메뉴 건너뛰기




Volumn 37, Issue 25, 1972, Pages 4045-4060

Thiocarbonyl Ylides. Generation, Properties, and Reactions

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33947089660     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo00798a016     Document Type: Article
Times cited : (180)

References (105)
  • 3
    • 0001427691 scopus 로고
    • This name is based on the nomenclature suggested by
    • This name is based on the nomenclature suggested by R. Huisgen, Angew. Chem., 75, 604 (1963).
    • (1963) Angew. Chem. , vol.75 , pp. 604
    • Huisgen, R.1
  • 5
    • 33144470975 scopus 로고
    • See, for a theoretical discussion of the situation in thiophene
    • See, for a theoretical discussion of the situation in thiophene, M. J. Bielefeld and D. D. Fitts, Chern. Soc., 88, 4804 (1966).
    • (1966) Chern. Soc. , vol.88 , pp. 4804
    • Bielefeld, M.J.1    Fitts, D.D.2
  • 15
    • 85022409566 scopus 로고
    • G. Nickless, Ed., Elsevier, New York, N. Y.
    • H. G. Heal, “Inorganic Sulfur Chemistry,” G. Nickless, Ed., Elsevier, New York, N. Y., 1968, p 459.
    • (1968) Inorganic Sulfur Chemistry , pp. 459
    • Heal, H.G.1
  • 16
    • 0041192679 scopus 로고
    • For a 1,3-dipolar addition of 7, see
    • For a 1,3-dipolar addition of 7, see M. R. Brinkman and C. W. Allen, J. Amer. Chem. Soc., 94, 1550 (1972).
    • (1972) J. Amer. Chem. Soc. , vol.94 , pp. 1550
    • Brinkman, M.R.1    Allen, C.W.2
  • 20
    • 0009298978 scopus 로고
    • and references contained therein
    • G. Kresze and W. Wucherpfennig, Angew. Chem., 79, 109 (1967), and references contained therein.
    • (1967) Angew. Chem. , vol.79 , pp. 109
    • Kresze, G.1    Wucherpfennig, W.2
  • 21
    • 0004009372 scopus 로고
    • For a description, see Interscience, New York, N. Y.
    • For a description, see F. A. Cotton and E. Wilkinson, “Advanced Inorganic Chemistry,” Interscience, New York, N. Y., 1966, pp 534-540.
    • (1966) Advanced Inorganic Chemistry , pp. 534-540
    • Cotton, F.A.1    Wilkinson, E.2
  • 22
    • 33748968666 scopus 로고
    • For early studies on the addition of sulfur dioxide to dienes, see
    • For early studies on the addition of sulfur dioxide to dienes, see H. J. Backer, J. Strating, and C. M. H. Kool, Recl. Trav. Chim. Pays-Bas, 58, 778 (1939).
    • (1939) Recl. Trav. Chim. Pays-Bas , vol.58 , pp. 778
    • Backer, H.J.1    Strating, J.2    Kool, C.M.H.3
  • 23
    • 0003117406 scopus 로고
    • For an early MO description, see (a)
    • For an early MO description, see (a) H. P. Koch and W. E. Moffit, Trans. Faraday Soc., 47, 7 (1951);
    • (1951) Trans. Faraday Soc. , vol.47 , pp. 7
    • Koch, H.P.1    Moffit, W.E.2
  • 24
    • 0003438540 scopus 로고
    • also Cornell University Press, 3rd ed, Ithaca, N. Y.
    • also L. Pauling, “The Nature of the Chemical Bond,” Cornell University Press, 3rd ed, Ithaca, N. Y., 1960.
    • (1960) The Nature of the Chemical Bond
    • Pauling, L.1
  • 46
    • 37049119308 scopus 로고
    • The principle of olefin synthesis by a “twofold extrusion process” has been elegantly enunciated by
    • The principle of olefin synthesis by a “twofold extrusion process” has been elegantly enunciated by D. H. R. Barton and B. J. Willis, J. Chem. Soc., Perkin Trans. I, 305 (1972);
    • (1972) J. Chem. Soc., Perkin Trans. I , pp. 305
    • Barton, D.H.R.1    Willis, B.J.2
  • 47
    • 85022623777 scopus 로고
    • Among the compounds investigated was a thiadiazolidine (see further) that was concurrently prepared by our group.1 We are grateful to Professor Barton for correspondence on this matter
    • Chem. Commun., 1225 (1970), Among the compounds investigated was a thiadiazolidine (see further) that was concurrently prepared by our group.1 We are grateful to Professor Barton for correspondence on this matter.
    • (1970) Chem. Commun. , pp. 1225
  • 48
    • 0001833189 scopus 로고
    • See, for an early example
    • See, for an early example, E. B. Knott, J. Chem. Soc., 916 (1955).
    • (1955) J. Chem. Soc. , pp. 916
    • Knott, E.B.1
  • 63
    • 0001784199 scopus 로고
    • M. J. Janssen, Ed., Interscience, New York, N. Y.
    • R. Mayer, “Organosulfur Chemistry,” M. J. Janssen, Ed., Interscience, New York, N. Y., 1967, pp 219-240.
    • (1967) Organosulfur Chemistry , pp. 219-240
    • Mayer, R.1
  • 64
    • 33947290999 scopus 로고
    • reported the successful isolation of 1,3,4-thiadiazolines from the reactions of diazomethane with some spiro thioketones
    • A. P. Krapcho, D. R. Raa, M. P. silvon, and B. Abegaz, J. Org. Chem., 36, 3885 (1971), reported the successful isolation of 1,3,4-thiadiazolines from the reactions of diazomethane with some spiro thioketones.
    • (1971) J. Org. Chem. , vol.36 , pp. 3885
    • Krapcho, A.P.1    Raa, D.R.2    silvon, M.P.3    Abegaz, B.4
  • 89
    • 33947299307 scopus 로고
    • A “recoil” effect resulting in inversion of configuration at the carbon atom is suggested to be operative at least in bicyclic compounds
    • A “recoil” effect resulting in inversion of configuration at the carbon atom is suggested to be operative at least in bicyclic compounds: E. L. Allred and R. L. Smith, J. Amer. Chem. Soc., 91, 6766 (1969).
    • (1969) J. Amer. Chem. Soc. , vol.91 , pp. 6766
    • Allred, E.L.1    Smith, R.L.2
  • 90
    • 0001387888 scopus 로고
    • Strong conformational preferences in the transition states for decomposition of diazabicyclo-[2.1.0]pentane derivatives has been demonstrated by
    • Strong conformational preferences in the transition states for decomposition of diazabicyclo-[2.1.0]pentane derivatives has been demonstrated by J. A. Berson and S. S. Olin, J. Amer. Chem. Soc., 91, 777 (1969).
    • (1969) J. Amer. Chem. Soc. , vol.91 , pp. 777
    • Berson, J.A.1    Olin, S.S.2
  • 91
    • 37049163420 scopus 로고
    • That thiocarbonyl ylides should be nonlinear follows directly from application of Walsh's rules: (a) 2288, 2296, 2301
    • That thiocarbonyl ylides should be nonlinear follows directly from application of Walsh's rules: (a) A. D. Walsh, J. Chem. Soc., 2260, 2266, 2288, 2296, 2301 (1953);
    • (1953) J. Chem. Soc. , vol.2260 , pp. 2266
    • Walsh, A.D.1
  • 94
    • 85022716460 scopus 로고
    • For a general review of the geometry of sulfur compounds, see
    • For a general review of the geometry of sulfur compounds, see S. C. Abrahams, Quart. Rev., X, 407 (1956).
    • (1956) Quart. Rev., X , pp. 407
    • Abrahams, S.C.1
  • 105
    • 33644840918 scopus 로고
    • the reason for the discrepancy in melting point is unknown
    • M. A. Youtz and P. P. Perkins, J. Amer. Chem. Soc., 51, 3508 (1929); the reason for the discrepancy in melting point is unknown.
    • (1929) J. Amer. Chem. Soc. , vol.51 , pp. 3508
    • Youtz, M.A.1    Perkins, P.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.