Improved preparation of diaryl ditellurides

DOI: 10.1016/0022-328X(90)85348-3

Source and publish data:

Journal of Organometallic Chemistry p. 71 - 74 (1990)

Update date:2022-08-05

Topics:

Authors:

Engman, Lars

Persson, Joachim

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

Article abstract of DOI:10.1016/0022-328X(90)85348-3

Diaryl ditellurides have been synthesized from aryl bromides via lithiation, tellurium insertion, and ferricyanide oxidation of the resulting lithium arenetellurolates.

Full text of DOI:10.1016/0022-328X(90)85348-3

Products guided by the article

Product name:Benzene, 1,1'-ditellurobis[4-(trifluoromethyl)-

Cas No:129083-39-2

R&D Labs maybe for 129083-39-2

Chemsky（shanghai）International Co.,Ltd.

Contact:0

Address:0
RongCheng K&S Chemical Co.,Ltd

Contact:0631-7336369

Address:rongcheng ,shandong province china
Onlychem (Jinan)Biotech Co.,Ltd

Contact:86-531-83175885

Address:No. 44, Honglou South Road, Jinan,China
Tianjin Emulsion Science&Technology Development Co.,Ltd

Contact:13901380442

Address:Vake Garden New Town New Yi Bai Road Beichen District Tianjin,China
Rayfull Holding Co., Ltd

Contact:+86-577-65618087-605

Address:Room 402, Unit 4 Xinhu Bldg. Waitan Ruian City, Zhejiang China.

Relevant to this article

1H NMR Analyses, Shielding Mechanisms, Coupling Constants, and Comformations is Steroids Bearing Halogen, Hydroxy, Oxo Groups, and Double Bonds

Doi:10.1021/ja00310a046
(1985)
Doi:10.1007/BF00925630
()
NiH-Catalyzed Hydroamination/Cyclization Cascade: Rapid Access to Quinolines

Doi:10.1021/acscatal.1c02055
(2021)
Doi:10.1002/jps.2600650106
(1976)
Doi:10.1016/S0022-328X(00)91973-9
(1976)
Structure-based design and synthesis of potent benzothiazole inhibitors of interleukin-2 inducible T cell kinase (ITK)

Doi:10.1016/j.bmcl.2013.09.069
(2013)

Article Doi