BIOMAT Database Logo BIOMAT Database Logo

Steroids. XVII. Functionalisation of the 5 beta-methyl group in 9,10-epoxy-5-methyl-19-nor 5 beta-steroids and 5-methyl-18,19-bisnor-delta 13(17)-5 beta, 8 alpha, 9 beta, 10 alpha, 14 beta-steroids. 1973

J Gareth, and L I Jones, and B A Marples

UI MeSH Term Description Entries
D009654 Norsteroids Steroids which have undergone contraction in ring size or reduction in side chains.
D002776 Cholestanes Derivatives of the saturated steroid cholestane with methyl groups at C-18 and C-19 and an iso-octyl side chain at C-17.
D004988 Ethers, Cyclic Compounds of the general formula R-O-R arranged in a ring or crown formation. Cyclic Ether,Cyclic Ethers,Ether, Cyclic

Related Publications

J Gareth, and L I Jones, and B A Marples
14 Alpha, 17 alpha-alkylidenedioxy steroids. 2. 19-Nor-9 alpha, 10 beta- and 19-nor-9 beta, 10 alpha-progesterone analogs.
November 1973, Journal of medicinal chemistry,
J Gareth, and L I Jones, and B A Marples
14Alpha, 17 alpha-alkylidenedioxy steroids. 2. 19-Nor-9 alpha, 10 beta- and 19-nor-9 beta, 10 alpha-progesterone analogs.
November 1973, Journal of medicinal chemistry,
J Gareth, and L I Jones, and B A Marples
[Investigation of steroids. XLII. Transformation of 17-alpha-pseudostrophanthidins to 19-hydroxy-8,19-epoxy-14-beta,17-alpha-cortexone and 8-hydroxy-19-nor-14-beta,17-alpha-cortexone].
January 1969, Helvetica chimica acta,
J Gareth, and L I Jones, and B A Marples
Steroids. XV. Rearrangements of 9- and 10-hydroxy-5 -methyl-19-nor-steroids.
January 1972, Journal of the Chemical Society. Perkin transactions 1,
J Gareth, and L I Jones, and B A Marples
Non-natural 14-hydroxy steroids. II. 13 alpha,14 alpha and 13 beta,14 beta isomers of methyl 14-hydroxy-1,7,17-trioxo-5 beta-androst-8-ene-19-oate.
August 1991, Acta crystallographica. Section C, Crystal structure communications,
J Gareth, and L I Jones, and B A Marples
Heterocyclic steroids. 13. The synthesis of N-methyl-6-aza-8(14)-dehydro-19-nor-testosterone.
September 1968, Tetrahedron,
J Gareth, and L I Jones, and B A Marples
A comparative study of the metabolic fate of testosterone, 17 alpha-methyl-testosterone. 19-nor-testosterone. 17 alpha-methyl-19-nor-testosterone and 17 alpha-methylestr-5(10)-ene-17 beta-ol-3-one in normal males.
January 1961, Clinica chimica acta; international journal of clinical chemistry,
J Gareth, and L I Jones, and B A Marples
[19-nor-5-beta-Methyl steroids. 3. Acetolysis of 3-methoxy steroids].
July 1965, Justus Liebigs Annalen der Chemie,
J Gareth, and L I Jones, and B A Marples
[Antiprogestational steroids: synthesis of 7 alpha- and 7 beta-methyl-a-nor-5 alpha-androstane-2 alpha, 17 alpha-DI-ethynyl-2 beta,17 beta-diol].
September 1986, Yao xue xue bao = Acta pharmaceutica Sinica,
J Gareth, and L I Jones, and B A Marples
Steroids and related products. XXVI. The functionalization of the 17-methyl group of 17-alpha,17-1-epoxy-17-alpha-methylprogesterone.
February 1968, Tetrahedron letters,
Copied contents to your clipboard!