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Volumn 65, Issue 28, 2009, Pages 5596-5607

Practical and robust method for stereoselective preparations of ketene silyl (thio)acetal derivatives and NaOH-catalyzed crossed-Claisen condensation between ketene silyl acetals and methyl esters

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL DERIVATIVE; ESTER DERIVATIVE; KETENE DERIVATIVE; SILANE DERIVATIVE; SODIUM HYDROXIDE; THIOACETALDEHYDE;

EID: 66349097720     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.02.084     Document Type: Article
Times cited : (12)

References (74)
  • 2
    • 35348849775 scopus 로고
    • Trost B.M., and Fleming I. (Eds), Pergamon, Oxford
    • Gennari C. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 2 (1991), Pergamon, Oxford 630-657
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 630-657
    • Gennari, C.1
  • 6
    • 66349116211 scopus 로고    scopus 로고
    • Ref. 1a, p 1132;
    • Ref. 1a, p 1132;
  • 10
    • 34247266658 scopus 로고    scopus 로고
    • Commercially available. Compared with ether solvents such as THF, dioxolane, DME, etc. there are several advantages for process chemistry:
    • Commercially available. Compared with ether solvents such as THF, dioxolane, DME, etc. there are several advantages for process chemistry:. Watanabe K., Yamagiwa N., and Torisawa Y. Org. Process Res. Dev. 11 (2007) 251
    • (2007) Org. Process Res. Dev. , vol.11 , pp. 251
    • Watanabe, K.1    Yamagiwa, N.2    Torisawa, Y.3
  • 70
    • 15844376790 scopus 로고    scopus 로고
    • 2 is discussed. We consider that this linear TS model is significantly different from the present case
    • 2 is discussed. We consider that this linear TS model is significantly different from the present case
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 4322
    • Evans, D.A.1    Dart, M.J.2    Duffy, J.L.3    Yang, M.G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.