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Volumn 1981, Issue 3, 1981, Pages 185-196

Asymmetric synthesis using nucleophilic reagents containing a chiral sulfoxide group

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EID: 85077702395     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-1981-29378     Document Type: Article
Times cited : (475)

References (138)
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  • 4
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    • Organic Chemistry of Sulfur, S. Oae, Ed. Plenum Press, New York. 1977
    • Organic Chemistry of Sulfur, S. Oae, Ed., Plenum Press, New York. 1977.
  • 23
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    • S
    • M. Cioni et al., J. Chem. Res. (S) 1978, 270, 272, 274.
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  • 24
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    • D-J-C ram, S. H. Pine, J. Am. Chem. Soc. 85, 1096 1963
    • J. Drabowicz, S. Oae, Tetrahedron 34, 63 (1978). ^ D-J-C ram, S. H. Pine, J. Am. Chem. Soc. 85, 1096 (1963).
    • (1978) Tetrahedron , vol.34 , pp. 63
    • Drabowicz, J.1    Oae, S.2
  • 64
    • 0141578201 scopus 로고
    • for a general method of determining the absolute configuration of sulfoxides
    • S. Juge, H. B. Kagan, Tetrahedron Lett. 1975, 2733; for a general method of determining the absolute configuration of sulfoxides.
    • (1975) Tetrahedron Lett , pp. 2733
    • Juge, S.1    Kagan, H.B.2
  • 66
    • 0037949307 scopus 로고
    • An ambiguity arises in the configurational designation of sulfinate esters because the prefixes (R) and (S) are reversed according to whether the S O bonded is regarded as a single or as a double bond. We followed a previously established custom (Ref.24) and we considered for nomenclatural purposes the S-O bond as a single bond
    • C. J. M. Striling, J. Chem. Soc. 1963, 5741. An ambiguity arises in the configurational designation of sulfinate esters because the prefixes (R) and (S) are reversed according to whether the S O bonded is regarded as a single or as a double bond. We followed a previously established custom (Ref.24) and we considered for nomenclatural purposes the S-O bond as a single bond.
    • (1963) J. Chem. Soc. , pp. 5741
    • Striling, C.J.M.1
  • 83
    • 85077703651 scopus 로고
    • These authors estimated a stabilizing effect of the order of 25-42 kJ mol 1 (6-10 kcal mol ') of a carbanion « to a C, H S group
    • F. G. Bordwell, M. Van der Puy, N. R. Vanier, J. Org. Chem. 41, 1855 (1976). These authors estimated a stabilizing effect of the order of 25-42 kJ mol 1 (6-10 kcal mol ') of a carbanion « to a C, H S group.
    • (1976) J. Org. Chem. , vol.41 , pp. 1855
    • Bordwell, F.G.1    Puy, M.V.D.2    Vanier, N.R.3
  • 92
  • 106
    • 33947091734 scopus 로고
    • >7 In his paper (Ref. a) Durst quoted a wrong absolute configuration for sulfoxide (+ )-6
    • S. Wolfe, Acc. Chem. Res. 5, 102 (1972). ">7 In his paper (Ref. a) Durst quoted a wrong absolute configuration for sulfoxide (+ )-6.
    • (1972) Acc. Chem. Res , vol.5 , pp. 102
    • Wolfe, S.1
  • 132
    • 0342979849 scopus 로고
    • "4 F. Matloubi, G. Solladie, unpublished work
    • F. Matloubi, G. Solladie, Tetrahedron Lett. 1979, 2141. "4 F. Matloubi, G. Solladie, unpublished work.
    • (1979) Tetrahedron Lett , pp. 2141
    • Matloubi, F.1    Solladie, G.2


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