Synthesis of 2-Alkynoates by Palladium(II)-Catalyzed Oxidative Carbonylation of Terminal Alkynes and Alcohols


Autoria(s): Cao, Qun; Hughes, N. Louise; Muldoon, Mark J.
Data(s)

01/08/2016

Resumo

A homogeneous PdII catalyst, utilizing a simple and inexpensive amine ligand (TMEDA), allows 2-alkynoates to be prepared in high yields by an oxidative carbonylation of terminal alkynes and alcohols. The catalyst system overcomes many of the limitations of previous palladium carbonylation catalysts. It has an increased substrate scope, avoids large excesses of alcohol substrate and uses a desirable solvent. The catalyst employs oxygen as the terminal oxidant and can be operated under safer gas mixtures.

Identificador

http://pure.qub.ac.uk/portal/en/publications/synthesis-of-2alkynoates-by-palladiumiicatalyzed-oxidative-carbonylation-of-terminal-alkynes-and-alcohols(04a2227d-f095-4d2d-8d14-816fbc4a1d29).html

http://dx.doi.org/10.1002/chem.201602558

Idioma(s)

eng

Direitos

info:eu-repo/semantics/closedAccess

Fonte

Cao , Q , Hughes , N L & Muldoon , M J 2016 , ' Synthesis of 2-Alkynoates by Palladium(II)-Catalyzed Oxidative Carbonylation of Terminal Alkynes and Alcohols ' Chemistry - A European Journal , vol 22 , no. 34 , pp. 11982–11985 . DOI: 10.1002/chem.201602558

Tipo

article