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Volumn 6, Issue 7, 2000, Pages 1193-1198

Catalysis of the addition of benzenethiol to 2-cyclohexen-1-ones by uranyl-salophen complexes: A catalytic metallocleft with high substrate specificity

Author keywords

Enzyme mimetics; Kinetics; Michael additions; Substrate specificity; Supramolecular metallocatalysts

Indexed keywords

2 CYCLOHEXENONE; ACETAMINOSALOL; ANTINEMATODAL AGENT; CYCLOHEXANONE DERIVATIVE; ENZYME; ORGANOMETALLIC COMPOUND; PHENOL DERIVATIVE; SALICYLIC ACID DERIVATIVE; THIOL DERIVATIVE; THIOPHENOL; URANIUM; URANYL ACETATE;

EID: 0034599365     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3765(20000403)6:7<1193::AID-CHEM1193>3.3.CO;2-6     Document Type: Article
Times cited : (32)

References (24)
  • 3
    • 0000279988 scopus 로고
    • c) A. J. Kirby, Angew. Chem. 1995, 108, 770-790; Angew. Chem. Int. Ed. Engl. 1996, 35, 707-724;
    • (1995) Angew. Chem. , vol.108 , pp. 770-790
    • Kirby, A.J.1
  • 4
    • 33746204093 scopus 로고    scopus 로고
    • c) A. J. Kirby, Angew. Chem. 1995, 108, 770-790; Angew. Chem. Int. Ed. Engl. 1996, 35, 707-724;
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 707-724
  • 6
    • 0000227582 scopus 로고    scopus 로고
    • (Eds.: J. L. Atwood, J. E. D. Davies, D. D. MacNicol, F. Vögtle), Pergamon, Oxford
    • e) M.C. Feiters in Comprehensive Supramolecular Chemistry, Vol. 10 (Eds.: J. L. Atwood, J. E. D. Davies, D. D. MacNicol, F. Vögtle), Pergamon, Oxford, 1996, pp. 267-514;
    • (1996) Comprehensive Supramolecular Chemistry , vol.10 , pp. 267-514
    • Feiters, M.C.1
  • 14
    • 85050272509 scopus 로고
    • (Ed.: E. L. Eliel, S. H. Wilen, N. L. Allinger), Wiley, New York
    • a) H. Wynberg, in Topics in Stereochemistry, Vol. 16 (Ed.: E. L. Eliel, S. H. Wilen, N. L. Allinger), Wiley, New York, 1986, pp. 87-129;
    • (1986) Topics in Stereochemistry , vol.16 , pp. 87-129
    • Wynberg, H.1
  • 19
    • 5544253003 scopus 로고    scopus 로고
    • note
    • From the data in Table 2 it is easily calculated that 2 picks out and delivers to benzenethiol one molecule of 3a mixed with 99 molecules of 6a with a probability of 99.7%. The small (ca. 2%) calculated yield of 6b in the final reaction mixture is almost exclusively due to the competing background reaction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.