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Volumn 66, Issue 41, 2010, Pages 8175-8180

Regioselective addition reactions at C-2 of 3,4-dihydropyrimidinones. Synthesis and evaluation of multifunctionalized tetrahydropyrimidines

Author keywords

Biginelli compounds; Carbon nucleophiles; Desulfurization; Pyrimidines; Regioselectivity

Indexed keywords

3,4 DIHYDROPYRIMIDINONE DERIVATIVE; CHLOROFORMIC ACID ETHYL ESTER; NUCLEOPHILE; PYRIMIDINONE DERIVATIVE; TETRAHYDROPYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77956611044     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.08.034     Document Type: Article
Times cited : (17)

References (34)
  • 22
    • 77956613162 scopus 로고    scopus 로고
    • note
    • 50: 0.9 μg/mL and 1.2 μg/mL, respectively). Compound 7 was more cytotoxic (MCC: 4-10 μg/mL) to confluent cell cultures (i.e., human embryonic lung cells, feline Crandell kidney cells) than 8 (MCC: ≥100 μg/mL) in these cell cultures. Singh, K, Arora, D, Balzarini, J. unpublished results.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.