63 results on '"Emanuel B Hershberg"'
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2. 11-Oxygenated Steroids. XVIII. Wagner-Meerwein Rearrangement of Some 17α-Hydroxysteroids*
3. 11-Oxygenated Steroids. II. The Reduction of 11-Carbonyl to 11α-Hydroxyl in the Etiocholane Series
4. Wagner-Meerwein Rearrangements. III. Further Aspects of Acid-catalyzed Opening of Steroidal 16,17-Epoxides
5. Long-acting Testosterone Esters. Some Considerations on their Biological Utilization1
6. 11-Amino-Steroids. III. 11-Acetamido Derivatives of Cortexolone1-3
7. Wagner-Meerwein Rearrangements. II. Acid-catalyzed Opening of Steroidal 16,17-Epoxides
8. Catalytic Isomerization of Spirostans to Furostenols1
9. The Dienol-Benzene Rearrangement.1 Some Chemistry of 1,4-Androstadiene-3,17-dione
10. 11-Amino Steroids. II. 11-Amino- and 11-Acetamido-3,20-dioxypregnanes1
11. 16-Alkylated Corticoids. IV.1 Synthesis of 16β-Methyl Analogs of Cortisone, Prednisone, and 9α-Fluoroprednisolone2
12. 11-Oxygenated Steroids. XII. The Preparation of 17α-Hydroxycorticosterone 21-Acetate (Kendall's Compound F Acetate) via 11β-Formates1
13. Synthesis of 17α-Halo Analogs of Corticoids. 17α-Chloro- and 17α-Fluoro-4-pregnen-21-ol-3,11,20-trione Acetates
14. Selective Reduction and Hydrogenation of Unsaturated Steroids1
15. 11-Oxygenated Steroids. XI. The Synthesis of 17α-Hydroxycorticosterone (Compound F) 21-Acetate from Pregnane-11β,17α-diol-3,20-dione
16. Some Substances Derived from Ruscogenin
17. The Formation of Ketals from Steroid Ketones with Selenium Dioxide and Methanol
18. Simultaneous Oxidation and Bromination of 21-Acetoxypregnan-3α,17α-diol-11,20-dione
19. Notes. Microbiological Transformation of Steroids. VII. 15β-Hydroxylation
20. 11-Oxygenated Steroids. VII. The Acylation of 11β-Hydroxy Steroids: The Synthesis of Compound F 11-Acetate and Related Compounds1
21. Steroidal Amines. III. 16α-Amino-Substituted Pregnanes1
22. 11-Oxygenated Steroids. I. Partial Syntheses of 11-Ketotestosterone and of Adrenosterone
23. Weak Acid-catalyzed Rearrangement of the Dihydroxyacetone Side Chain in Steroids
24. Some Transformation Products of Cortisone Acetate
25. 11-Oxygenated Steroids. III. The Preparation of 11β-Hydroxy Pregnanes1
26. Transformation Products of Strophanthidin. I. The Preparation of 14β,19-Dihydroxydesoxycorticosterone 19,21-Diacetate
27. 11-Oxygenated Steroids. VIII. The Synthesis of 16,17-Oxido-4-pregnen-11α-ol-3,20-one Acetate
28. D-Homo Rearrangement of 11-Oxygenated 17α-Hydroxy-20-ketosteroids
29. 11-Oxygenated Steroids. VI. The Synthesis of Δ4-Pregnen-11α,17α-diol-3,20-dione (11α, 17α-Dihydroxyprogesterone) and Δ4-Pregnen-11α,17α,21-triol-3,20-dione 11-Acetate (11-Epi-Compound F 11-Acetate)1,2
30. 11-Oxygenated Steroids. V. The Preparation of 11α-Hydroxypregnanes1
31. Allopregnan-17 α,21-diol-3,11,20-trione-21-acetate
32. 11-Oxygenated Steroids. IV. The Selective Reduction of Steroidal 11,20-Diketones with Sodium Borohydride1
33. Cyclic Ketals of 4-Androstene-3,17-dione
34. Notes - Attempts to Prepare New Progestational Agents: Synthesis and Biological Activity of 11β-Acyloxyprogesterones
35. 11-Oxygenated Steroids. XIV. New Syntheses of Corticosterone1
36. 11-Oxygenated Steroids. XVI. The Preparation of Hydrocortisone from Cortisone Acetate1
37. A new synthesis of Kendall's compound F
38. The acylation of 11 beta-hydroxy steroids; the synthesis of delta4-pregnen-11beta, 17alpha, 21-triol-3, 20-dione 11, 21-diacetate (compound F 11, 21-diacetate)
39. Catalytic Hydrogenation of Cholesterol
40. Transformation Products of Strophanthidin. II. Some 10-Cyano Derivatives1
41. 11-Oxygenated Steroids. X. The Reduction of 21-Benzylidenepregnan-3α-ol-11,20-dione with Various Metal Hydrides1
42. MICROBIOLOGICAL TRANSFORMATION OF STEROIDS. 2β-HYDROXYLATION
43. Notes - Microbiological Transformation of Steroids. V. Action of Several Bacterial Species on 4-Pregnene-17α,21-diol-3,20-dione
44. Some Glyoxylic Steroids
45. The Preparation of 17α-Hydroxy-20-ketosteroids
46. 11-Oxygenated Steroids. IX. The Elimination of the 11α-Hydroxyl Group via the Tosylate
47. Notes - Synthesis of 11β-Acetoxytestosterone Acetate
48. Reduction Studies on Unsaturated Steroids
49. A Precision Melting Point Apparatus
50. α-Reduction of a Steroidal Δ16-20-Ketone with Lithium Aluminum Hydride
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