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Journal Abstract Search
153 related items for PubMed ID: 5085129
1. Characterisation of the products from the dehydration of steroidal 4xi, 5xi-dihydroxy-3,6-diketone systems. Tait AD. Steroids; 1972 Oct; 20(4):417-34. PubMed ID: 5085129 [No Abstract] [Full Text] [Related]
2. Preparation of 7-chloro steroids. Guthrie RW, Boris A, Mennona FA, Mullin JG, Kierstead RW. J Med Chem; 1973 Jan; 16(1):65-8. PubMed ID: 4682203 [No Abstract] [Full Text] [Related]
3. Aromatization of some 4,5-epoxy-3-hydroxysteroids. Baldwin D, Hanson JR. J Chem Soc Perkin 1; 1972 Jan; 15():1889-91. PubMed ID: 4672377 [No Abstract] [Full Text] [Related]
4. Characterization of the products from the oxidation of progesterone with osmium tetroxide. Tait AD. Steroids; 1972 Nov; 20(5):531-42. PubMed ID: 4654973 [No Abstract] [Full Text] [Related]
11. Synthesis of (4- 14 C)-labeled and non-labeled 3 , 15 -dihydroxy-5-pregnen-20-one and 3 , 15 -dihydroxy-5-androsten-17-one. Bhavnani BR, Stanczyk FZ. Steroids; 1972 Aug 11; 20(2):129-42. PubMed ID: 5078257 [No Abstract] [Full Text] [Related]
12. Steroids and related products. 39. The functionalization of the 17-methyl group of 17 -methyl steroids. II. The synthesis of 12 ,17 1 -epoxy-17 -methylprogesterone and of 20-oxygenated 17 -hydroxymethyl steroids. Engel CR, Mukherjee D, Beaudoin GJ. Steroids; 1973 Jun 11; 21(6):857-75. PubMed ID: 4716629 [No Abstract] [Full Text] [Related]
13. Synthesis of steroids containing the -keto acid side-chain. Monder C. Steroids; 1971 Aug 11; 18(2):187-94. PubMed ID: 4331314 [No Abstract] [Full Text] [Related]
14. 17 -Hydroperoxypregnenes. IV. A comparative study of the fragmentation by electron impact and high temperature chromatography. Tan L, Wang HM, Falardeau P. Can J Biochem; 1972 Jun 11; 50(6):706-9. PubMed ID: 5042878 [No Abstract] [Full Text] [Related]
15. Hydroxy-steroids. XVII. The 5 -androstane-16,17-diols and related compounds. Combe MG, Denny WA, Meakins GD, Morisawa Y, Richards EE. J Chem Soc Perkin 1; 1971 Jun 11; 12():2300-5. PubMed ID: 5170059 [No Abstract] [Full Text] [Related]
16. Studies in in the steroid group. LXXXII. The preparation of nine mono- and eight di-oxoandrostanes, 5 -estran-17-one, and 5 -pregnane-2,20-dione. Clegg AS, Denny WA, Jones ER, Kumar V, Meakins GD, Thomas VE. J Chem Soc Perkin 1; 1972 Jun 11; 4():492-8. PubMed ID: 5066074 [No Abstract] [Full Text] [Related]