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Volumn 63, Issue 25, 1998, Pages 9517-9523

Preparation of chlorosilyl enolates

Author keywords

[No Author keywords available]

Indexed keywords

ESTER DERIVATIVE; KETONE DERIVATIVE; THIOL DERIVATIVE;

EID: 0032509531     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo981740h     Document Type: Article
Times cited : (41)

References (41)
  • 21
    • 20644439468 scopus 로고    scopus 로고
    • note
    • All acetate enolates in this study were contaminated with small quantities of the corresponding C-silyl isomer. Complete removal is neither necessary, nor practical, as the O-silyl enolate does isomerize slowly, even when stored at -20 °C.
  • 25
    • 0000190244 scopus 로고
    • The corresponding lithium enolate has been used in aldol reactions by Heathcock, see: (a) Heathcock, C. H.; Young, S. D.; Hagen, J. P.; Pirrung, M. C.; White, C. T.; VanDerveer, D. J. Org. Chem. 1980, 45, 3846. (b) Heathcock, C. H.; Pirrung, M. C.; Montgomery, S. H, Lampe, J. Tetrahedron 1981, 37, 4087.
    • (1981) Tetrahedron , vol.37 , pp. 4087
    • Heathcock, C.H.1    Pirrung, M.C.2    Montgomery, S.H.3    Lampe, J.4
  • 27
    • 0001715120 scopus 로고
    • For leading references on alkyltin enolates see: (a) Yasuda, M.; Katoh, Y.; Shibata, I.; Baba, A.; Matsuda, H.; Sonoda, N. J. Org. Chem. 1994, 59, 4386. (b) Shibata, I.; Baba, A. Org. Prep. Proced. Int. 1994, 26, 85. Recently, an interesting asymmetric aldol addition utlizing such stannanes directly has appeared appeared; see: (c) Yanagisawa, A.; Matsumoto, Y.; Nakashima, H.; Asakawa, K.; Yamamoto, H. J. Am. Chem. Soc. 1997, 119, 9319.
    • (1994) J. Org. Chem. , vol.59 , pp. 4386
    • Yasuda, M.1    Katoh, Y.2    Shibata, I.3    Baba, A.4    Matsuda, H.5    Sonoda, N.6
  • 28
    • 21344491698 scopus 로고
    • For leading references on alkyltin enolates see: (a) Yasuda, M.; Katoh, Y.; Shibata, I.; Baba, A.; Matsuda, H.; Sonoda, N. J. Org. Chem. 1994, 59, 4386. (b) Shibata, I.; Baba, A. Org. Prep. Proced. Int. 1994, 26, 85. Recently, an interesting asymmetric aldol addition utlizing such stannanes directly has appeared appeared; see: (c) Yanagisawa, A.; Matsumoto, Y.; Nakashima, H.; Asakawa, K.; Yamamoto, H. J. Am. Chem. Soc. 1997, 119, 9319.
    • (1994) Org. Prep. Proced. Int. , vol.26 , pp. 85
    • Shibata, I.1    Baba, A.2
  • 29
    • 0030827816 scopus 로고    scopus 로고
    • For leading references on alkyltin enolates see: (a) Yasuda, M.; Katoh, Y.; Shibata, I.; Baba, A.; Matsuda, H.; Sonoda, N. J. Org. Chem. 1994, 59, 4386. (b) Shibata, I.; Baba, A. Org. Prep. Proced. Int. 1994, 26, 85. Recently, an interesting asymmetric aldol addition utlizing such stannanes directly has appeared appeared; see: (c) Yanagisawa, A.; Matsumoto, Y.; Nakashima, H.; Asakawa, K.; Yamamoto, H. J. Am. Chem. Soc. 1997, 119, 9319.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 9319
    • Yanagisawa, A.1    Matsumoto, Y.2    Nakashima, H.3    Asakawa, K.4    Yamamoto, H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.