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Volumn , Issue 13, 2010, Pages 1919-1922

Enzymatic oxidative cyclisation reactions leading to dibenzoazocanes

Author keywords

Biotransformation; Enzymes; Heterocycles; Oxidation

Indexed keywords

AMINE; MONOPHENOL MONOOXYGENASE; TYRAMINE;

EID: 77955394945     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1258486     Document Type: Article
Times cited : (11)

References (41)
  • 10
    • 0003417469 scopus 로고
    • For example, see: Trost B. M. Fleming I. Pergamon Press Oxford
    • For example, see: Oxidation, In Comprehensive Organic Synthesis Vol. 7 Trost B M. Fleming I Pergamon Press Oxford 1991
    • (1991) Oxidation, in Comprehensive Organic Synthesis , vol.7
  • 25
    • 0028731907 scopus 로고
    • For reviews and recent prospects, see
    • For reviews and recent prospects, see:, Burton S G., Catal. Today 1994 22 459
    • (1994) Catal. Today , vol.22 , pp. 459
    • Burton, S.G.1
  • 39
    • 0026703223 scopus 로고
    • In one of the rotamers H-6a and the H-6b are, respectively, located at = 4.80 and 2.99 ppm are in an AB system with a coupling constant of 13.5 Hz. The high shift of H-6a is due to its position in the plane of the carbonyl. In the minor rotamer they are in the same system with a coupling constant of 14.5 Hz but at = 4.40 and 3.40 ppm, respectively. Moreover, COSY experiment showed that the protons H-9a and H-8b, and the H-9b and H-8a do not, respectively, couple because of their ca. 90 dihedral angle, thus confirming the TBC conformation. See also
    • In one of the rotamers H-6a and the H-6b are, respectively, located at = 4.80 and 2.99 ppm are in an AB system with a coupling constant of 13.5 Hz. The high shift of H-6a is due to its position in the plane of the carbonyl. In the minor rotamer they are in the same system with a coupling constant of 14.5 Hz but at = 4.40 and 3.40 ppm, respectively. Moreover, COSY experiment showed that the protons H-9a and H-8b, and the H-9b and H-8a do not, respectively, couple because of their ca. 90 dihedral angle, thus confirming the TBC conformation. See also:, Landais Y, Robin J, Tetrahedron 1992 48 7185
    • (1992) Tetrahedron , vol.48 , pp. 7185
    • Landais, Y.1    Robin, J.2
  • 40
    • 0030722720 scopus 로고    scopus 로고
    • Evidence of the indirect formation of the catecholic intermediate substrate responsible for the autoactivation kinetics of tyrosinase. See
    • Evidence of the indirect formation of the catecholic intermediate substrate responsible for the autoactivation kinetics of tyrosinase. See:, Cooksey C J., Garratt P J., Land E J., Pavel S, Ramsden C A., Riley P A., Smit N P. M., J. Biol. Chem. 1997 272 26226
    • (1997) J. Biol. Chem. , vol.272 , pp. 26226
    • Cooksey, C.J.1    Garratt, P.J.2    Land, E.J.3    Pavel, S.4    Ramsden, C.A.5    Riley, P.A.6    Smit, N.P.M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.