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16-Beta-hydroxymethyl- and 16-beta-formyl-D-nor-4-androsten-3-one. 1966

H Reimann, and O Z Sarre, and E P Oliveto

UI MeSH Term Description Entries
D002625 Chemistry, Organic The study of the structure, preparation, properties, and reactions of carbon compounds. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed) Organic Chemistry
D013256 Steroids A group of polycyclic compounds closely related biochemically to TERPENES. They include cholesterol, numerous hormones, precursors of certain vitamins, bile acids, alcohols (STEROLS), and certain natural drugs and poisons. Steroids have a common nucleus, a fused, reduced 17-carbon atom ring system, cyclopentanoperhydrophenanthrene. Most steroids also have two methyl groups and an aliphatic side-chain attached to the nucleus. (From Hawley's Condensed Chemical Dictionary, 11th ed) Steroid,Catatoxic Steroids,Steroids, Catatoxic
D055601 Organic Chemistry Phenomena The conformation, properties, reaction processes, and the properties of the reactions of organic carbon compounds. Organic Chemistry Concepts,Organic Chemistry Processes,Organic Chemistry Phenomenon,Organic Chemistry Process,Chemistry Process, Organic,Chemistry Processes, Organic,Concept, Organic Chemistry,Concepts, Organic Chemistry,Organic Chemistry Concept,Phenomena, Organic Chemistry,Phenomenon, Organic Chemistry,Process, Organic Chemistry,Processes, Organic Chemistry

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H Reimann, and O Z Sarre, and E P Oliveto
[17-beta-hydroxymethyl-steroids: presentation of derivatives of 17-Beta-hydroxymethyl-4-androsten-3-ones].
December 1965, Experientia,
H Reimann, and O Z Sarre, and E P Oliveto
[17-Beta-hydroxymethyl-steroid: presentation of 17-alpha-hydroxy-17-beta-hydroxymethyl-4-androsten-3-one from Reichstein's substance S].
September 1965, Experientia,
H Reimann, and O Z Sarre, and E P Oliveto
[17-Beta-hydroxymethyl-steroids: presentation of derivatives of 17-alpha-hydroxy-17-beta-hydroxymethyl-4-androsten-3-ones].
October 1965, Experientia,
H Reimann, and O Z Sarre, and E P Oliveto
17-beta-(4'-(p-[bis(beta-chloroethyl)amino]phenyl)-butanoyloxy)-4-androsten-3-one.
September 1968, Journal of medicinal chemistry,
H Reimann, and O Z Sarre, and E P Oliveto
Synthesis of 16 alpha,19-dihydroxy-4-androstene-3,17-dione and 3 beta,16 alpha,19-trihydroxy-5-androsten-17-one and their 17 beta-hydroxy-16-keto isomers.
January 1987, Steroids,
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The metabolism in man of (3H)-5alpha-16-androsten-3alpha-ol and of (3H)-5alpha-16-androsten-3-one.
January 1978, Hormone research,
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Conversion of androstenedione to 3 beta-hydroxy-5-androsten-17-one and 3 beta-hydroxy-4-androsten-17-one by the testicular microsomal fraction of Sprague-Dawley rats.
April 1987, Journal of biochemistry,
H Reimann, and O Z Sarre, and E P Oliveto
Biosynthesis of 16 alpha, 17 alpha-epoxy-4-androsten-3-one in rat liver microsomes.
September 1980, Acta endocrinologica,
H Reimann, and O Z Sarre, and E P Oliveto
Studies on steroids. XIX. 16-Methylenamine of delta 5-androsten-3-beta-olo-17-one.
March 1969, Il Farmaco; edizione scientifica,
H Reimann, and O Z Sarre, and E P Oliveto
Intramolecular cyclization of 3-beta-acetoxy-16-picolinylidene-5-androsten-17-one by catalytic hydrogenation.
June 1970, Tetrahedron,
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