Results 121 to 130 of about 51,297 (183)

Research progress of ginseng active ingredients combined with chemotherapy in cancer therapy. [PDF]

J Ginseng Res
Zhang Y, Shao C, Li J, Bai Y, Li G, Ren T.   +5 more
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Chiral benzo[2.2.1] α-hydroxyketones from a dirhodium(ii)/bisphosphine-catalyzed desymmetrization addition reaction. [PDF]

Chem Sci
Zhan S, Wang C, Duan L, Gu Z.
europepmc   +1 more source

Sodium phosphaethynolate as P-source for the synthesis of molecular rhodium phosphides: an exploratory study.

Dalton Trans
Li Z, Borger JE, Gianetti TL, Müller F, Pribanic B, Coburger P, Grützmacher H.   +6 more
europepmc   +1 more source

Enantioselective intramolecular cyclopropanation via a cationic sulfoxonium-Rh-carbene. [PDF]

Nat Commun
Xing Y, Fang Y, Shiri F, Lin Z, Chen J, Wang Z, Huang Y.   +6 more
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Rhodium-catalysed connective synthesis of diverse reactive probes bearing S(VI) electrophilic warheads. [PDF]

Beilstein J Org Chem
Rice S, Chesti J, Mosedale WRT, Wright MH, Marsden SP, Smith TK, Nelson A.   +6 more
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Targeting Autophagy in Ovarian Cancer: The Emerging Role of Ginsenosides. [PDF]

Cancer Med
Guo Y, Yun C, Zhang Y, Yang X, Liu H.
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CO on a Rh/Fe₃O₄ single-atom catalyst: high-resolution infrared spectroscopy and near-ambient-pressure scanning tunnelling microscopy.

Faraday Discuss
Barama NEH, Wang C, Sombut P, Rath D, Lagin A, Ormoš M, Puntscher L, Lewis FJ, Jakub Z, Kraushofer F, Eder M, Meier M, Schmid M, Diebold U, Franchini C, Matvija P, Pavelec J, Parkinson GS.   +17 more
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Anticancer Effects of Ginsenoside Rh2: A Systematic Review

Current Molecular Pharmacology, 2021
Background: As one of the effective pharmacological constituents of Ginseng Radix et Rhizoma, ginsenoside Rh2 (Rh2) exerts a remarkable anticancer effect on various cancer cell lines in vitro and strongly inhibits tumor growth in vivo without severe toxicity. Objective: This article reviewed existing evidence supporting the anticancer effects of Rh2
Xin-Ling, He, Xiao-Huang, Xu, Jia-Jie, Shi, Mingqing, Huang, Yitao, Wang, Xiuping, Chen, Jin-Jian, Lu   +6 more
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Asymmetric, redox-active carbonyl complexes with [Rh2]2+, [Rh2]3+, and [Rh2]4+ cores

Journal of the Chemical Society, Chemical Communications, 1987
The [Rh2]2+ complex [Rh2(CO)2(bipy)(µ-RNNNR)2](2, bipy = 2,2′-bipyridyl, R =p-tolyl) is the precursor to asymmetric, redox-active [Rh2]3+ and [Rh2]4+ derivatives such as [Rh2(CO)L(bipy)(µ-RNNNR)2]z(3+, L = PPh3, z= 1; 4, L = I, z= 0) and [Rh2(CO)(S2CNMe2)(piby)(µ-RNNNR)2][PF6](5) respectively.
Neil G. Connelly, Gabriel Garcia
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