37 results on '"Kustanovich I"'
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2. Study of the structure and inversion of 4-benzamido-trans-3-hydroxy-trans-2-carbomethoxythiophan
3. Synthesis of all of the possible stereoisomers of 4-benzamido-3-hydroxy-2-(δ-carbomethoxybutyl)thiophan
4. Change in the selectivity of the action of catalysts in the hydrogenation of the dienone group: Communication 7. Modification of nickel catalysts with lead
5. Syntheses, structures, and reactions of di- and tetrahydropyrroles: VII. Imino-enamine tautomerism of pyrrolines in solutions
6. Study of the inversion of 4-benzamido-3-hydroxythiophane
7. Nonlinear vector field having an exact particle-like solution with finite energy and phase wave
8. Change in the selectivity of the action of catalysts in the hydrogenation of the dienone group: Communication 5. Influence of modification of a Ni-Al2O3 catalyst with cadmium on the mechanism of the addition of hydrogen to 6-methyl-3, 5-heptadiene-2-one
9. Synthesis of di- and tetrahydropyrroles: VIII. Synthesis and properties of 2,3,3-trimethyl-2-hydroxy-5-pyrrolidone
10. Determination of 4-methyl-5 -propoxyoxazole and pyridoxine acetal
11. Spectrophotometric determination of the intermediates in the synthesis of 4-amino(desoxy)-10-methylpteroyl-1-glutamic acid
12. Syntheses of di- and tetrahydropyrroles: III. Reaction of methyl α-methoxycarbonyl-β, β-dimethyl-γ-nitrobutyrate with methyl acrylate under the conditions of the Michael reaction
13. Spectrophotometric control of the intermediates in the synthesis of pteroylglutamic (folic) acid: III. Determination of 2,4-diamino-6-hydroxypyrimidine and 2,4,5-triamino-6-hydroxypyrimidine sulfate
14. Investigations on derivatives of 5′-O-tosyladenosine
15. Spectrophotometric determination of p-nitrobenzoyl chloride, p-nitrobenzoyl-L-glutamic acid, and p-aminobenzoyl-L-glutamic acid
16. Spectrophotometric determination of 2,4-diamino-6-hydroxy-5-isonitrosopyrimidine
17. Quantitative determination of 2-butyne-1,4 diol in industrial aqueous solutions
18. Differential spectrophotometric determination of thiamine bromide
19. METHOD OF CREATING P-N TRANSFERS
20. METHOD OF CREATING P-N TRANSFERS
21. ChemInform Abstract: DIE SUCHE NACH EINFACHEN CHEMISCHEN MODELLEN DES COBAMIDCOFERMENTES 3. MITT. DIE SYNTHESE VON BETA‐HYDROXY‐ UND BETA‐ALKOXYMETHYLVINYLCOBALOXIMEN
22. ChemInform Abstract: DIE SUCHE NACH EINFACHEN CHEMISCHEN MODELLEN DES COBAMIDCOFERMENTS 4. MITT. ALKOHOLYSE UND ACIDOLYSE VON BETA‐HYDROXYALKYL‐(PYRIDIN)‐COBALOXIMEN
23. ChemInform Abstract: POLYEN‐SYNTH. 35. MITT. ISOMERIE VON 6,10‐DIMETHYL‐UNDECATRIEN‐(3,5,9)‐ON‐(2) (PSEUDOJONON)
24. Preparation of polymeric materials with semiconductor properties
25. ChemInform Abstract: AENDERUNG DER SELEKTIVEN WIRKUNG VON KATALYSATOREN BEI DER HYDRIERUNG DES DIENSYST. 7. MITT. MODIFIZIERUNG VON NICKEL-KATALYSATOREN DURCH BLEI
26. ChemInform Abstract: UNTERSUCHUNG DER INVERSION VON 4‐BENZOYLAMINO‐3‐HYDROXYTHIOPHAN
27. ChemInform Abstract: DIE SYNTHESE VON DI‐ UND TETRAHYDROPYRROLEN 8. MITT. SYNTHESE UND EIGENSCHAFTEN DES 2,3,3‐TRIMETHYL‐2‐HYDROXYPYRROLIDONS‐(5)
28. ChemInform Abstract: DIE SYNTH. ALLER MOEGLICHEN STEREOISOMEREN DES 4‐BENZOYLAMINO‐3‐HYDROXY‐2‐(DELTA‐METHOXYCARBONYLBUTYL)‐THIOPHANS
29. Synthesis of all of the possible stereoisomers of 4-benzamido-3-hydroxy-2-(?-carbomethoxybutyl)thiophan
30. ChemInform Abstract: DIE SYNTHESE DES PHYTYLUBICHINONS UND SEINER ANALOGEN, ELEKTROPHILE SUBSTITUTION DER METHOXYGRUPPE IN DER UBICHINONREIHE
31. ChemInform Abstract: MECHANISMUS DER KATALYTISCHEN HYDRIERUNG ALPHA,BETA‐UNGESAETTIGTER KETONE
32. ChemInform Abstract: NMR‐SPEKTREN DER CIS‐ UND TRANS‐ISOMEREN DES 4‐AMINO‐3‐HYDROXYTHIOPHANS
33. ChemInform Abstract: SYNTH. VON POLYENVERBINDUNGEN 33. MITT. DARST. UND UMLAGERUNG VON ACETON-(3-METHYL-PENTAN-(1)-IN-(4)-YL-(3))-METHYLKETAL
34. ChemInform Abstract: UNTERSUCHUNG DER STRUKTUR UND DER INVERSION DES 4-BENZYLAMINO-TRANS-3-HYDROXY-TRANS-2-CARBOMETHOXYTHIOPHANS
35. ChemInform Abstract: SYNTH., AUFBAU UND RK. VON DI‐ UND TETRAHYDROPYRROLEN 7. MITT. DIE IMINO‐ENAMIN‐TAUTOMERIE VON PYRROLINEN IN LOESUNGEN
36. The use of synthetic inhibitors to study the interaction of nicotinamide adenine dinucleotide with yeast alcohol dehydrogenase.
37. [Physicochemical properties and quantitative determination of bromacetopropylacetate].
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