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Volumn 53, Issue 16, 1997, Pages 5909-5924

Highly enantio- and diastereoselective boron aldol reactions of α-heterosubstituted thioacetates with aldehydes and silyl imines

Author keywords

[No Author keywords available]

Indexed keywords

AZIRIDINE DERIVATIVE; FLORFENICOL; THIAMPHENICOL; THIOESTER;

EID: 0030957591     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00251-2     Document Type: Article
Times cited : (49)

References (105)
  • 1
    • 0003417469 scopus 로고
    • Pergamon Press, Oxford, Heathcock, C.H. editor
    • For reviews on the aldol reaction, see: "Comprehensive Organic Synthesis", ed. Trost, B.M. and Fleming, I., Pergamon Press, Oxford, 1991, Vol.2 (Heathcock, C.H. editor):
    • (1991) Comprehensive Organic Synthesis , vol.2
    • Trost, B.M.1    Fleming, I.2
  • 2
    • 0342568184 scopus 로고    scopus 로고
    • chapter 1.5, page 133-179; chapter 1.6, page 181-238
    • (a) Heathcock, C.H., chapter 1.5, page 133-179; chapter 1.6, page 181-238;
    • Heathcock, C.H.1
  • 4
    • 0343873916 scopus 로고    scopus 로고
    • chapter 1.9, page 301-319
    • Paterson, I., chapter 1.9, page 301-319.
    • Paterson, I.1
  • 20
    • 0000733768 scopus 로고
    • Trost B.M. and Fleming, I. Eds., Pergamon Press, Oxford
    • (h) Kleinman, E.F. in Comprehensive Organic Synthesis, Trost B.M. and Fleming, I. Eds., Pergamon Press, Oxford, 1991, Volume 2, pp. 893.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 893
    • Kleinman, E.F.1
  • 72
    • 33751386824 scopus 로고
    • N-trimethylsilylimines are known to be more reactive than N-alkyl or N-aryl imines due to the presence of a TMS group as substituent of the iminic nitrogen which increases the electrophilicity of the iminic carbon, see: (a) Bernardi, F.; Bongini, A.; Cainelli, G.; Robb, M.A.; Suzzi Valli, G. J. Org. Chem. 1993, 58, 750;
    • (1993) J. Org. Chem. , vol.58 , pp. 750
    • Bernardi, F.1    Bongini, A.2    Cainelli, G.3    Robb, M.A.4    Suzzi Valli, G.5
  • 77
    • 0029655342 scopus 로고    scopus 로고
    • For a discussion using similar chair-and boat-like transition state models, see: (a) Ishihara, T.; Ichihara, K.; Yamanaka, H. Tetrahedron 1996, 52, 255;
    • (1996) Tetrahedron , vol.52 , pp. 255
    • Ishihara, T.1    Ichihara, K.2    Yamanaka, H.3
  • 93
    • 0031013920 scopus 로고    scopus 로고
    • For the stereochemical assignment of syn and anti halohydrins based on NMR methods, see: Pridgen, L.N.; De Brosse, C. J.Org.Chem. 1997, 62, 216.
    • (1997) J. Org. Chem. , vol.62 , pp. 216
    • Pridgen, L.N.1    De Brosse, C.2
  • 94
    • 85099488357 scopus 로고    scopus 로고
    • note
    • 4-; X = Br, Cl); see the experimental section.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.