METATHESIS OF DIALKENYLSILANES AND POLYMERIZATION OF 1,1-DIMETHYL-1-SILA-3-CYCLOPENTENE IN PRESENCE OF ALUMINIUM-RHENIUM CATALYSTS

DOI: 10.1007/BF00949601

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 483 - 487 (1981)

Update date:2022-08-04

Topics:

Authors:

Finkel'shtein, E. Sh.

Portnykh, E. B.

Ushakov, N. V.

Vdovin, V. M.

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

Article abstract of DOI:10.1007/BF00949601

Full text of DOI:10.1007/BF00949601

Products guided by the article

Product name:4,9-disila-4,4,9,9-tetramethyl-1,6,11-dodecatriene

Cas No:78558-53-9

R&D Labs maybe for 78558-53-9

Changsha Nutritopper Bio Technology Co.,Ltd.

Contact:+86-731-87803543

Address:East 1st Street, Baima Road, Ningxiang County
Hubei Vanz Pharm Co.,Ltd

website:http://www.vanzpharm.com/en/index.html

Contact:86-27-84492310

Address:FANHU INDUSTRY PARK
KA-SHING Business Trade Macau Co., Ltd.

Contact:00853-28430045

Address:23rd Floor, Block 3 La Cite, Areia Preta, Macao
Tianjin Bright Future Technology Co., Ltd

Contact:0086-22-58016666

Address:NO.136 DongTeng Lake Street Tianjin Economic and Technology Development Area,Tainjin,China
Second Pharma Co., Ltd

Contact:+86-575-82733999 0575-82732999

Address:hangzhou gulf fine chemical zone,shangyu city,zhejiang province

Relevant to this article

Asymmetric Copper-Catalyzed Intermolecular Aminoarylation of Styrenes: Efficient Access to Optical 2,2-Diarylethylamines

Doi:10.1021/jacs.7b02455
(2017)
Doi:10.1093/geront/41.2.210
(1941)
Oxochromium(IV) porphyrins and their relationship to heme proteins

Doi:10.1021/ic00132a078
(1982)
TOTAL SYNTHESIS OF CURZERENONE AND EPICURZERENONE

Doi:10.1246/cl.1981.593
(1981)
Stereoselective Alkylation and Aldol Reactions of (S)-(-)-β-Hydroxy-γ-butyrolactone Dianion

Doi:10.1021/jo00334a054
(1981)
Synthesis, preliminarily biological evaluation and molecular docking study of new Olaparib analogues as multifunctional PARP-1 and cholinesterase inhibitors

Doi:10.1080/14756366.2018.1530224
(2019)

Article Doi