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Volumn 70, Issue 2, 2005, Pages 624-630

Di- and trinuclear Zn2+ complexes of calix[4]arene based ligands as catalysts of acyl and phosphoryl transfer reactions

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLATION; CATALYST ACTIVITY; CATALYSTS; COMPLEXATION; CONFORMATIONS; ESTERS; ISOMERS; RNA; ZINC COMPOUNDS;

EID: 12344300154     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0487350     Document Type: Article
Times cited : (51)

References (39)
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    • note
    • Excess catalyst minimizes product inhibition as well as complications arising from multiple binding of carboxylate to di- and trimetallic complexes.
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    • note
    • The X-ray crystal structure of a neutral pentacoordinate species analogous to 15 involving monodentate binding of two carboxylate ions was reported in ref 7b.
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    • The widely accepted bifunctional mechanism for metal-catalyzed hydrolysis (alcoholysis) involves combined nucleophile delivery to and Lewis acid activation of the ester carbonyl (see: Chin, J. Acc. Chem. Res. 1991, 24, 145-152; for a recent example see ref 11). When applied to complex 15 such a mechanism would require an unlikely hexacoordination for a BAMP complexed Zn center.
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    • note
    • 2+ centers in a pentacoordinate geometry.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.