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Volumn 9, Issue 16, 2011, Pages 5648-5651

Direct conversion of acetals to esters with high regioselectivity via O,P-acetals

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIC ACETALS; DIRECT CONVERSION; O ,O-ACETALS; REGIOSELECTIVE CLEAVAGE; SINGLE-ISOMER;

EID: 79960986609     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c1ob05687e     Document Type: Article
Times cited : (5)

References (42)
  • 2
    • 0003463150 scopus 로고    scopus 로고
    • 1st ed.; Blackwell Science, Inc., Malden, MA, For the representative oxidation reaction of acetals to esters, see
    • J. R. Hanson, Protective Groups in Organic Synthesis, 1st ed.; Blackwell Science, Inc., Malden, MA, 1999
    • (1999) Protective Groups in Organic Synthesis
    • Hanson, J.R.1
  • 42
    • 0030767557 scopus 로고    scopus 로고
    • No other regioisomer was detected, and the O,P-acetal remained in the reaction For the regioselective oxygenation of unsymmetrical cyclic acetals, the choice of the silyltriflate is critical. When we examined the oxidation reaction with TMSOTf instead of TESOTf, the regioselectivity decreased.
    • J. Sandri T. Soto J.-L. Gras J. Viala Tetrahedron Lett. 1997 38 6611
    • (1997) Tetrahedron Lett. , vol.38 , pp. 6611
    • Sandri, J.1    Soto, T.2    Gras, J.-L.3    Viala, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.