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Volumn 8, Issue 9, 1997, Pages 1339-1367

Chiral sulfinyl-1,3-dienes. Synthesis and use in asymmetric reactions

Author keywords

[No Author keywords available]

Indexed keywords

ORGANOSULFUR DERIVATIVE; SULFENIC ACID DERIVATIVE; SULFONE; SULFOXIDE; THIOPHENE DERIVATIVE;

EID: 0030914724     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00158-4     Document Type: Review
Times cited : (69)

References (104)
  • 1
    • 0026661770 scopus 로고
    • Walker, A.J. Tetrahedron: Asymmetry 1992, 3, 961-998; Solladié, G.; Carreño, M.C. Organosulfur Chem. 1995, 1-47; Carreño, M.C. Chem. Rev. 1995, 95, 1717-1760.
    • (1992) Tetrahedron: Asymmetry , vol.3 , pp. 961-998
    • Walker, A.J.1
  • 2
    • 0010485175 scopus 로고
    • Walker, A.J. Tetrahedron: Asymmetry 1992, 3, 961-998; Solladié, G.; Carreño, M.C. Organosulfur Chem. 1995, 1-47; Carreño, M.C. Chem. Rev. 1995, 95, 1717-1760.
    • (1995) Organosulfur Chem. , pp. 1-47
    • Solladié, G.1    Carreño, M.C.2
  • 3
    • 11944251609 scopus 로고
    • Walker, A.J. Tetrahedron: Asymmetry 1992, 3, 961-998; Solladié, G.; Carreño, M.C. Organosulfur Chem. 1995, 1-47; Carreño, M.C. Chem. Rev. 1995, 95, 1717-1760.
    • (1995) Chem. Rev. , vol.95 , pp. 1717-1760
    • Carreño, M.C.1
  • 4
    • 0003942864 scopus 로고
    • John Wiley & Sons, Inc.: New York
    • The term 'chiral' is used to mean that the substance is made up of chiral molecules, including all the intermediate situations between the two extreme ones, i.e. enantiopure and racemic samples. See Eliel, E.L.; Wilen, S.H. Stereochemistry of Organic Compounds; John Wiley & Sons, Inc.: New York, 1994; pp. 4-5.
    • (1994) Stereochemistry of Organic Compounds , pp. 4-5
    • Eliel, E.L.1    Wilen, S.H.2
  • 6
  • 13
    • 0141583854 scopus 로고
    • (b) Synth. Commun. 1981, 11, 697-708;
    • (1981) Synth. Commun. , vol.11 , pp. 697-708
  • 54
    • 0000270134 scopus 로고
    • Rémion, J.; Krief, A. Tetrahedron Lett. 1976, 41, 3743-3746; Reich, H.J.; Chow, F.; Shah, S.K. J. Am. Chem. Soc. 1979, 101, 6638-6648.
    • (1976) Tetrahedron Lett. , vol.41 , pp. 3743-3746
    • Rémion, J.1    Krief, A.2
  • 62
    • 0343970673 scopus 로고    scopus 로고
    • Unpublished results
    • Unpublished results.
  • 64
    • 0342898314 scopus 로고
    • 3-Sulfolenes were reacted with Grignard reagents to give racemic 1-sulfinyl-1,3-butadienes (Gaoni, Y. Tetrahedron Lett. 1977, 4521-4524). This method seems to have the serious drawback of producing mainly (Z)-dienes, too hindered for cycloadditions. It has however been found that (Z)-1-phenylsulfinyl-1,3-butadiene [and perhaps also other (Z)-dienes] can be almost totally converted into (E)-diene by irradiation of its solutions, in the presence of iodine, with an incandescent lamp or in direct sunlight.
    • (1977) Tetrahedron Lett. , pp. 4521-4524
    • Gaoni, Y.1
  • 74
    • 0343534778 scopus 로고    scopus 로고
    • note
    • When DA adducts are formed from racemic sulfinyldienes, configurations of the new stereogenic centres, shown in the schemes, are intended as relative.
  • 79
    • 0028230251 scopus 로고
    • (b) Chem. Pharm. Bull. 1994, 42, 985-987.
    • (1994) Chem. Pharm. Bull. , vol.42 , pp. 985-987


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.