Magyar et al., 2004 - Google Patents
Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and D-homosteroids by intramolecular cyclization reactionsMagyar et al., 2004
- Document ID
- 5293214018071319059
- Author
- Magyar A
- Wölfling J
- Kubas M
- Seijo J
- Sevvana M
- Herbst-Irmer R
- Forgó P
- Schneider G
- Publication year
- Publication venue
- Steroids
External Links
Snippet
Steroidal aryliminium salts were prepared from d-seco-pregnene aldehyde 2b, and their BF3· OEt2-catalyzed reactions were studied. The nature of the substituent R1 in the anilines 3–6 essentially influenced the chemoselectivity. Using unsubstituted 3, 4-methoxy-(4) or 4 …
- 230000015572 biosynthetic process 0 title description 14
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
- C07J71/0005—Oxygen-containing hetero ring
- C07J71/001—Oxiranes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J7/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
- C07J7/0005—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0003—Androstane derivatives
- C07J1/0018—Androstane derivatives substituted in position 17 beta, not substituted in position 17 alfa
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
- C07J71/0036—Nitrogen-containing hetero ring
- C07J71/0042—Nitrogen only
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J53/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by condensation with a carbocyclic rings or by formation of an additional ring by means of a direct link between two ring carbon atoms, including carboxyclic rings fused to the cyclopenta(a)hydrophenanthrene skeleton are included in this class
- C07J53/002—Carbocyclic rings fused
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J13/00—Normal steroids containing carbon, hydrogen, halogen or oxygen having a carbon-to-carbon double bond from or to position 17
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J63/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by expansion of only one ring by one or two atoms
- C07J63/008—Expansion of ring D by one atom, e.g. D homo steroids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J43/00—Normal steroids having a nitrogen-containing hetero ring spiro-condensed or not condensed with the cyclopenta(a)hydrophenanthrene skeleton
- C07J43/003—Normal steroids having a nitrogen-containing hetero ring spiro-condensed or not condensed with the cyclopenta(a)hydrophenanthrene skeleton not condensed
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J31/00—Normal steroids containing one or more sulfur atoms not belonging to a hetero ring
- C07J31/006—Normal steroids containing one or more sulfur atoms not belonging to a hetero ring not covered by C07J31/003
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J9/00—Normal 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
- C07J9/005—Normal 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 containing a carboxylic function directly attached or attached by a chain containing only carbon atoms to the cyclopenta[a]hydrophenanthrene skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J17/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, having an oxygen-containing hetero ring not condensed with the cyclopenta(a)hydrophenanthrene skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J75/00—Processes for the preparation of steroids in general
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J21/00—Normal steroids containing carbon, hydrogen, halogen or oxygen having an oxygen-containing hetero ring spiro-condensed with the cyclopenta(a)hydrophenanthrene skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J73/00—Steroids in which the cyclopenta[a]hydrophenanthrene skeleton has been modified by substitution of one or two carbon atoms by hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2103/00—Systems containing at least three condensed rings
- C07C2103/02—Ortho- or ortho- and peri-condensed systems
- C07C2103/04—Ortho- or ortho- and peri-condensed systems containing three rings
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Frank et al. | Synthesis of novel steroidal 17α-triazolyl derivatives via Cu (I)-catalyzed azide-alkyne cycloaddition, and an evaluation of their cytotoxic activity in vitro | |
Wölfling et al. | Neighboring group participation: Part 15. Stereoselective synthesis of some steroidal tetrahydrooxazin-2-ones, as novel presumed inhibitors of human 5α-reductase | |
Wölfling et al. | Synthesis and receptor-binding examinations of the normal and 13-epi-D-homoestrones and their 3-methyl ethers | |
Magyar et al. | Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and D-homosteroids by intramolecular cyclization reactions | |
Kiss et al. | Stereocontrolled synthesis of the four possible 3-methoxy and 3-benzyloxy-16-triazolyl-methyl-estra-17-ol hybrids and their antiproliferative activities | |
Parish et al. | Sterol synthesis. A simplified method for the synthesis of 32-oxygenated derivatives of 24, 25-dihydrolanosterol. | |
Kiss et al. | Stereoselective synthesis of the four 16-hydroxymethyl-3-methoxy-and 16-hydroxymethyl-3-benzyloxy-13α-estra-1, 3, 5 (10)-trien-17-ol isomers and their antiproliferative activities | |
Purushottamachar et al. | A new simple and high-yield synthesis of 5α-dihydrotestosterone (DHT), a potent androgen receptor agonist | |
Nahar et al. | Synthesis of ester-linked lithocholic acid dimers | |
Tapolcsányi et al. | Synthesis and receptor-binding examination of 16-hydroxymethyl-3, 17-estradiol stereoisomers | |
Bjedov et al. | Synthesis and antitumor activity of alkylated bile acids and oxazolines | |
Watanabe et al. | Benzothieno and benzofurano annelated estranes | |
Kiss et al. | Novel preparation of substituted oxazolines condensed to d-ring of estrane skeleton and characterization of their antiproliferative properties | |
Zhou et al. | A new highly stereoselective construction of the sidechain of squalamine through improved Sharpless catalytic asymmetric dihydroxylation | |
Marcos-Escribano et al. | 1, 2-Dehydrogenation of steroidal 6-methylen derivatives. Synthesis of exemestane | |
Faraj et al. | Synthesis of new steroidal 11β-substituted spirolactones | |
Oumzil et al. | First total synthesis of (±)-3-aza-11-oxa-1, 3, 5 (10)-trieno steroids | |
Di Chenna et al. | PhI NSes mediated aziridination of 11-pregnane derivatives: synthesis of an 11, 12-aziridino analogue of neuroactive steroids | |
Marek et al. | A facile method for steroid labeling by heavy isotopes of hydrogen | |
Qin et al. | A highly efficient synthesis of 22-deoxy-OSW-1 by utilizing the intact skeleton of diosgenin | |
Wang et al. | The regio-and stereo-selective reduction of steroidal 4-en-3-ones using Na2S2O4/NaHCO3 and CuCl/NaBH4 | |
CN101508717B (en) | Synthesis of tuberculosis resistant compound of arguesterol | |
CN105693801B (en) | The aryl androstane 5 (6), 8 (14) of 3 β hydroxyls 16, the synthetic method of the ketone of 15 (16) triolefin 17 | |
Wang et al. | Novel and efficient synthesis of 22-alkynyl-13, 24 (23)-cyclo-18, 21-dinorchol-22-en-20 (23)-one analogues | |
Salunke et al. | An efficient method for the synthesis of methyl 11α-amino-3α, 7α-diacetoxy-12-oxo-5β-cholan-24-oate |