Synthesis of bis(pentachlorophenyl)silanediol and related compounds. Crystal structure of diethoxybis(pentachlorophenyl)silane

DOI: 10.1016/0022-328X(92)83111-T

Source and publish data:

Journal of Organometallic Chemistry p. 163 - 171 (1992)

Update date:2022-09-26

Topics:

Authors:

Carilla, Jose

Fajari, Lluis

Julia, Luis

Riera, Juan

Lloveras, Joaquin

et al. et al.

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

Article abstract of DOI:10.1016/0022-328X(92)83111-T

Bis(pentachlorophenyl) silanediol (3) has been prepared by neutral hydrolysis of perchlorodiphenylsilane (2).Reduction of 2 with LiAlH4 gives bis(pentachlorophenyl)silane (4) which upon treatment with bromine gives dibromobis(pentachlorophenyl)silane (5)

Full text of DOI:10.1016/0022-328X(92)83111-T

Products guided by the article

Product name:Silane, diethoxybis(pentachlorophenyl)-

Cas No:139556-58-4

R&D Labs maybe for 139556-58-4

Angel Yeast Co., Ltd.

Contact:+86-717-6370352

Address:168 Chengdong Avenue, Yichang, Hubei 443003, P. R.China
Weifang Jahwa Chemical Co.,Ltd

Contact:0086-536-8897731,8897730

Address:No.5166 East Dongfeng Street,Weifang,Shandong,China
shijiazhuang baisheng chem co.; ltd

Contact:86-0311-80790826

Address:shijiazhuang hebei
Zha Yan

Contact:+86-13914766747

Address:Floors 21&22, Jin Cheng Tower, No. 216 Middle Longpan Road, Nanjing
Shaanxi King Stone Enterprise Company Limited

Contact:86-29-88353805,13609285751

Address:.209 Keji Road Hi-Tech industrial Develpment Zone .Xian China

Relevant to this article

The Broad Aryl Acid Specificity of the Amide Bond Synthetase McbA Suggests Potential for the Biocatalytic Synthesis of Amides

Doi:10.1002/anie.201804592
(2018)
Selective phosphorylation of diols with a Lewis acid catalyst

Doi:10.1016/j.tetlet.2014.05.047
(2014)
Oxidative aliphatic C-H fluorination with fluoride ion catalyzed by a manganese porphyrin

Doi:10.1126/science.1222327
(2012)
Silica-supported ceric ammonium nitrate (CAN): a simple, mild and solid-supported reagent for quickest oxidative aromatization of Hantzsch 1,4-dihydropyridines

Doi:10.1007/s11696-018-0666-5
(2019)
THE SYNTHESIS OF (1-FLUOROVINYL)TRIBUTYLTIN: A SYNTHETIC EQUIVALENT FOR THE 1-FLUOROETHENE ANION.

Doi:10.1016/S0040-4039(00)77057-2
(1994)
Synthesis, absorption and fluorescence properties of N-triazinyl derivatives of 2-aminoanthracene

Doi:10.1016/j.dyepig.2011.08.018
(2012)

Article Doi