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Volumn 13, Issue 23, 2007, Pages 6674-6681

Comparative study of metal-catalyzed iminations of sulfoxides and sulfides

Author keywords

Homogeneous catalysis; Iminations; Sulfilimines; Sulfoximines; Sulfur

Indexed keywords

CATALYST ACTIVITY; PARAFFINS; REDOX REACTIONS; SUBSTITUTION REACTIONS;

EID: 34547755047     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200700352     Document Type: Article
Times cited : (68)

References (84)
  • 1
    • 0034835354 scopus 로고    scopus 로고
    • For selected examples, see: a
    • For selected examples, see: a) C. Bolm, O. Simic, J. Am. Chem. Soc. 2001, 123, 3830-3831;
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 3830-3831
    • Bolm, C.1    Simic, O.2
  • 7
    • 9244221087 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 5984-5987;
    • (2004) Chem. Int. Ed , vol.43 , pp. 5984-5987
    • Angew1
  • 9
    • 28244467432 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 7564-7567;
    • (2005) Chem. Int. Ed , vol.44 , pp. 7564-7567
    • Angew1
  • 13
  • 21
    • 34547816578 scopus 로고    scopus 로고
    • Methoden Org. Chem. (Houben-Weyl), E11 (Ed.: D. Klamann), Thieme, Stuttgart, 1985, Parts 1-2;
    • b) Methoden Org. Chem. (Houben-Weyl), Vol. E11 (Ed.: D. Klamann), Thieme, Stuttgart, 1985, Parts 1-2;
  • 22
    • 0003047995 scopus 로고
    • c) S. Pyne, Sulfur Rep. 1992, 72, 57-89;
    • (1992) Sulfur Rep , vol.72 , pp. 57-89
    • Pyne, S.1
  • 29
  • 33
    • 34547778893 scopus 로고    scopus 로고
    • M. Fieser, L. F. Fieser, Reagents for Organic Synthesis, 5, Wiley, New York, 1975, p. 430; see also:
    • d) M. Fieser, L. F. Fieser, Reagents for Organic Synthesis, Vol. 5, Wiley, New York, 1975, p. 430; see also:
  • 35
    • 26844488178 scopus 로고    scopus 로고
    • For alternative metal-free sulfoxide iminations, see: a
    • For alternative metal-free sulfoxide iminations, see: a) G. Y. Cho, C. Bolm, Tetrahedron Lett. 2005, 46, 8007-8008,
    • (2005) Tetrahedron Lett , vol.46 , pp. 8007-8008
    • Cho, G.Y.1    Bolm, C.2
  • 39
    • 33947335102 scopus 로고
    • For the first reported copper-catalyzed imination of sulfoxides, see
    • For the first reported copper-catalyzed imination of sulfoxides, see : H. Kwart, A. A. Kahn, J. Am. Chem. Soc. 1967, 89, 1950-1951.
    • (1967) J. Am. Chem. Soc , vol.89 , pp. 1950-1951
    • Kwart, H.1    Kahn, A.A.2
  • 47
    • 34547764781 scopus 로고    scopus 로고
    • for other example of Cu-catalyzed iminations, see: H. Takada, K. Ohe, S. Uemura, Angew. Chem. 1999, 111, 1367-1369;
    • b) for other example of Cu-catalyzed iminations, see: H. Takada, K. Ohe, S. Uemura, Angew. Chem. 1999, 111, 1367-1369;
  • 48
    • 0033519191 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 1288-1289.
    • (1999) Chem. Int. Ed , vol.38 , pp. 1288-1289
    • Angew1
  • 50
    • 34547803670 scopus 로고    scopus 로고
    • Despite the high reagent cost, the rhodium-catalyzed sulfoxide imination protocol has already been mentioned in the patent literature;
    • Despite the high reagent cost, the rhodium-catalyzed sulfoxide imination protocol has already been mentioned in the patent literature;
  • 54
    • 34547817619 scopus 로고    scopus 로고
    • EP 1710246 A1, 2006 Schering
    • d) U. Lucking, EP 1710246 A1, 2006 (Schering).
    • Lucking, U.1
  • 63
    • 0141485295 scopus 로고    scopus 로고
    • T. Uchida, Y. Tamura, M. Ohba, T. Katsuki, Tetrahedron Lett. 2003, 44, 7965-7968; see also:
    • g) T. Uchida, Y. Tamura, M. Ohba, T. Katsuki, Tetrahedron Lett. 2003, 44, 7965-7968; see also:
  • 64
    • 29344457003 scopus 로고    scopus 로고
    • h) T. Katsuki, Chem. Lett. 2005, 34, 1304-1309.
    • (2005) Chem. Lett , vol.34 , pp. 1304-1309
    • Katsuki, T.1
  • 65
    • 33846157174 scopus 로고    scopus 로고
    • For the use of the lability of sulfilimines to generate alkenes, see
    • For the use of the lability of sulfilimines to generate alkenes, see: J. Matsuo, T. Kozai, H. Ishibashi, Org. Lett. 2006, 8, 6095-6098.
    • (2006) Org. Lett , vol.8 , pp. 6095-6098
    • Matsuo, J.1    Kozai, T.2    Ishibashi, H.3
  • 66
    • 0000067190 scopus 로고
    • For oxygen-transfer reactions to thianthrene 5-oxide, see: a
    • For oxygen-transfer reactions to thianthrene 5-oxide, see: a) W. Adam, W. Haas, G. Seiker, J. Am. Chem. Soc. 1984, 106, 5020-5022;
    • (1984) J. Am. Chem. Soc , vol.106 , pp. 5020-5022
    • Adam, W.1    Haas, W.2    Seiker, G.3
  • 77
    • 0007164066 scopus 로고
    • For iminations of thianthrene and derivatives, see, a
    • For iminations of thianthrene and derivatives, see : a) H. J. Shine, X. J. Silber, J. Am. Chem. Soc. 1972, 94, 1026-1027;
    • (1972) J. Am. Chem. Soc , vol.94 , pp. 1026-1027
    • Shine, H.J.1    Silber, X.J.2
  • 81
    • 34547751325 scopus 로고    scopus 로고
    • The relative cis or trans configuration of sulfilimines 12 was determined by comparison with the literature data, see ref. [21].
    • The relative cis or trans configuration of sulfilimines 12 was determined by comparison with the literature data, see ref. [21].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.