2004
DOI: 10.1039/b404305g
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N-Salicylideneamino acidato complexes of oxovanadium(iv). The cysteine and penicillamine complexes

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Cited by 26 publications
(10 citation statements)
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“…These properties for the vanadium complexes are applied to many scientific fields, for example, catalytic chemistry [2], bioinorganic chemistry [3], electrochemistry [4,5] and molecule-based magnetism [6][7][8][9][10][11][12][13][14]. There are numbers of papers for the tetravalent vanadium complexes which have strong vanadium-oxygen multiple covalent bonds [15,16].…”
Section: Introductionmentioning
confidence: 97%
“…These properties for the vanadium complexes are applied to many scientific fields, for example, catalytic chemistry [2], bioinorganic chemistry [3], electrochemistry [4,5] and molecule-based magnetism [6][7][8][9][10][11][12][13][14]. There are numbers of papers for the tetravalent vanadium complexes which have strong vanadium-oxygen multiple covalent bonds [15,16].…”
Section: Introductionmentioning
confidence: 97%
“…Similar to complex 1, positive bands at 228 and 253 nm and negative bands at 211 and 278 nm were observed for complex 2, except a negative band at 240 nm. 37 Further, the relative intensities of these bands are different between complex 1 and 2. The difference in the CD spectrum could be attributed to the difference in the structure of complexes 1 and 2.…”
Section: Uv-visible and CD Spectramentioning
confidence: 97%
“…Aldol-type condensations have been carried out in the presence of vanadium (27), as well as Michael-type base-catalyzed additions (28) and asymmetric hetero Diels-Alder reactions (29). Several other vanadium mediated C-C bond formation reactions have also been reported (30), e.g., oxidative coupling of phenols, naphthols and arenes, asymmetric synthesis of BINOLs, Mannich-type (37) and modified Mannich-type reactions.…”
Section: Catalysismentioning
confidence: 99%
“…catalysis, insulin-enhancing, anti-tumor) of already known compounds. For example: Schiff bases of the salen-type (66), reduced Schiff bases of salan-type (171,172,173), sal-amino acidate and other Schiff bases, including the reducedtype derivatives, (28,78,193,195,197,216,217), amino acids or peptides (186)(187)(188)(189)196), hydroxycarboxylates (198,218,219,221) 158,180,184,[224][225][226][227][228][229][230][231][232][233][234].…”
Section: Coordination Chemistrymentioning
confidence: 99%
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