RHODIUM(I) AND PLATINUM(II) COMPLEXES WITH CHELATING BIDENTATE ISONITRILE LIGANDS

DOI: 10.1016/S0022-328X(00)99439-7

Source and publish data:

Journal of Organometallic Chemistry p. 415 - 428 (1983)

Update date:2022-08-03

Topics:

Authors:

Winzenburg, Mark L.

Kargol, Joseph A.

Angelici, Robert J.

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

Article abstract of DOI:10.1016/S0022-328X(00)99439-7

Rhodium(I) complexes, A, where A^- = Cl^-, BF4^-, or BPh4^-, and A, where A^- = Cl^-, BPh4^-, or PF6^-, were prepared by reaction of 2 wit

Full text of DOI:10.1016/S0022-328X(00)99439-7

Products guided by the article

Product name:[Rh((CNC₆H₄OCH₂)2)2]⁽¹⁺⁾*B(C₆H₅)4^(1-)=[Rh((CNC₆H₄OCH₂)2)2]B(C₆H₅)4

Cas No:86500-92-7

R&D Labs maybe for 86500-92-7

Lyan Limited

Contact:86-021-52418058

Address:8/F, Building 6, Guiping Road No.333, Shanghai, 200233, China
Shanghai Maxchemco Chemical Industry Co., Ltd.

Contact:(86)21-51079223

Address:No.1305-8, B241, the Ecust Park, Huajing Road, Xuhui District, Shanghai
Wuhan Hanye Chemical New Material Co.,Ltd

Contact:+86-27-85308141

Address:LiuDian, Panlongcheng Economic Development Zone, HuangPi district, Wuhan, Hubei 430311 P.R.China
Jinan Jinguilin Chemical Co.,Ltd

Contact:+86-531-81188412

Address:3rd floor of Torch Building, Huanyuan Rd, City of Jinan
Feis International Trade Co,. Ltd

Contact:13961823444-18235944442

Address:Wuxi jiangsu

Relevant to this article

Optimization of piperazinebenzylamines with a N-(1-methoxy-2-propyl) side chain as potent and selective antagonists of the human melanocortin-4 receptor

Doi:10.1016/j.bmcl.2005.06.058
(2005)
A Convenient Synthesis of Vinyl Triflates from Enones

Doi:10.1055/s-1985-31204
(1985)
Synthesis of 1α-Hydroxyvitamin D₅ using a modified two wavelength photolysis for vitamin D formation

Doi:10.1021/jo050853f
(2005)
Design, synthesis and biological evaluation of new β-carboline-bisindole compounds as DNA binding, photocleavage agents and topoisomerase I inhibitors

Doi:10.1016/j.ejmech.2017.10.054
(2018)
Improved Total Synthesis of Tubulysins and Design, Synthesis, and Biological Evaluation of New Tubulysins with Highly Potent Cytotoxicities against Cancer Cells as Potential Payloads for Antibody-Drug Conjugates

Doi:10.1021/jacs.7b12692
(2018)
Orally bioavailable prodrugs of a BCS class 2 molecule, an inhibitor of HIV-1 reverse transcriptase

Doi:10.1016/j.bmcl.2008.10.090
(2008)

Article Doi