RT Journal Article
T1 Enantio- and Diastereoselective Copper-Catalyzed Allylboration of Alkynes with Allylic gem-Dichlorides
A1 Chaves Pouso, Andrea
A1 Álvarez-Constantino, Andrés M.
A1 Fañanás-Mastral, Martín
K1 Asymmetric catalysis
K1 Carboboration
K1 Copper
K1 gem-Dichlorides
K1 Skipped Dienes
AB A highly chemo-, regio-, enantio- and diastereoselective coupling of terminal alkynes, bis(pinacolato)diboron and allylic gem-dichlorides is reported. The method uses a chiral NHC−Cu catalyst which generates, in a single step, synthetically versatile chiral skipped dienes bearing a Z-alkenyl chloride, a trisubstituted E-alkenyl boronate and a bis-allylic stereocenter. Allylic gem-dichlorides are shown to be efficient substrates for catalytic asymmetric allylboration of alkynes. The method employs a chiral NHC−Cu catalyst capable of generating in a single step chiral skipped dienes bearing a Z-alkenyl chloride, a trisubstituted E-alkenyl boronate and a bis-allylic stereocenter with excellent levels of chemo-, regio- enantio- and diastereoselectivity. This high degree of functionalization makes these products versatile building blocks as illustrated with the synthesis of several optically active compounds. DFT calculations support the key presence of a metal cation bridge ligand–substrate interaction and account for the stereoselectivity outcome
PB Wiley
YR 2022
FD 2022
LK http://hdl.handle.net/10347/29234
UL http://hdl.handle.net/10347/29234
LA eng
NO Angew. Chem.Int. Ed.2022,61,e202117696
NO Financial support from the AEI (PID2020-118237RB-I00), Xunta de Galicia (ED431C 2018/04; Centro singular de investigación de Galicia accreditation 2019–2022, ED431G 2019/03) and the European Union (European Regional Development Fund - ERDF) is gratefully acknowledged. A. M. A.-C. thanks Xunta de Galicia for a predoctoral fellowship.
DS Minerva
RD 25 abr 2026