Scholarly article on trans-Rh(PPh(o-C6H4CH3)2)2Cl2 29632-34-6 from Journal of the American Chemical Society p. 6266,6269,6274,6279

DOI: 10.1021/ja01051a014

Source and publish data:

Journal of the American Chemical Society p. 6266,6269,6274,6279 (1969)

Update date:2022-08-05

Topics:

Authors:

Bennett Bennett

Longstaff

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

Article abstract of DOI:10.1021/ja01051a014

Full text of DOI:10.1021/ja01051a014

Products guided by the article

Product name:trans-Rh(PPh(o-C₆H₄CH₃)2)2Cl₂

Cas No:29632-34-6

R&D Labs maybe for 29632-34-6

Xi'an caijing Opto-Electrical Science & Technology Co., LTD

Contact:+86-29-88294447

Address:NO.168 Zhangba Rd. East, Xi'an, P.R.China
Weihao Chemtech (ChangZhou) Co., Ltd.(expird)

Contact:051989185693

Address:NO 217 huangshan Rd ,Changzhou
Oceachem Group Limited

website:http://www.oceanchem-group.com

Contact:86-536-8596048

Address:9th floor,Building B future Plaza, No.88.Fenghuang Street,Weifang,Shandong,China
Shandong Bolode Bio-Technology Co., LTD

Contact:+86-0531-58966870

Address:136 Jingyi Road,Huaiyin District,Jinan,Shandong,China
Jiangxi Dongbang Pharmaceutical Co., Ltd.

Contact:+86-795-4433603, 4433388

Address:Fengxin Industrial Park, Fengxin County, Jiangxi Province, P.R.C

Relevant to this article

Regioncontrol by the carbon-carbon double bond in the Rh₂(OAc)₄ mediated carbon-hydrogen insertion of α-diazo-ketones

Doi:10.1016/S0040-4020(01)89741-6
(1991)
Preparation of 2-BF₃-substituted 1,3-dienes and their Diels-Alder/cross-coupling reactions

Doi:10.1021/ol050794s
(2005)
32. Biosynthetic production of [N²,1,3,7,9-¹⁵N]guanosine and [1,3,7,9-¹⁵N]inosine and conversion into [N⁶,1,3,7,9-¹⁵N]adenosine for structure elucidation of RNA by heteronuclear NMR

Doi:10.1002/hlca.19950780213
(1995)
Alkyl migration reactions - The direct observation of the preferential migration of branched over linear alkyl groups

Doi:10.1016/S0022-328X(00)00158-3
(2000)
Synthesis of novel substituted 2-lactosylthiothieno[2,3-d]pyrimidin-4(3H)-one derivatives

Doi:10.1002/jhet.1794
(2015)
Enantioselective synthesis of spiro[4H-pyran-3,3′-oxindole] derivatives catalyzed by cinchona alkaloid thioureas: Significant water effects on the enantioselectivity

Doi:10.1080/00397911.2019.1651866
(2019)

Article Doi

DOI: 10.1021/ja01051a014