transformation of Polymers Synthesis of Alkali Metal 9-Boratabicyclo[3.3.1] nonane (Li, K, and Na 9-BBNH) Synthesis of B-R-9-BBN Not Available via Hydroboration Synthesis of Unsaturated Compounds Reduction Asymmetric Reduction Cleavage of Ethers trans-Metalation Separation of Isomers Diels-Alder Reaction Suzuki Reaction Miscellaneous Reactions | |
| 506 | |a Accès en ligne pour les établissements français bénéficiaires des licences nationales | ||
| 506 | |a Accès soumis à abonnement pour tout autre établissement | ||
| 506 | |a Conditions particulières de réutilisation pour les bénéficiaires des licences nationales. https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017 | ||
| 520 | |a 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 | ||
| 776 | 0 | |0 115636161 |t Hydroboration and organic synthesis |o 9-borabicyclo[3.3.1]nonane (9-BBN) |f Ranjit S. Dhillon |c Berlin |n Springer-Verlag |d 2007 |p 1 vol. (XIII-586 p) |z 978-3-540-49075-3 | |
| 856 | 4 | |q PDF |u https://doi.org/10.1007/978-3-540-49076-0 |z Accès sur la plateforme de l'éditeur | |
| 856 | 4 | |u https://revue-sommaire.istex.fr/ark:/67375/8Q1-K4S0SJW1-V |z Accès sur la plateforme Istex | |
| 856 | 4 | |5 452349901:74788465X |u https://ezproxy.univ-orleans.fr/login?url=https://doi.org/10.1007/978-3-540-49076-0 |z Accès Université d'Orléans | |
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