Affiliation:
1. Department Química Física i Inorgànica Universitat Rovira i Virgili 43007 Tarragona Spain
2. Department Chemistry Edinburgh University EH8 9YL Edinburgh UK
Abstract
AbstractRegioselective borylcupration of borylated skipped (Z)‐dienes generates diborylated alkylcopper species that are involved in an intramolecular stereospecific B/Cu 1,3‐rearrangement by migration of Bpin moiety from C(sp2) to C(sp3). DFT mechanistic studies showed that boryl migration occurs through the formation of 4‐membered boracycle intermediate with a moderate free‐energy barrier. Moreover, the use of KOMe forms stable Lewis base adducts with Bpin moieties that blocks the reaction. Subsequently to the 1,3‐boron shift, the in situ electrophilic trapping allows selective C−H, C−C and C−X bonds, followed by intramolecular cross coupling giving access to cyclic functionalized alkylidenecyclohexanes or alkylidenecyclobutanes.
Subject
General Chemistry,Catalysis
Cited by
4 articles.
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