Scholarly article on niobium trichloride 13569-59-0 from Journal of the American Chemical Society p. 3690 - 3691

DOI: 10.1021/ja01134a504

Source and publish data:

Journal of the American Chemical Society p. 3690 - 3691 (1952)

Update date:2022-08-11

Topics:

Authors:

Brubaker, C. H.

Young, R. C.

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

Article abstract of DOI:10.1021/ja01134a504

Full text of DOI:10.1021/ja01134a504

Products guided by the article

Product name:niobium trichloride

Cas No:13569-59-0

R&D Labs maybe for 13569-59-0

Jintan Jinnuo Chemical Co., Ltd.

Contact:+86-519-80199901

Address:Room 1804, Building 1, Huacheng Business Plaza, Jintan, Jiangsu, China
Jinan Jianfeng Chemical Co., Ltd

Contact:0086-531-88110457

Address:sales01(-a-t-)pharmachemm{dot}c+o+m
WENZHOU M&C FOREIGN TRADE CO.,LTD.

Contact:+86-577-88862917

Address:No.8 Liming West Road,Wenzhou,zhejiang,China
SHANGHAI T&W PHARMACEUTICAL CO., LTD.

website:http://www.trustwe.com

Contact:+86-21-61551413

Address:601, No. 1, 2277 Nong, Zu Chongzhi Road, Zhangjiang Hightech. Park, Pudong
Foreschem Co., Ltd

Contact:+86-533-3112891

Address:zibo

Relevant to this article

Light-induced carboxylation of aryl derivatives with cooperative COF as an active photocatalyst and Ni(ii) co-catalyst

Doi:10.1039/d0nj05843b
(2021)
Samarium-induced iodine-catalyzed reduction of imines: Synthesis of amine derivatives

Doi:10.1016/S0040-4039(99)01395-7
(1999)
Doi:10.1039/jr9460000745
(1946)
Cooperation of the Neutral and the Cationic Leaving Group Pathways in Acid-Catalyzed O-Benzylation of TriBOT

Doi:10.1021/acs.joc.8b01505
(2018)
Highly efficient and chemoselective zinc-catalyzed hydrosilylation of esters under mild conditions

Doi:10.1002/chem.201406176
(2015)
Stereospecificity of the Hydride Transfer Reaction Catalyzed by Isopropylmalate Dehydrogenase of Thermophilic Bacteria Thermus thermophilius

Doi:10.1246/cl.1987.1749
(1987)

Article Doi

DOI: 10.1021/ja01134a504