RT Journal Article
T1 Transition-Metal-Free Direct anti-Carboboration of Alkynes with  Boronic Acids To Produce Alkenylheteroarenes
A1 Roscales García, Silvia
A1 García Csaky, Aurelio
AB The transition-metal-free intermolecular direct 1,2-carboboration reaction of heteroarylacetylenes using boronic acids as reagents is achieved by utilizing tartaric acid as promoter. The reaction proceeds with excellent regioselectivity and anti stereoselectivity to afford boroxole frameworks. The resulting compounds are of use for the stereoselective preparation of polysubstituted alkenylheteroarenes.
PB American Chemical Society
YR 2015
FD 2015
LK https://hdl.handle.net/20.500.14352/116175
UL https://hdl.handle.net/20.500.14352/116175
LA eng
NO Roscales, Silvia, y Aurelio G. Csákÿ. «Transition-Metal-Free Direct Anti -Carboboration of Alkynes with Boronic Acids To Produce Alkenylheteroarenes». Organic Letters, vol. 17, n.o 6, marzo de 2015, pp. 1605-08. DOI.org (Crossref), https://doi.org/10.1021/acs.orglett.5b00517.
NO Universidad Complutense de Madrid
DS Docta Complutense
RD 7 abr 2025