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Volumn , Issue 8, 2003, Pages 1105-1108

Facile removal strategy for allyl and allyloxycarbonyl protecting groups using solid-supported barbituric acid under palladium catalysis

Author keywords

Allyl and allyloxycarbonyl groups; Facile isolation; Highly polar compounds; Palladium(0) catalyzed deprotection; Solid supported barbituric acid

Indexed keywords

ALLYL COMPOUND; AMINE; BARBITURIC ACID; CARBAMIC ACID DERIVATIVE; CARBONIC ACID DERIVATIVE; CARBONYL DERIVATIVE; ESTER; ETHER DERIVATIVE; PALLADIUM; REAGENT;

EID: 0038391497     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-39907     Document Type: Article
Times cited : (18)

References (18)
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    • 0034533265 scopus 로고    scopus 로고
    • Recent reviews on solid-supported reagents, see: (a) Bhalay, G.; Dunstan, A.; Glen, A. Synlett 2000, 1846.(b) Ley, S. V.; Baxendle, I. R.; Bream, R. N.; Jackson, P. S.; Leach, A. G.; Longbottom, D. A.; Nesi, M.; Scott, J. S.; Storer, R. I.; Taylor, S. J. J. Chem. Soc., Perkin Trans. 1 2000, 3815. (c) Kirshning, A.; Monenschein, H.; Wittenberg, R. Angew. Chem. Int. Ed. 2001, 40, 650.
    • (2000) Synlett , pp. 1846
    • Bhalay, G.1    Dunstan, A.2    Glen, A.3
  • 4
    • 0035804384 scopus 로고    scopus 로고
    • Recent reviews on solid-supported reagents, see: (a) Bhalay, G.; Dunstan, A.; Glen, A. Synlett 2000, 1846.(b) Ley, S. V.; Baxendle, I. R.; Bream, R. N.; Jackson, P. S.; Leach, A. G.; Longbottom, D. A.; Nesi, M.; Scott, J. S.; Storer, R. I.; Taylor, S. J. J. Chem. Soc., Perkin Trans. 1 2000, 3815. (c) Kirshning, A.; Monenschein, H.; Wittenberg, R. Angew. Chem. Int. Ed. 2001, 40, 650.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 650
    • Kirshning, A.1    Monenschein, H.2    Wittenberg, R.3
  • 9
    • 0038486498 scopus 로고    scopus 로고
    • note
    • 2P (1 x 40 mL) to give la (6.24 g, quant.).
  • 12
    • 0019940681 scopus 로고
    • The synthesis of 1a according to the following report on solution-phase synthesis of barbituric acids was also unsuccessful: Yogo, M.; Hirota, K.; Senda, S. Chem. Pharm. Bull. 1982, 30, 1333.
    • (1982) Chem. Pharm. Bull. , vol.30 , pp. 1333
    • Yogo, M.1    Hirota, K.2    Senda, S.3
  • 13
    • 0038147827 scopus 로고
    • Chem. Abstr. 1984, 101, 151878.
    • (1984) Chem. Abstr. , vol.101 , pp. 151878
  • 15
    • 0038147828 scopus 로고    scopus 로고
    • Chem. Abstr. Recently, a solid-phase synthesis of barbituric acid libraries was reported, in which the polymer-supported urea was silylated, condensed with Meldrum's acid and cyclized to give the barbituric acid derivatives. Our method is superior to this one in its simplicity: 2000, 133, 164060.
    • (2000) Chem. Abstr. , vol.133 , pp. 164060
  • 16
  • 17
    • 0038824459 scopus 로고    scopus 로고
    • note
    • + 527.1379. Found: 527.1401.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.