[go: up one dir, main page]

Barber et al., 1955 - Google Patents

INVESTIGATIONS ON STEROIDS. XXV. 19-OXOPROGESTERONE AND 19-OXO-11-DESOXYCORTICOSTERONE*, 1

Barber et al., 1955

Document ID
3659223905046550817
Author
Barber G
EHRENSTEIN M
Publication year
Publication venue
The Journal of Organic Chemistry

External Links

Snippet

The synthesis, starting from strophanthidin, of 19-hydroxyprogesterone (III) and 19-hydroxy- 11-desoxycorticosterone (VII) has been described (1, 2) and the spatial similarity of VII to corticosterone has been pointed out (2). The present paper is concerned with the extension …
Continue reading at pubs.acs.org (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J75/00Processes for the preparation of steroids in general
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J71/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
    • C07J71/0005Oxygen-containing hetero ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J71/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
    • C07J71/0036Nitrogen-containing hetero ring
    • C07J71/0042Nitrogen only
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J1/00Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
    • C07J1/0003Androstane derivatives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J7/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
    • C07J7/0005Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21
    • C07J7/001Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group
    • C07J7/0015Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group not substituted in position 17 alfa
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J13/00Normal steroids containing carbon, hydrogen, halogen or oxygen having a carbon-to-carbon double bond from or to position 17
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J41/00Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
    • C07J41/0033Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J5/00Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J9/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane

Similar Documents

Publication Publication Date Title
Djerassi et al. Steroids. LIV. 1 Synthesis of 19-Nov-17α-ethynyltestosterone and 19-Nor-17α-methyltestosterone2
Fukushima et al. The characterization of four new metabolites of adrenocortical hormones
Marshall et al. 7-Keto Steroids. II. 1 Steroidal 3β-Hydroxy-Δ5-7-ones and Δ3, 5-7-Ones
Bloch et al. Ci, STEROIDS, 17a-HYDROXYCORTICOSTERONE AND A SODIUM RETAINING FACTOR IN HUMAN FETAL ADRENAL GLANDS
Buchi et al. Synthesis of patchouli alcohol
Djerassi et al. Steroids. XLVIII. 1 19-Norprogesterone, a Potent Progestational Hormone
Barber et al. INVESTIGATIONS ON STEROIDS. XXV. 19-OXOPROGESTERONE AND 19-OXO-11-DESOXYCORTICOSTERONE*, 1
Stavely Molecular Rearrangements of 17-Hydroxy-pregnane Compounds1
Meyer et al. The conversion of Δ4-androstene-3, 17-dione-4-C14 and dehydroepiandrosterone by bovine adrenal homogenate preparations
Woodward et al. The total synthesis of cholesterol
Jones et al. Studies in steroid metabolism. VI. The characterization of 11-and 12-oxygenated steroids by infrared spectrometry
US2759951A (en) Cyclopentanophenanthrene derivatives and compounds
US2840581A (en) Carbonyloxy steroids
Knight et al. The Structure of the cactus sterol macdougallin (14α-Methyl-Δ8-cholestene-3β, 6α-diol). A novel link in sterol biogenesis1, 2
EHRENSTEIN et al. Investigations on Steroids. XXX. New Transformation Products of Strophanthidin: 19-Hydroxytestosterone, 19-Hydroxy-1-dehydrotestosterone Diacetate and Estradiol-17β1-3
Ringold et al. Steroids. LXXV. Dehydrogenation of testosterone to Δ1, 4-androstadien-17β-ol-3-one with selenium dioxide
Dale et al. Isolation and identification of 16α, 18-dihydroxydeoxycorticosterone from human adrenal gland incubations
Engel et al. Steroids and related products. III. The synthesis of 17β-methyl-17-isodesoxycorticosterone
EHRENSTEIN et al. Investigations on Steroids. XXVI. Synthesis of 19-Hydroxy-▵ 4-androstene-3, 17-dione1, 2
Bots Investigations on sterols XI: Preparation of 13α‐androstene derivatives
Bernstein et al. Steroidal Cyclic Ketals. VIII. 1▵ 4, 9 (11)-Pregnadi ene-17α, 21-diol-3, 20-dione
Hirschmann et al. A SYNTHESIS OF 16α-HYDROXY-20-KETOSTEROIDS AND THEIR CORRELATION WITH OTHER RING D SUBSTITUTED STEROIDS. THE CONFIGURATION OF THE SAPOGENIN SIDE CHAIN1, 2
Caspi et al. Reaction of lead tetraacetate with steroidal α, α′-dihydroxy ketones in alcoholic media
Francois et al. In vitro metabolism of progesterone-4-14C by the adrenal gland of the Mongolian gerbil
Idler et al. Isolation of 20β-dihydrocortisone from sockeye salmon (Oncorhynchus nerka) plasma