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Volumn 50, Issue 16, 2009, Pages 1838-1843

Facile conversion of Biginelli 3,4-dihydropyrimidin-2(1H)-thiones to 2-(2-hydroxy-2-arylvinyl) dihydropyrimidines via Eschenmoser coupling

Author keywords

Biginelli; DHPM; Drug research; Eschenmoser; Eschenmoser coupling; Polymer supported; Privileged structure; Sulfide contraction; Triphenylphosphine

Indexed keywords

2 (2 HYDROXY 2 ARYLVINYL) DIHYDROPYRIMIDINE; 3,4 DIHYDROPYRIMIDIN 2(1H) THIONE; PYRIMIDINE DERIVATIVE; SULFIDE; SULFUR; THIOKETONE; TRIPHENYLPHOSPHINE; UNCLASSIFIED DRUG;

EID: 61349100776     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.02.027     Document Type: Article
Times cited : (25)

References (24)
  • 14
    • 61349188394 scopus 로고    scopus 로고
    • The Merck Index, An Encyclopedia of Chemicals, Drugs and Biologicals, 13th ed., Merck Whitehouse Station, 2001.
    • The Merck Index, An Encyclopedia of Chemicals, Drugs and Biologicals, 13th ed., Merck Whitehouse Station, 2001.
  • 24
    • 61349175929 scopus 로고    scopus 로고
    • note
    • 1H NMR spectra of all products 11 show two sets of signals with approximate 3:1 intensity. This is due to different conformations of the C2-C bond as well as the possible tautomerism of the dihydropyrimidin core 11.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.