Stereodivergent Synthesis through Catalytic Asymmetric Reversed Hydroboration
journal contributionposted on 26.02.2019, 00:00 by Tao-Tao Gao, Wen-Wen Zhang, Xin Sun, Hou-Xiang Lu, Bi-Jie Li
The control of chemo-, regio-, diastereo-, and enantioselectivity is a central theme in organic synthesis. The capability to obtain the full set of stereoisomers of a molecule would significantly enhance the efficiency for the synthesis of natural product analogues and creation of chiral compound libraries for drug discovery. Despite the tremendous progress achieved in the field of asymmetric synthesis in the past decades, the precise control of both relative and absolute configurations in catalyst-controlled reactions that create multiple stereocenters remains a significant synthetic challenge. We report here the development of a catalyst-controlled hydroboration with hitherto unattainable selectivity. The Rh-catalyzed hydroboration of α, β-unsaturated carbonyl compounds with pinacolborane proceeds with high levels of regio-, diastereo-, and enantioselectivities to provide a hydroboration product with two vicinal stereocenters. Through the appropriate choice of substrate geometry (E or Z) and ligand enantiomer (S or R), all the possible diastereoisomers are readily accessible. The boron-containing products underwent many stereospecific transformations, thus providing a strategy for collective stereodivergent synthesis of diverse valuable chiral building blocks.
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product analoguesvicinal stereocentersdrug discoveryregioboron-containing productschiral building blockssubstrate geometrypinacolborane proceedsCatalytic Asymmetric Reversed Hydroborationcatalyst-controlled hydroborationStereodivergent Synthesisligand enantiomerRh-catalyzed hydroborationstereospecific transformationshydroboration productstereodivergent synthesisdiastereochiral compound librariescarbonyl compoundscatalyst-controlled reactions