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Volumn 44, Issue 29, 2003, Pages 5487-5490

Catalytic allylic transfer reactions of functionalized aldehydes promoted by BINOL-Ti(IV) with synergistic reagent

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DERIVATIVE; ALLYL COMPOUND; AMIDE; ESTER; KETONE; REAGENT; SULFUR DERIVATIVE; TIN; TITANIUM DERIVATIVE;

EID: 0038787991     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)01033-5     Document Type: Article
Times cited : (20)

References (23)
  • 4
    • 0001093382 scopus 로고    scopus 로고
    • For review: (a) Vogl, E. M.; Groger, H.; Shibasaki, M. Angew. Chem., Int. Ed. 1999, 38, 1571-1577; (b) Mikami, K.; Terada, M.; Korenaga, T.; Matsumoto, Y.; Ueki, M.; Angelaud, R. Angew. Chem., Int. Ed. 2000, 39, 3532-3556.
    • (1999) Angew. Chem., Int. Ed. , vol.38 , pp. 1571-1577
    • Vogl, E.M.1    Groger, H.2    Shibasaki, M.3
  • 14
    • 0001055858 scopus 로고    scopus 로고
    • Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer-Verlag: Berlin
    • Recent reviews: (a) Yanagisawa, A. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer-Verlag: Berlin, 1999; Vol. II, pp. 965-979; (b) Denmark, S. E.; Almstead, N. G. In Modern Carbonyl Chemistry; Otera, J., Ed.; Wiley-VCH: Weiheim, 2000; pp. 299-401.
    • (1999) Comprehensive Asymmetric Catalysis , vol.2 , pp. 965-979
    • Yanagisawa, A.1
  • 15
    • 0000554723 scopus 로고    scopus 로고
    • Otera, J., Ed.; Wiley-VCH: Weiheim
    • Recent reviews: (a) Yanagisawa, A. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer-Verlag: Berlin, 1999; Vol. II, pp. 965-979; (b) Denmark, S. E.; Almstead, N. G. In Modern Carbonyl Chemistry; Otera, J., Ed.; Wiley-VCH: Weiheim, 2000; pp. 299-401.
    • (2000) Modern Carbonyl Chemistry , pp. 299-401
    • Denmark, S.E.1    Almstead, N.G.2
  • 17
    • 0004068133 scopus 로고
    • Academic Press: New York
    • 2 for 48 h, and then careful distillation (10 mmHg, 47-49°C, 70∼80% yield), see: Pelter, A.; Smith, K.; Brown, H. C. Borane Reagents; Academic Press: New York, 1988, p. 436.
    • (1988) Borane Reagents , pp. 436
    • Pelter, A.1    Smith, K.2    Brown, H.C.3
  • 19
    • 85031161678 scopus 로고    scopus 로고
    • note
    • 3).
  • 20
    • 85031146852 scopus 로고    scopus 로고
    • note
    • Compound 12a was reduced by hydrazine hydrate in the presence of KOH to the corresponding (+)-(4R)-7-phenyl-hept-1-2n-4-ol in 41% yield. This alcohol has not only the same specific rotation sign but also identical NMR spectra of (+)-MTPA ester derivatives as compared with synthetic alcohol prepared by allyltributylstannane with 4-phenylbutanal in the presence of (S)-BINOL-Ti(VI) as described in Ref. 4a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.