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Volumn 37, Issue 39, 1996, Pages 7095-7098

Catalytic asymmetric allylation of aldehydes with BINOL-Ti(IV) complex accelerated by i-PrSSiMe3

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALLYL COMPOUND;

EID: 0030599244     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01582-1     Document Type: Article
Times cited : (59)

References (26)
  • 17
    • 0029913899 scopus 로고    scopus 로고
    • 5. Recently, chiral poisoning method which allowed the use of inexpensive racemic BINOL has been reported, see: Faller, J. W.; Sams, D. W. I.; Liu, X. J. Am. Chem. Soc. 1996, 118, 1217-1218. And also, for new catalytic system (S)-BINAP-AgOTf (5 mol %), see: Yanagisawa, A.; Nakashima, H.; Ishiba, A.; Yamamoto, H. J. Am. Chem. Soc. 1996, 118, 4723-4724.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 1217-1218
    • Faller, J.W.1    Sams, D.W.I.2    Liu, X.3
  • 18
    • 0029895814 scopus 로고    scopus 로고
    • 5. Recently, chiral poisoning method which allowed the use of inexpensive racemic BINOL has been reported, see: Faller, J. W.; Sams, D. W. I.; Liu, X. J. Am. Chem. Soc. 1996, 118, 1217-1218. And also, for new catalytic system (S)-BINAP-AgOTf (5 mol %), see: Yanagisawa, A.; Nakashima, H.; Ishiba, A.; Yamamoto, H. J. Am. Chem. Soc. 1996, 118, 4723-4724.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 4723-4724
    • Yanagisawa, A.1    Nakashima, H.2    Ishiba, A.3    Yamamoto, H.4
  • 19
    • 37049052375 scopus 로고
    • 3SiCl except commercially available phenylthiotrimethylsilane, see: Abel, E. W. J. Chem, Soc. 1960, 4406-4409.
    • (1960) J. Chem, Soc. , pp. 4406-4409
    • Abel, E.W.1
  • 25
    • 85030278622 scopus 로고    scopus 로고
    • note
    • 2 compared with other solvents such as toluene, diethyl ether, and propionitrile.
  • 26
    • 85030279196 scopus 로고    scopus 로고
    • note
    • 10. The O-silylated homoallylic alcohols were isolated in good yields after aqueous work up procedure.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.