A clean procedure for synthesis of pyrido[d]pyrimidine derivatives under solvent-free conditions catalyzed by zro2 nanoparticles

Combinatorial Chemistry and High Throughput Screening

Volumn 15, Issue 5, 2012, Pages 395-399

  Abdolmohammadi, Shahrzad ^a   Balalaie, Saeed ^b  

^a ISLAMIC AZAD UNIVERSITY   (Iran)

^b K N TOOSI UNIVERSITY OF TECHNOLOGY   (Iran)

Author keywords

Solvent free; Tandem knoevenagel michael addition; Tetrahydropyrido d pyrimidine; ZrO2 nanoparticles

Indexed keywords

4(6) AMINOURACIL; 7 AMINO 2,4 DIOXO 5 (2 CHLOROPHENYL) 1,2,3,4 TETRAHYDROPYRIDO[2,3 D]PYRIMIDINE 6 CARBONITRILE; 7 AMINO 2,4 DIOXO 5 (2,4 DICHLOROPHENYL) 1,2,3,4 TETRAHYDROPYRIDO[2,3 D]PYRIMIDINE 6 CARBONITRILE; 7 AMINO 2,4 DIOXO 5 (3 HYDROXYPHENYL) 1,2,3,4 TETRAHYDROPYRIDO[2,3 D]PYRIMIDINE 6 CARBONITRILE; 7 AMINO 2,4 DIOXO 5 (3 NITROPHENYL) 1,2,3,4 TETRAHYDROPYRIDO[2,3 D]PYRIMIDINE 6 CARBONITRILE; 7 AMINO 2,4 DIOXO 5 (4 METHOXYPHENYL) 1,2,3,4 TETRAHYDROPYRIDO[2,3 D]PYRIMIDINE 6 CARBONITRILE; 7 AMINO 2,4 DIOXO 5 (4 METHYPHENYL) 1,2,3,4 TETRAHYDROPYRIDO[2,3 D]PYRIMIDINE 6 CARBONITRILE; 7 AMINO 2,4 DIOXO 5 PHENYL 1,2,3,4 TETRAHYDROPYRIDO[2, 3 D]PYRIMIDINE 6 CARBONITRILE; MALONONITRILE; NANOPARTICLE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG; URACIL DERIVATIVE; ZIRCONIUM OXIDE NANOPARTICLE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CHEMICAL STRUCTURE; CYCLIZATION; KNOEVENAGEL CONDENSATION; ONE POT SYNTHESIS; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION TIME;

CATALYSIS; COMBINATORIAL CHEMISTRY TECHNIQUES; NANOPARTICLES; NITRILES; PYRIMIDINES; SOLVENTS; URACIL; ZIRCONIUM;

EID: 84860548352     PISSN: 13862073     EISSN: 18755402     Source Type: Journal    
DOI: 10.2174/138620712800194486     Document Type: Article

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