Stereodivergent 1,3-difunctionalization of alkenes by charge relocation
Nature(2024)
摘要
Alkenes are indispensable feedstocks in chemistry. Functionalization at both carbons of the alkene—1,2-difunctionalization—is part of chemistry curricula worldwide 1 . Although difunctionalization at distal positions has been reported 2 – 4 , it typically relies on designer substrates featuring directing groups and/or stabilizing features, all of which determine the ultimate site of bond formation 5 – 7 . Here we introduce a method for the direct 1,3-difunctionalization of alkenes, based on a concept termed ‘charge relocation’, which enables stereodivergent access to 1,3-difunctionalized products of either syn - or anti -configuration from unactivated alkenes, without the need for directing groups or stabilizing features. The usefulness of the approach is demonstrated in the synthesis of the pulmonary toxin 4-ipomeanol and its derivatives.
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