49 results on '"Deak A"'
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2. ChemInform Abstract: Synthesis of 1-Aryl-1,4-dihydro-3(2H)-isoquinolinones with Piperazine Ring in the Side Chain Having Potential Antiserotoninergic Activity
3. ChemInform Abstract: Synthesis of 5,6,7,8-Tetrahydro-3-isoquinolylamines
4. ChemInform Abstract: Cyclization of N-(2-Aminobenzyl) Benzylamino-1-phenyl-1-ethanols and Debenzylation of the Resulting Tetrahydroisoquinoline Derivatives
5. ChemInform Abstract: Condensed Heterocyclic Lactams. Part 1. Study on the Cyclization Methods Resulting in 4-Aryl-3,4-dihydroquinolin-2(1H)-ones
6. ChemInform Abstract: Condensed Heterocyclic Lactams. Part 2. Synthesis of New 4- Arylquinolin-2(1H)-one Derivatives
7. ChemInform Abstract: Steric and Electronic Tuning of Atropisomeric Amino Alcohol Type Ligands with a 1-Arylpyrrole Backbone.
8. ChemInform Abstract: New Approach to Bicyclo [5.3.0] Ring Systems
9. ChemInform Abstract: A New Pyrrolidine-Derived Atropisomeric Amino Alcohol as a Highly Efficient Chiral Ligand for the Asymmetric Addition of Diethylzinc to Aldehydes.
10. ChemInform Abstract: Stimuli-Responsive Dynamic Gold Complexes
11. ChemInform Abstract: Cyclization of N-(2-Aminobenzyl) Benzylamino-1-phenyl-1-ethanols and Debenzylation of the Resulting Tetrahydroisoquinoline Derivatives.
12. ChemInform Abstract: Synthesis of 5,6,7,8-Tetrahydro-3-isoquinolylamines.
13. ChemInform Abstract: Synthesis of 1-Aryl-1,4-dihydro-3(2H)-isoquinolinones with Piperazine Ring in the Side Chain Having Potential Antiserotoninergic Activity.
14. ChemInform Abstract: Condensed Heterocyclic Lactams. Part 1. Study on the Cyclization Methods Resulting in 4-Aryl-3,4-dihydroquinolin-2(1H)-ones.
15. ChemInform Abstract: New Approach to Bicyclo [5.3.0] Ring Systems.
16. ChemInform Abstract: UV Spectra of 3(2H)-Isoquinolinones and Their Saturated Derivatives
17. ChemInform Abstract: Synthesis of New 4-Aryl-8-heteroaryl-2-methyl-1,2,3,4-tetrahydroisoquinolines
18. ChemInform Abstract: 8-Amino-4-aryl-2-methyl-1,2,3,4-tetrahydroisoquinolines: Reactions of the Amino Group via the Diazonium Salts. Synthesis and Biological Activity of Novel 8-Substituted 4-Aryl-2-methyltetrahydroisoquinolines
19. ChemInform Abstract: Diels-Alder Reactions of Isoquinolin-3(2H)-ones. Part 6. An Unusual Diels-Alder Reaction of 4-Benzyl-1-phenylbenzo(g)isoquinolin-3-ol with N-Phenylmaleimide
20. Organotin(IV)n+ Complexes Formed with Biologically Active Ligands
21. ChemInform Abstract: Novel Synthesis and Crystal Structure of 1,4‐Bis(3‐chloro‐1,1,3‐trimethylbutyl)benzene.
22. ChemInform Abstract: Condensed Heterocyclic Lactams. Part 2. Synthesis of New 4‐ Arylquinolin‐2(1H)‐one Derivatives.
23. ChemInform Abstract: UV Spectra of 3(2H)-Isoquinolinones and Their Saturated Derivatives
24. ChemInform Abstract: Synthesis of New 4-Aryl-8-heteroaryl-2-methyl-1,2,3,4-tetrahydroisoquinolines.
25. ChemInform Abstract: 8-Amino-4-aryl-2-methyl-1,2,3,4-tetrahydroisoquinolines: Reactions of the Amino Group via the Diazonium Salts. Synthesis and Biological Activity of Novel 8-Substituted 4-Aryl-2-methyltetrahydroisoquinolines.
26. ChemInform Abstract: Diels‐Alder Reactions of Isoquinolin‐3(2H)‐ones. Part 6. An Unusual Diels‐Alder Reaction of 4‐Benzyl‐1‐phenylbenzo(g)isoquinolin‐3‐ol with N‐Phenylmaleimide.
27. ChemInform Abstract: Hydroxyiminoisoquinolin-3(2H)-ones. Part 8. Acid-Catalyzed Ring Contraction and Semmler-Wolff Type Rearrangement
28. ChemInform Abstract: Hydroxyiminoisoquinolin-3(2H)-ones. Part 7. Rearrangement of 4-Hydroxyimino-1,4-dihydroisoquinolin-3(2H)-ones Under Wolff-Semmler-Type Reaction Conditions
29. ChemInform Abstract: Hydrogenation of 3(2H)-Isoquinolinones and the Stereochemistry of the Products
30. ChemInform Abstract: Hydroxyiminoisoquinolin-3(2H)-ones. Part 5. Synthesis of 4-Amino-1,2,3,4-tetrahydroisoquinolines
31. ChemInform Abstract: Hydroxyiminoisoquinolin-3(2H)-ones. Part 9. Synthesis of Some Oxazolo-(5,4-c)-, Thiazolo(5,4-c)-, and 2,3-Dihydro-1H-(1,4)oxazino(2,3-c)isoquinolines
32. ChemInform Abstract: Hydrogenation of Substituted 1-Arylisoquinolin-3(2H)-ones to 5,6,7,8-Tetrahydro- and 1,4-Dihydroisoquinolin-3(2H)-ones
33. ChemInform Abstract: Lithiation of 1-Aryl-1,4-dihydro-3(2H)-isoquinolinones and Their N-Methyl Derivatives
34. ChemInform Abstract: Synthesis and Cyclization of Bis-amides into Isoquinolinones
35. ChemInform Abstract: Hydroxyiminoisoquinolin-3(2H)-ones. Part 8. Acid-Catalyzed Ring Contraction and Semmler-Wolff Type Rearrangement.
36. ChemInform Abstract: Hydroxyiminoisoquinolin-3(2H)-ones. Part 9. Synthesis of Some Oxazolo-(5,4-c)-, Thiazolo(5,4-c)-, and 2,3-Dihydro-1H-(1,4)oxazino(2,3-c)isoquinolines.
37. ChemInform Abstract: Hydroxyiminoisoquinolin-3(2H)-ones. Part 5. Synthesis of 4-Amino-1,2,3,4-tetrahydroisoquinolines.
38. ChemInform Abstract: Hydrogenation of 3(2H)-Isoquinolinones and the Stereochemistry of the Products.
39. ChemInform Abstract: Lithiation of 1-Aryl-1,4-dihydro-3(2H)-isoquinolinones and Their N-Methyl Derivatives.
40. ChemInform Abstract: Synthesis and Cyclization of Bis-amides into Isoquinolinones.
41. ChemInform Abstract: Hydroxyiminoisoquinolin‐3(2H)‐ones. Part 7. Rearrangement of 4‐Hydroxyimino‐1,4‐dihydroisoquinolin‐3(2H)‐ones Under Wolff‐Semmler‐Type Reaction Conditions.
42. ChemInform Abstract: Hydrogenation of Substituted 1-Arylisoquinolin-3(2H)-ones to 5,6,7,8-Tetrahydro- and 1,4-Dihydroisoquinolin-3(2H)-ones.
43. Organotin(IV)n+ Complexes Formed with Biologically Active Ligands.
44. ChemInform Abstract: New Approach to Bicyclo [5.3.0] Ring Systems.
45. ChemInform Abstract: Condensed Heterocyclic Lactams. Part 1. Study on the Cyclization Methods Resulting in 4-Aryl-3,4-dihydroquinolin-2(1H)-ones.
46. ChemInform Abstract: Cyclization of N-(2-Aminobenzyl) Benzylamino-1-phenyl-1-ethanols and Debenzylation of the Resulting Tetrahydroisoquinoline Derivatives.
47. ChemInform Abstract: Synthesis of 1-Aryl-1,4-dihydro-3(2H)-isoquinolinones with Piperazine Ring in the Side Chain Having Potential Antiserotoninergic Activity.
48. ChemInform Abstract: Synthesis of 5,6,7,8-Tetrahydro-3-isoquinolylamines.
49. Organotin(IV)n+Complexes Formed with Biologically Active Ligands
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