Scholarly article on 1-(Ge(C2H5)3)-2-(C6H5)-1.2-C2B10H10 26201-01-4 from Journal of Organometallic Chemistry p. 211 - 216

DOI: 10.1016/S0022-328X(00)94161-5

Source and publish data:

Journal of Organometallic Chemistry p. 211 - 216 (1965)

Update date:2022-08-03

Topics:

Authors:

Zakharin, L. I.

Bregadze, V. I.

Okhlobystin, O. Yu.

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

Article abstract of DOI:10.1016/S0022-328X(00)94161-5

Full text of DOI:10.1016/S0022-328X(00)94161-5

Products guided by the article

Product name:1-(Ge(C₂H₅)3)-2-(C₆H₅)-1.2-C₂B₁₀H₁₀

Cas No:26201-01-4

R&D Labs maybe for 26201-01-4

Shanghai Harvest Chemical Ind. Co., Ltd.

Contact:021-51385350

Address:ROOM 806-807, AI LI CHEN BUILDING, No.333 JINGXIANG ROAD, PUDONG DISTRICT, 201206, SHANGHAI
Chengdu Yunyi International Trade Co., Ltd

Contact:

Address:china
uni source industries limited

Contact:86 21 3772 9386

Address:Rm.1803,Starry Bldg.1,1505 Meijiabang Road,Shanghai 201620 China
Chengdu Shengnuo Biological Technology Co., Ltd.

Contact:86-028-85275045

Address:Sichuan Province Chengdu hi tech Zone Tianfu Avenue North of 1480
Zibo Linzi Darong Fine Chemical Co., Ltd(expird)

Contact:86-532-67773200; 15689126900

Address:Qidu town,Linzi district,Zibo city,Shandong province,China

Relevant to this article

Radical-mediated furanose ring reconstruction from 2′,3′-seco-uridine

Doi:10.1016/S0040-4020(01)00203-4
(2001)
Diastereoselective Baylis-Hillman reactions: The design and synthesis of a novel camphor-Based chiral auxiliary

Doi:10.1021/ol990315n
(2000)
Deeper Insight into the Six-Step Domino Reaction of Aldehydes with Malononitrile and Evaluation of Antiviral and Antimalarial Activities of the Obtained Bicyclic Products

Doi:10.1002/open.201700005
(2017)
Sulfur-containing mixed-donor tribenzo-macrocycles and their endo-and exocyclic supramolecular silver(I) and copper(I) complexes

Doi:10.1021/ic1007473
(2010)
Homologation of allylic alcohols. An approach to cyclic and acyclic polyoxygenated compounds

Doi:10.1016/S0040-4039(99)02263-7
(2000)
A Bioorthogonal Click Chemistry Toolbox for Targeted Synthesis of Branched and Well-Defined Protein–Protein Conjugates

Doi:10.1002/anie.201915079
(2020)

Article Doi

DOI: 10.1016/S0022-328X(00)94161-5