The rhodium(II)-catalyzed assembly of densely-substituted cis-configured cyclopropyl ethers by decarbenation of cycloheptatrienes is reported. At higher temperature, these non-acceptor cyclopropanes open to give all-E trienes under the same catalytic system, in a one-pot procedure. Experimental and computational studies show that, for the formation of all-E trienes, the cyclopropanes undergo first a Rh(II)-catalyzed cis- to trans-isomerization, followed by C–C bond cleavage.
Mato, M.; García-Morales, C.; Echavarren, A. M.
ACS Catal. 2020, 10 (6), 3564–3570
DOI:
10.1021/acscatal.0c00006
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