265 results on '"Nemeryuk, M. P."'
Search Results
2. Synthesis and properties of dipyrimido-[4,5-b][5,4-f]-1,4-thiazepine derivatives
3. Synthesis, properties, and reactions of derivatives of 1,3-dimethyl-6-(5′-aminopyrimidylthio-6′)uracils
4. Conversions of Coumarins Accompanied by Intermediate Opening and Recyclization of the Lactone Ring. 2. Study of the Interaction of Malonic Acid Hydrazide and Amide Derivatives with 3-Acyl(3-cyano, 3-ethoxycarbonyl)Coumarins
5. Study of Nitrogen- and Sulfur-Containing Heterocycles. 57. Synthesis and Conversion of 4′-Substituted 5-(5-Amino-6-Pyrimidylthio)-2,2-Dimethyl-4,6-Dioxo-1,3-Dioxanes
6. Study of nitrogen- and sulfur-containing heterocycles. 54. Properties and conversions of pyrimido[4,5-b]-1,4-benzothiazepines. Synthesis of a novel heterocyclic system: Pyrimido[5,4-c]isoquinoline
7. Conversion of Coumarins Accompanied by Opening and Recyclization of the Lactone Ring. 1. Study of the Reaction of 3-Ethoxycarbonyl(3-acyl)coumarins with Cyanoacetylhydrazine and Its Derivatives
8. Synthesis and Biological Properties of Arylthio-1,2,3-Triazole Derivatives
9. Investigation of Nitrogen- and Sulfur-containing Heterocycles. 53. Reactions of 5-Amino-6-mercaptopyrimidines with Derivatives of p-Chloronitrobenzene. Synthesis of a New Heterocyclic System - Pyrimido[4,5-b]-1,4-benzothiazepine
10. Synthesis and pharmacological properties of 4(5)-substituted 5(4)-amidino-1,2,3-triazoles
11. Structure of cyanoethylation products of 1,2,3-triazolecarboxylic acid derivatives
12. 4-dialkyldithiocarbamoyl-5-nitropyrimidines. Synthesis, structure, properties
13. Highly polarized enamines 1. synthesis and some properties ofβ-tetrazolylenamines
14. Investigation of bis-heteryl derivatives of piperazine and its analogs 1. Synthesis and conversions of n,n′-bis(2-r-5-nitro-6-pyrimidinyl)piperazines and n,n3-bis(2-r-5-nitro-6-pyrimidinyl)dispirotripiperazinium dichloride
15. Reactions of 4(6)-chloro-5-nitropyrimidines with nucleophilic agents (review)
16. Hetero analogs of alloxazines 3. Rearrangements of 6,8-dimethyl-9a-hydroxy-7,9-dioxo-9ah-6,7,8,9-tetrahydrodipyrimido[4,5-b][4′,5′-e][1,4]thiazines
17. Hetero analogs of alloxazines. 2. Structure and tautomerism of 6,8-dimethyl-7,9-dioxo-5h-6,7,8,9-tetrahydropyrimido[4,5-b][4′,5′-e][1,4]thiazines
18. Heteroanalogs of alloxazines: 1. Properties and conversions of 6,8-dimethyl-7,9-dioxo-5h-6,7,8,9-tetrahydropyrimido[4,5-b]-[4′,5′-e][1,4]thiazines
19. Derivatives of 4(5)substituted-1,2,3-triazol-5(4)-carboxylic acids synthesis and antitumor activity
20. NEW APPROACH TO THE SYNTHESIS OF 3-ARYLCOUMARINS. REACTION OF 3-ACYL- AND 3-ETHOXYCARBONYLCOUMARINS WITH HYDRAZIDE OF p-NITROPHENYLACETIC ACID
21. Investigation of bisheteryl derivatives of piperazine and its analogs. 2. Synthesis and properties of bis(dialkyldithiocarbamoyl-5-nitro-4-pyrimidyl)piperazines
22. One-pot synthesis of N-(3-coumarinoyl-)-N′-(salicylidene)hydrazines from 3-ethoxycarbonyl-(acyl)coumarins
23. Synthesis and pharmacokinetics of sodium [35S]-3-aurothio-2-hydroxypropanesulfonate
24. Conversion of 4-chloro-5-nitropyrimidines to 1,3,5-triazines using alkylisothioureas
25. Derivatives of dihydropyrimido (4,5-b)-(1,4) benzthiazine and their pharmacological properties
26. Derivatives of condensed pyrimidine, pyrazine, and pyridine systems. 39. Synthesis and structures of 9-oxo-5H-6,7,8,9-tetrahydropyrimido[4,5-b][1,4]thiazines
27. Derivatives of condensed pyrimidine, pyrazine, and pyridine systems: XXXIII. 6-Aminopyrimido[4,5-b]-1,4-thiazines
28. 1-Nucleosides of 5-substituted 4-chloro-1,2,3-triazoles
29. Synthesis and pharmacokinetics of the hydrochloride of [14C]-6-amino-4-methoxypyrimido[4,5-b][1,4]thiazine
30. Synthesis of deuterium- and tritium-labeled 4-methoxy-6-amino-pyrimido[4,5,b](1,4)-thiazine hydrochloride
31. Chemistry of folic acid antagonists (a review)
32. Structure of the cationic forms of pyrimido [4,5-b][1,4]thiazines — A new type of folic acid antagonist
33. 6,7,8,9-Tetrahydrodipyrimido[4,5-b][4′,5′-e][1,4]thiazine derivatives. Synthesis and structure
34. Synthesis and biological properties of pyrimido[4.5-b][1.4]-thiazine derivatives
35. Synthesis of sulfur-labelled 4-methylthio-6-aminopyrimido (4,5-b)(1, 4)thiazine and its distribution in organisms
36. Investigation of the z, e isomerism of N-(5-pyrimidyl)- and N-(5-pyridyl) acetamidines
37. An algorithmic search for folic acid antagonists in a series of pyrimido[4,5-b](1,4)thiazines
38. Amino-derivatives of 4-methoxy-7,8-dihydro-1,3-diazaphenothiazine and their neurotropic activity
39. Synthesis and pharmacological properties of 4,9-diamino derivatives of 7,8-dihydro-1,3-diazaphenothiazine
40. An algorithmic search for folic acid antagonists in the pyrimido[4,5-b][1,4]benzothiazine series
41. Synthesis and pharmacological properties of 4-piperazinyl-9-oxo-6,7,8,9-tetrahydropyrimido [4,5-b](1,4)benzothiazines
42. Synthesis of35S-tomisine and its distribution in the organism of the rat
43. Derivatives of condensed systems based on pyrimidine, pyrazine, and pyridine: XXXVI. Synthesis of pyrimido[4,5-b]-1,4-thiazin-6-ones and pyrimido[4,5-b]-1,5-thiazepin-6-ones
44. Pyrimido(4,5-b)(1,4)thiazine derivatives. A new type of folic acid antagonist
45. Investigation of nitrogen- and sulfur-containing heterocycles: XXIII. Synthesis of 6-amino derivatives of pyrimido[4,5-b]-,pyrazino[2,3-b]-, and pyrido[2,3-b]-1,4-thiazines
46. Nitrogen- and sulfur-containing heterocycles: XIX. 7H-4-chloro-6-aryl- and 5H-pyrimido[4,5-b][1,4]thiazines
47. Researches on nitrogen and sulfur heterocyclic rings: IV. Pyrimido[4, 5-b]-[1, 4]thiazines
48. Investigation of nitrogen- and sulfur-containing heterocycles: V. The reaction of 5-amino-6-mercaptopyrimidines with phenacyl chlorides
49. Investigation of nitrogen- and sulfurcontaining heterocycles: XVI. Reaction of 5-amino-6-mercaptopyrimidines with haloketo acid esters
50. Synthesis of 4-methoxypyrimido[4, 5-b][1,4]thiazin-6-one-S35 and its distribution in the body
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.