Scholarly article on trimethylgermyl trifluoromethane sulfonate 41524-05-4 from Journal of Inorganic and Nuclear Chemistry p. 1473 - 1478

DOI: 10.1016/0022-1902(81)80319-3

Source and publish data:

Journal of Inorganic and Nuclear Chemistry p. 1473 - 1478 (1981)

Update date:2022-08-03

Topics:

Authors:

Drake, John E.

Khasrou, Layla N.

Majid, Abdul

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

Article abstract of DOI:10.1016/0022-1902(81)80319-3

Full text of DOI:10.1016/0022-1902(81)80319-3

Products guided by the article

Product name:trimethylgermyl trifluoromethane sulfonate

Cas No:41524-05-4

R&D Labs maybe for 41524-05-4

Henan Yellow River New Material Technology Co.Ltd.

website:http://www.yellowriverchem.com

Contact:0086-373-7278760

Address:Chengguan Town, Yuanyang County
Ring Specialty Chemicals Inc.

website:http://www.ringchemicals.com/

Contact:+1-416-493-6870

Address:Toronto, Canada
Zhenjiang Huayu I/E Co.,LTD

Contact:86-511-85210668 0511-85210668, 85210818, 85210898

Address:Yihai Garden E-902,NO.99 Daxi RD., Zhenjiang Jiiangsu ,China
SHANGHAI GILEADER ADVANCE MATERIAL TECHNOLOGY CO.,LTD

website:http://www.tanguitech.com/contact.asp

Contact:+86-021-58692556

Address:No.6 Building,No. 668 Hengan RD Pudong,Shanghai
He Bei Shun Er Chemical Co., LTD.

Contact:86-0311-86996932/86860168

Address:No 18,North street

Relevant to this article

Doi:10.1007/BF00480564
()
Resistance-modifying agents. Part 7: 2,6-Disubstituted-4,8-dibenzylaminopyrimido[5,4-d]pyrimidines that inhibit nucleoside transport in the presence of α₁-acid glycoprotein (AGP)

Doi:10.1016/S0960-894X(00)00053-6
(2000)
Lewis acid/Broensted acid mediated benz-annulation of thiophenes and electron-rich arenes

Doi:10.1021/ol501006t
(2014)
Tunable stereoselective hydrosilylation of PhC≡CH catalyzed by Cp*Rh complexes

Doi:10.1021/om010978k
(2002)
Rearrangement of ammonium ylides produced by intramolecular reaction of catalytically generated metal carbenoids. Part 2. Stereoselective synthesis of bicyclic amines

Doi:10.1039/b108182a
(2001)
Controlled stepwise conversion of 2,4,6,8-tetrachloropyrimido[5,4-d]pyrimidine into 2,4,6,8-tetrasubstituted pyrimido[5,4-d]pyrimidines

Doi:10.1039/b102224p
(2002)

Article Doi

DOI: 10.1016/0022-1902(81)80319-3