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1 CRITERII DE EVALUARE a performanţelor ştiinţifice individuale ...

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thermochromism of a series of<br />

spirocyclic compounds and color<br />

formers with heterocyclic parts<br />

and O or N as the keyatom<br />

6 Tab.5b nr.13 Synthesis of some novel 3-[(2hydrazono)benzimidazolyl]-2indolinones<br />

as possible azodyes<br />

7 Tab.1a nr.4 Vilsmeier-Haack formyaltion of<br />

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Chim.<br />

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1460<br />

Heterocycl.<br />

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pyrazolin-5-ones<br />

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8 Tab.1a nr 4 Tautomerism, acid dissociation Rev.Roum. 1997 42(9) 767-775 0.219<br />

equilibria and azocoupling<br />

reaction rates of 1-(2pyrimidinyl)-3-methylpyrazolin-<br />

5-one derivatives<br />

Chim.<br />

9 Tab.5b,nr.7 Synthesis and structural insights Heterocycl. 1998 4(2) 157-162 0.342<br />

of novel 2-diethylamino-6methyl-4-(3H)-pyrimidones<br />

Commun<br />

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derivatives with potential<br />

biological activity<br />

Chim.<br />

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structural and computational<br />

study of 2-diethylamino-6methyl-5-n-propyl-4-(3H)pyrimidone<br />

Struct.Chem. 1999 10(4) 303-310 1.537<br />

12 Tab.1a nr.6 1-(Acridin-9’-yl)-pyrazolin-3 Heterocycl. 1999 5(6) 543-548 0.342<br />

and 5-ones.A new class of<br />

heterocycles with potential<br />

biological activity<br />

Commun.<br />

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matic amines at milimolar level Chem<br />

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pirimidinil)-5-pirazolone Chimie<br />

1 7b Tab.5b nr.10 Condensation des pyrimidinyl-1- Studia UBB 1988 33(2) 61-64<br />

pyrazolones-5- avec des<br />

aldehydes aromatiques<br />

Chem<br />

2 Tab.1a nr.2 Reactivity of substituted 6- Zh.Obsch. 1998 68(5) 865-866<br />

chloro-7-diethylsulfamoyl-9thioacridones<br />

Khim.<br />

3 Tab.5b nr.15 A novel nontautomeric Studia UBB 1996 41(1) 35-42<br />

oxopyrimidine:synthesis and<br />

characterization of 2-diethylamino-5,5,6-trimethyl-4(5H)<br />

pyrimidine<br />

Chem<br />

4 Tab.5b nr.10 si Logarithmic extrapolation Studia UBB 2003 48(2) 85-90<br />

Tab.1a, nr 4 method for kinetic determination Chem<br />

of amine mixtures<br />

0.219

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