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Volumn , Issue 8, 2009, Pages 1318-1322

A convenient method for converting hydroxyacetophenones into their ethylene or trimethylene acetals

Author keywords

Acetal; Cerium(III) trifluoromethanesulfonate; Hydroxyacetophenone; Lewis acid; Protecting group

Indexed keywords

ACETAL; CATALYTIC AMOUNTS; ETHYLENE ACETAL; HYDROXYACETOPHENONE; HYDROXYACETOPHENONES; LEWIS ACID; MILD REACTION CONDITIONS; PROTECTING GROUP; TRIMETHYLENE;

EID: 67650021187     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0028-1088025     Document Type: Article
Times cited : (17)

References (30)
  • 4
    • 0003405157 scopus 로고    scopus 로고
    • 3rd ed; Georg Thieme Verlag: New York, Chap. 2
    • (d) Kocienski, P. J. Protecting Groups, 3rd ed; Georg Thieme Verlag: New York, 2004, Chap. 2.
    • (2004) Protecting Groups
    • Kocienski, P.J.1
  • 6
    • 0034908286 scopus 로고    scopus 로고
    • For ethylene acetalization of acetophenone, see: a
    • For ethylene acetalization of acetophenone, see: (a) Reddy, B. M.; Reddy, V. R.; Giridhar, D. Synth. Commun. 2001, 31, 1819.
    • (2001) Synth. Commun , vol.31 , pp. 1819
    • Reddy, B.M.1    Reddy, V.R.2    Giridhar, D.3
  • 13
    • 0000091321 scopus 로고    scopus 로고
    • For trimethylene acetalization of acetophenone, see: h
    • For trimethylene acetalization of acetophenone, see: (h) Karimi, B.; Ebrahimian, G. R.; Seradj, H. Org. Lett. 1999, 1, 1737.
    • (1999) Org. Lett , vol.1 , pp. 1737
    • Karimi, B.1    Ebrahimian, G.R.2    Seradj, H.3
  • 22
    • 0032546309 scopus 로고    scopus 로고
    • Zeolite HSZ-360-catalyzed ethylene acetalization of 3-hydroxyacetophenone was reported: Ballini, R.; Bosica, G.; Frullanti, B.; Maggi, R.; Sartori, G.; Schroer, F. Tetrahedron Lett. 1998, 39, 1615.
    • Zeolite HSZ-360-catalyzed ethylene acetalization of 3-hydroxyacetophenone was reported: Ballini, R.; Bosica, G.; Frullanti, B.; Maggi, R.; Sartori, G.; Schroer, F. Tetrahedron Lett. 1998, 39, 1615.
  • 23
    • 0037492241 scopus 로고    scopus 로고
    • 3 in other types of reactions, see: for acylation: (a) Dalpozzo, R.; De Nino, A.; Maiuolo, L.; Procopio, A.; Nardi, M.; Bartoli, G.; Romeo, R. Tetrahedron Lett. 2003, 44, 5621.
    • 3 in other types of reactions, see: for acylation: (a) Dalpozzo, R.; De Nino, A.; Maiuolo, L.; Procopio, A.; Nardi, M.; Bartoli, G.; Romeo, R. Tetrahedron Lett. 2003, 44, 5621.
  • 29
    • 67650056308 scopus 로고    scopus 로고
    • No reaction took place when the reaction was carried out in the absence of ethane-1,2-diol
    • No reaction took place when the reaction was carried out in the absence of ethane-1,2-diol.
  • 30
    • 67650048383 scopus 로고    scopus 로고
    • Cyclic acetalization of normal ketones such as octan-2-one and acetophenone proceeded smoothly under similar reaction conditions
    • Cyclic acetalization of normal ketones such as octan-2-one and acetophenone proceeded smoothly under similar reaction conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.