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Rhodium-Catalyzed Asymmetric Conjugate Addition of Organoboronic Acids to Nitroalkenes Using Chiral Bicyclo[3.3.0] Diene Ligands
Old before I diene: An efficient rhodium/diene‐catalyzed asymmetric conjugate addition of organoboronic acids to challenging nitroalkene substrates that lack α substituents has been developed. Chiral bicyclo[3.3.0] dienes were found to be superior ligands under ArB(OH)2/KHF2 conditions. Np=naphthyl....
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Published in: | Angewandte Chemie (International ed.) 2010-08, Vol.49 (33), p.5780-5783 |
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container_end_page | 5783 |
container_issue | 33 |
container_start_page | 5780 |
container_title | Angewandte Chemie (International ed.) |
container_volume | 49 |
creator | Wang, Zhi-Qian Feng, Chen-Guo Zhang, Shu-Sheng Xu, Ming-Hua Lin, Guo-Qiang |
description | Old before I diene: An efficient rhodium/diene‐catalyzed asymmetric conjugate addition of organoboronic acids to challenging nitroalkene substrates that lack α substituents has been developed. Chiral bicyclo[3.3.0] dienes were found to be superior ligands under ArB(OH)2/KHF2 conditions. Np=naphthyl. |
doi_str_mv | 10.1002/anie.201001883 |
format | article |
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source | Wiley-Blackwell Read & Publish Collection |
subjects | Alkenes - chemistry asymmetric catalysis Boronic Acids - chemistry Bridged Bicyclo Compounds - chemistry Catalysis conjugate addition diene ligands Isoquinolines - chemical synthesis Isoquinolines - chemistry Ligands nitroalkenes rhodium Rhodium - chemistry Stereoisomerism |
title | Rhodium-Catalyzed Asymmetric Conjugate Addition of Organoboronic Acids to Nitroalkenes Using Chiral Bicyclo[3.3.0] Diene Ligands |
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