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Asymmetric Diboration of Terminal Alkenes with a Rhodium Catalyst and Subsequent Oxidation: Enantioselective Synthesis of Optically Active 1,2-Diols
Pin it down: A highly enantioselective diboration of terminal alkenes with chiral 1 and bis(pinacolato)diboron (B2pin2) was realized. Subsequent oxidation of the diboron adducts with sodium peroxoborate readily gave the corresponding optically active 1,2‐diols in high yields and high enantioselectiv...
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Published in: | Angewandte Chemie International Edition 2013-10, Vol.52 (42), p.11011-11015 |
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container_title | Angewandte Chemie International Edition |
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creator | Toribatake, Kenji Nishiyama, Hisao |
description | Pin it down: A highly enantioselective diboration of terminal alkenes with chiral 1 and bis(pinacolato)diboron (B2pin2) was realized. Subsequent oxidation of the diboron adducts with sodium peroxoborate readily gave the corresponding optically active 1,2‐diols in high yields and high enantioselectivities. |
doi_str_mv | 10.1002/anie.201305181 |
format | article |
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source | Wiley-Blackwell Read & Publish Collection |
subjects | asymmetric catalysis boron diols enantioselectivity rhodium |
title | Asymmetric Diboration of Terminal Alkenes with a Rhodium Catalyst and Subsequent Oxidation: Enantioselective Synthesis of Optically Active 1,2-Diols |
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