Scholarly article on Iodoborane 13842-56-3 from Journal of Molecular Spectroscopy p. 145 - 148

DOI: 10.1016/0022-2852(90)90284-W

Source and publish data:

Journal of Molecular Spectroscopy p. 145 - 148 (1990)

Update date:2022-07-28

Topics:

Authors:

Lebreton, J.

Ferran, J.

Mahieu, E.

Dubois, I.

Bredohl, H.

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

Article abstract of DOI:10.1016/0022-2852(90)90284-W

Full text of DOI:10.1016/0022-2852(90)90284-W

Products guided by the article

Product name:Iodoborane

Cas No:13842-56-3

R&D Labs maybe for 13842-56-3

Hubei Onward Bio-Development Co., Ltd.

Contact:+86-718-8417012

Address:No.517,Shizhou Avenue,Enshi City,Hubei Province,China,445002
taicang liyuan chemical co,.ltd

website:http://www.tcliyuanchem.com/productse.php

Contact:86-512-53539583

Address:Room 804,Huaxu Building,No.95,Renmin South Road,Taicang city,Jiangsu Province,China
Shandong Ailitong New Material Co.,Ltd

Contact:+86-536-3226266

Address:zhongjia village, putong town , qingzhou city,Shandong Province,China
Shanghai Micro-mega Industry Co., Ltd.

Contact:0086-21-34628682;57153848

Address:Rm413,No.413,West Meilong Road, Minhang District,Shanghai P R China
Rugao Jinling Chemical Co., Ltd.(expird)

Contact:0086-513-68005586

Address:Lianluo new village huangshi town Rugao city Jiangsu Province.

Relevant to this article

Ring transformations of β-lactam-condensed 1,3-benzothiazines to isoquinoline and thiazole derivatives by sulfur extrusion and addition sequences

Doi:10.1016/j.tet.2012.05.033
(2012)
Synthesis and evaluation of potent pyrrolidine H₃ antagonists

Doi:10.1016/S0960-894X(02)00685-6
(2002)
Doi:10.1016/0022-1902(68)80151-4
(1968)
Mechanisms of reactions of dihydrogen complexes: Formation of trans-[RuH(H₂)(dppe)₂]⁺ and substitution of coordinated dihydrogen

Doi:10.1021/ic9902267
(1999)
Doi:10.1021/jm00272a020
(1972)
Doi:10.1039/c39720000345
(1972)

Article Doi

DOI: 10.1016/0022-2852(90)90284-W