Facile and stereoselective synthesis of vinylphosphonates

DOI: 10.1016/S0022-328X(96)06646-6

Source and publish data:

Journal of Organometallic Chemistry p. 301 - 311 (1997)

Update date:2022-09-26

Topics:

Authors:

Cristau, Henri-Jean

Mbianda, Xavier Yangkou

Beziat, Yves

Gasc, Marie-Benedicte

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0022-328X(96)06646-6

Stereoselective syntheses of mono-, di- and trisubstituted diethyl alk-1-enylphosphonates, starting from readily available alk-1-ynylphosphonates, have been developed, using catalytic hydrogenation or cuprate addition on the triple bond.

Full text of DOI:10.1016/S0022-328X(96)06646-6

Products guided by the article

Product name:diethyl 1-methyl-2-phenyl-hex-1(Z)-enylphosphonate

Cas No:190772-84-0

R&D Labs maybe for 190772-84-0

Luojiang Chenming Biological Products Co

Contact:+86 15000297032

Address:GROUP NO.4, HE SHENG VILLAGE, PANLONG TOWN,
Anhui New Star Pharmaceutical Development Co., Ltd

Contact:013956922763

Address:Floor 3, F9A, F Workshop, No.110 Kexue Road, High-Tech Development Zone, Hefei, Anhui ,China
Shanghai Yurui Biotechnology(Anyang) Pharmaceutical Co., Ltd

Contact:+86-0372-3662335 +86-0372-3661988

Address:hanling industrial park anyang
Jiande City Silibase Silicone New Material Manufacture Co., Ltd.

Contact:15967177856

Address:Genglou Industrial Development Area
SuZhou Bichal Biological Technology CO.,LTD

Contact:+86-512-68051130

Address:NO.32 huoju road HI-TECH Industrial development zone SuZhou China

Relevant to this article

5-[Aryloxypyridyl (or nitrophenyl)]-4H-1,2,4-triazoles as novel flexible benzodiazepine analogues: Synthesis, receptor binding affinity and lipophilicity-dependent anti-seizure onset of action

Doi:10.1016/j.bioorg.2020.104504
(2021)
Photophysical studies of some heterocyclic chromophores as potential NLO materials

Doi:10.1016/j.saa.2011.12.031
(2012)
Selective synthesis of 1,4,5-trisubstituted imidazoles from α-imino ketones prepared by N-heterocyclic-carbene-catalyzed aroylation

Doi:10.1016/j.tet.2018.03.048
(2018)
Doi:10.1021/ja01159a040
(1950)
An enantioselective route to trans-2,6-disubstituted piperidines

Doi:10.1016/S0040-4020(97)00377-3
(1997)
Montmorillonite clay catalyzed tosylation of alcohols and selective monotosylation of diols with p-toluenesulfonic acid: An enviro-economic route

Doi:10.1016/S0040-4020(00)00626-8
(2000)

Article Doi