(trans-1R,2R-Cyclohexanediamine-N,N')(L-ascorbato-C2,O5)platinum(II)–Water (1/3)

Yuge, Hidetaka; Miyamoto, Takeshi

doi:10.1107/s0108270196009493

Cited by 4 publications

(3 citation statements)

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“…The reaction between cis -[Pt(OH) 2 (PMe 3 ) 2 ] and ascorbic acid afforded cis -[Pt(asc- O 2 , O 3 )(PMe 3 ) 2 ]·2H 2 O ( 157 ‘) as final product. The binding of the ascorbato ligand through O 2 and O 3 as in type 157 complexes was shown by X-ray crystallography 106a…”

Section: B Sugar Acid Ligandsmentioning

confidence: 99%

Carbohydrate Complexes of Platinum-Group Metals

2000

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Substituents 4298 III. Carbohydrate Ligands without Donor Groups 4299 A. Anionic Carbohydrate Ligands 4299 1. Carbohydrate Carbanions 4299 2. Carbohydrate Diolato Ligands 4300 B. Neutral Carbohydrate Ligands 4301 1. Platinum(IV) Complexes with Monoprotected Carbohydrate Ligands 4301 2. Platinum Complexes with Diprotected Carbohydrate Ligands 4303 3. Platinum Complexes with Glucopyranoside and Acetylated Carbohydrate Ligands 4304 4. Platinum Complexes with Nonprotected Carbohydrate Ligands 4304 5. Characterization of Carbohydrate Platinum(IV) Complexes 4305 IV. Sugar Alcohol and Sugar Acid Ligands 4305 A. Sugar Alcohol Ligands 4305 1. Sugar Alcohols without Donor Groups 4305 2. Sugar Alcohols with Donor Groups 4306 3. Diolato Ligands 4307 B. Sugar Acid Ligands 4309 V. Cyclodextrin Complexes 4311 A. Inclusion Compounds 4311 B. Cyclodextrins with Donor Groups 4313 VI. Conclusion 4314 VII. Abbrevations 4315 VIII. Acknowledgments 4315 IX. References 4315

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Section: B Sugar Acid Ligandsmentioning

confidence: 99%

Carbohydrate Complexes of Platinum-Group Metals

2000

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“…8 Similar complexes with the (cyclohexane-1,2-diamine)platinum( ii ) moiety and a C , O -chelating ligand have been reported only scarcely. These focus mainly on ascorbato complexes, 9–19 but are not limited thereto. 20,21 Furthermore, complexes with up to two coordinating nitrogen atoms and at least one coordinating carbon atom are known as well.…”

Section: Introductionmentioning

confidence: 99%

“…8 Similar complexes with the (cyclohexane-1,2-diamine)platinum(II) moiety and a C,O-chelating ligand have been reported only scarcely. These focus mainly on ascorbato complexes, [9][10][11][12][13][14][15][16][17][18][19] but are not limited thereto. 20,21 Scheme 1 Chemical structure of oxaliplatin.…”

Section: Introductionmentioning

confidence: 99%

Not the usual suspect – an unexpected organometallic product during the synthesis of cytotoxic platinum(ii) complexes

Maier,

Wutschitz,

Gajic

et al. 2023

Dalton Trans.

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Synthesis of Metal Enolato Complexes

Vicente

2010

Patai's Chemistry of Functional Groups

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Introduction Synthesis from Ketones, Aldehydes and Esters Synthesis from Ketenes, Isocyanates and Acyl Halides Synthesis from Carbon Monoxide and Carbonyl Complexes Synthesis via Cleavage of Ethers and Related Compounds Synthesis from Oxo, Hydroxo or Alkoxo Complexes Oxygenation Reactions Miscellaneous Reactions Acknowledgments

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(trans-1R,2R-Cyclohexanediamine-N,N')(L-ascorbato-C2,O5)platinum(II)–Water (1/3)

Cited by 4 publications

References 4 publications

Carbohydrate Complexes of Platinum-Group Metals

Carbohydrate Complexes of Platinum-Group Metals

Not the usual suspect – an unexpected organometallic product during the synthesis of cytotoxic platinum(ii) complexes

Synthesis of Metal Enolato Complexes

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