Literature DB >> 25513732

MIDA-vinylsilanes: selective cross-couplings and applications to the synthesis of functionalized stilbenes.

Mark G McLaughlin1, Catherine A McAdam, Matthew J Cook.   

Abstract

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.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 25513732     DOI: 10.1021/ol503065a

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

Review 1.  Sequential and iterative Pd-catalyzed cross-coupling reactions in organic synthesis.

Authors:  Patrick Dobrounig; Melanie Trobe; Rolf Breinbauer
Journal:  Monatsh Chem       Date:  2016-12-09       Impact factor: 1.451

2.  A Convenient, Rapid, Conventional Heating Route to MIDA Boronates.

Authors:  Andrew McGown; Anthony K Edmonds; Daniel Guest; Verity L Holmes; Chris Dadswell; Ramón González-Méndez; Charles A I Goodall; Mark C Bagley; Barnaby W Greenland; John Spencer
Journal:  Molecules       Date:  2022-08-09       Impact factor: 4.927

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.