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Volumn 70, Issue 2, 2005, Pages 247-258

Sonogashira cross-coupling in the synthesis of acyclic nucleoside phosphonates: Preparation of 6-[(phosphonomethoxy)alkynyl]- and 6-[(phosphonomethoxy)alkyl]pyrimidines

Author keywords

Acyclic nucleoside phosphonates; Alkynes; Antivirals; Cross coupling reactions; Hydrogenation; Nucleosides; Nucleotide analogues; Pyrimidines; Sonogashira reaction

Indexed keywords

2 AMINO 4 CHLORO 6 [3 [(DIISOPROPOXYPHOSPHORYL)METHOXY]PROP 1 YN 1 YL]PYRIMIDINE; 2 AMINO 4 CHLORO 6 BIS[3 [(DIISOPROPOXYPHOSPHORYL)METHOXY]PROP 1 YN 1 YL]PYRIMIDINE; 2 AMINO 4 HYDROXY 6 [3 (PHOSPHOMETHOXY)PROP 1 YN 1 YL]PYRIMIDINE; 2 AMINO 4 HYDROXY 6 [3 (PHOSPHOMETHOXY)PROPYL]PYRIMIDINE; 2 AMINO 4 HYDROXY 6 [3 [(DIISOPROPOXYPHOSPHORYL)METHOXY]PROP 1 YN 1 YL]PYRIMIDINE; 2 AMINO 4,6 BIS(3 HYDROXYPROPYL)PYRIMIDINE; 2,4 DIAMINO 6 (3 HYDROXYPROPYL)PYRIMIDINE; 2,4 DIAMINO 6 (4 HYDROXYBUTYL)PYRIMIDINE; 2,4 DIAMINO 6 [3 (PHOSPHOMETHOXY)BUTYL]PYRIMIDINE; 2,4 DIAMINO 6 [3 (PHOSPHOMETHOXY)PROP 1 YN 1 YL]PYRIMIDINE; 2,4 DIAMINO 6 [3 (PHOSPHOMETHOXY)PROPYL]PYRIMIDINE; 2,4 DIAMINO 6 [3 [(DIISOPROPOXYPHOSPHORYL)METHOXY]PROP 1 EN 1 YL]PYRIMIDINE; 2,4 DIAMINO 6 [3 [(DIISOPROPOXYPHOSPHORYL)METHOXY]PROP 1 YN 1 YL]PYRIMIDINE; 2,4 DIAMINO 6 [3 [(DIISOPROPOXYPHOSPHORYL)METHOXY]PROPYL]PYRIMIDINE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 17744366648     PISSN: 00100765     EISSN: None     Source Type: Journal    
DOI: 10.1135/cccc20050247     Document Type: Article
Times cited : (7)

References (16)
  • 1
    • 0000002872 scopus 로고
    • E. De Clercq, Ed., JAI Press, Greenwich (CT)
    • Reviews: a) Holý A. in: Advances in Antiviral Drug Design (E. De Clercq, Ed.), p. 179. JAI Press, Greenwich (CT) 1994; b) Holý A. in: Recent Advances in Nucleosides: Chemistry and Chemotherapy (C. K. Chu, Ed.), p. 167. Elsevier Science B.V., Amsterdam 2002; c) Holý A.: Curr. Pharm. Des. 2003, 2567.
    • (1994) Advances in Antiviral Drug Design , pp. 179
    • Holý, A.1
  • 2
    • 0142171945 scopus 로고    scopus 로고
    • C. K. Chu, Ed., Elsevier Science B.V., Amsterdam
    • Reviews: a) Holý A. in: Advances in Antiviral Drug Design (E. De Clercq, Ed.), p. 179. JAI Press, Greenwich (CT) 1994; b) Holý A. in: Recent Advances in Nucleosides: Chemistry and Chemotherapy (C. K. Chu, Ed.), p. 167. Elsevier Science B.V., Amsterdam 2002; c) Holý A.: Curr. Pharm. Des. 2003, 2567.
    • (2002) Recent Advances in Nucleosides: Chemistry and Chemotherapy , pp. 167
    • Holý, A.1
  • 3
    • 17744368339 scopus 로고    scopus 로고
    • Reviews: a) Holý A. in: Advances in Antiviral Drug Design (E. De Clercq, Ed.), p. 179. JAI Press, Greenwich (CT) 1994; b) Holý A. in: Recent Advances in Nucleosides: Chemistry and Chemotherapy (C. K. Chu, Ed.), p. 167. Elsevier Science B.V., Amsterdam 2002; c) Holý A.: Curr. Pharm. Des. 2003, 2567.
    • (2003) Curr. Pharm. Des. , pp. 2567
    • Holý, A.1
  • 4
    • 0032378483 scopus 로고    scopus 로고
    • For reviews, see: a) De Clercq E.: Collect. Czech. Chem. Commun. 1998, 63, 480; b) Snoeck R., Noel J. C., Muller C., De Clercq E., Bossens M.: J. Med. Virol. 2000, 60, 205.
    • (1998) Collect. Czech. Chem. Commun. , vol.63 , pp. 480
    • De Clercq, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.