MIDA–Vinylsilanes: Selective Cross-Couplings and Applications to the Synthesis of Functionalized Stilbenes


Autoria(s): McLaughlin, Mark G.; McAdam, Catherine A.; Cook, Matthew J.
Data(s)

2015

Resumo

A rapid and stereodefined synthesis of MIDA−boryl vinylsilanes has been achieved through the hydrosilylation of an alkynylboronic ester. The E products which contain a silyl and boryl group can be selectively cross-coupled in a two-step bidirectional sequence to provide a rapid and high-yielding synthesis of complex styrenes.

Identificador

http://pure.qub.ac.uk/portal/en/publications/midavinylsilanes-selective-crosscouplings-and-applications-to-the-synthesis-of-functionalized-stilbenes(97c2ad08-e6c1-444d-9cd9-5f9cbb57d506).html

http://dx.doi.org/10.1021/ol503065a

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

McLaughlin , M G , McAdam , C A & Cook , M J 2015 , ' MIDA–Vinylsilanes: Selective Cross-Couplings and Applications to the Synthesis of Functionalized Stilbenes ' Organic Letters , vol 17 , no. 1 , pp. 10-13 . DOI: 10.1021/ol503065a

Tipo

article