These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
232 related articles for article (PubMed ID: 5975206)
21. Compounds related to the steroid hormones. 18. Reaction of 16-alpha,17-alpha-epoxy-16-beta-methyl-5-alpha-pregnan-20-ones with boron trifluoride. May PJ; Nice FA; Phillipps GH J Chem Soc Perkin 1; 1966; 23():2210-7. PubMed ID: 5951101 [No Abstract] [Full Text] [Related]
22. ACID-CATALYZED REARRANGEMENT OF 20-ALPHA-ETHYNYLPREGN-5-ENE-3-BETA, 20-BETA-DIOL 3-ACETATE. CHAUDHURI NK; GUT M J Am Chem Soc; 1965 Aug; 87():3737-44. PubMed ID: 14340661 [No Abstract] [Full Text] [Related]
23. Synthesis of 6-chloro-16-methylene-17-alpha-- hydroxy-21-fluoro-4,6-pregnadiene-3,20-dione 17-acetate, a potent progestational agent. Popper TL; Carlon FE; Shapiro EL; Neri R J Med Chem; 1971 Jan; 14(1):33-5. PubMed ID: 5539741 [No Abstract] [Full Text] [Related]
24. Isolation and identification of 3-alpha,21-dihydroxy-5-alpha-pregnane-11,20-dione from urine. Starnes WR; Partlow TF Anal Biochem; 1965 Jul; 12(1):157-62. PubMed ID: 5850398 [No Abstract] [Full Text] [Related]
25. Structural requirements for the action of steroids as quenchers of albumin fluorescence. Romeu AM; Martino EE; Stoppani AO Biochim Biophys Acta; 1975 Dec; 409(3):376-86. PubMed ID: 1239298 [TBL] [Abstract][Full Text] [Related]
26. The synthesis of steroidal 1-beta, 2-beta-methylene derivatives. Tanabe M; Crowe DF Tetrahedron; 1967 May; 23(5):2115-21. PubMed ID: 6044196 [No Abstract] [Full Text] [Related]
34. Plasma progestagens in the mare, fetus and newborn foal. Holtan DW; Houghton E; Silver M; Fowden AL; Ousey J; Rossdale PD J Reprod Fertil Suppl; 1991; 44():517-28. PubMed ID: 1795295 [TBL] [Abstract][Full Text] [Related]
35. The preparation of alpha-phenylketo steroids. Poletto JF; Allen GR; Weiss MJ J Med Chem; 1967 Jan; 10(1):106-8. PubMed ID: 6031684 [No Abstract] [Full Text] [Related]
36. Compounds related to the steroid hormones. XVII. An improved method of preparation of 21-acetoxy-17-hydroxy-16-beta-methyl-5-alpha-pregn-9-ene-3,20-dione. Gregory GI; Hunt JS; May PJ; Nice FA; Phillipps GH J Chem Soc Perkin 1; 1966; 23():2201-10. PubMed ID: 5951100 [No Abstract] [Full Text] [Related]
37. Steroids and related products. XLII. (1) The synthesis of 11-oxa steroids. IV. (2) The synthesis of 17,21-dihydroxy-11-oxa-4-pregene-3,20-dione, an 11-oxa analogue of the 17-hydroxylated glucocorticoids. Salvi VS; Mukherjee D; Chowdhurry NM; Engel CR Steroids; 1976 May; 27(5):717-25. PubMed ID: 941188 [TBL] [Abstract][Full Text] [Related]
38. The absolute configuration at C-20 in 11-oxo-3,20,21-trihydroxy steroids. Mattox VR; Vrieze W J Org Chem; 1967 Mar; 32(3):708-13. PubMed ID: 6042120 [No Abstract] [Full Text] [Related]
39. Pinacol type rearrangements in the D ring of steroids. Ghera E Tetrahedron Lett; 1967 Jan; 1():17-21. PubMed ID: 6044784 [No Abstract] [Full Text] [Related]