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Volumn 49, Issue 3, 2010, Pages 545-547

Modeling of the 5′-deiodination of thyroxine by iodothyronine deiodinase: Chemical corroboration of a selenenyl iodide intermediate

Author keywords

Enzyme models; Iodine; Reactive intermediates; Selenium; Steric hindrance

Indexed keywords

CATALYTIC CYCLES; CHEMICAL PROCESS; DEIODINATION; ENZYME MODELS; IODOTHYRONINE; MOLECULAR CAVITY; REACTIVE INTERMEDIATE; REACTIVE INTERMEDIATES; STERIC HINDRANCES;

EID: 74549131806     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.200905796     Document Type: Article
Times cited : (55)

References (42)
  • 14
    • 0035796663 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 2486-2489;
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 2486-2489
  • 34
    • 0348134873 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 5714-5717;
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 5714-5717
  • 40
    • 0003517974 scopus 로고    scopus 로고
    • note
    • 2 using SHELXL 97 (G. M. Sheldrick, Program for Crystal Structure Refinement, University of Göttingen, 1997). The non-hydrogen atoms were refined anisotropically. The hydrogen atoms were idealized by using the riding models. CCDC 750141 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc. cam.ac.uk/data-request/cif.
    • (1997) Program for Crystal Structure Refinement
    • Sheldrick, G.M.1
  • 42
    • 74549182150 scopus 로고    scopus 로고
    • [3c] It was found that the reaction of 2 with monothiols proceeds readily to afford the corresponding selenenyl sulfides (ArSeSR) although further reduction to the selenol is very slow
    • [3c] It was found that the reaction of 2 with monothiols proceeds readily to afford the corresponding selenenyl sulfides (ArSeSR) although further reduction to the selenol is very slow.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.