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xifangchenqu

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[ÇóÖú] ΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë

13C-NMR:14.08,21.71,22.62,22.67,23.10,24.65,25.30,31.68,32.39,35.61,36.08,37.44,38.77,50.74,56.23,62.72,71.27,71.95,72.77,76.07,125.11,128.43,170.94,174.48
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xifangchenqu: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-02-04 23:10:27
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1 .     3¦Â-Acetoxy-5¦Á,6¦Á-epoxypregnan-20-one
    ÏàËÆ¶È:66.6%
Molecules          2009          14          4655-4668
Synthesis of Pregnane Derivatives, Their Cytotoxicity on LNCap and PC-3 Cells, and Screening on 5¦Á-Reductase Inhibitory Activity
Sujeong Kim and Eunsook Ma
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     3¦Â-acetoxy-5¦Â,6¦Â-epoxypregnan-20-one
    ÏàËÆ¶È:66.6%
Molecules          2009          14          4655-4668
Synthesis of Pregnane Derivatives, Their Cytotoxicity on LNCap and PC-3 Cells, and Screening on 5¦Á-Reductase Inhibitory Activity
Sujeong Kim and Eunsook Ma
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     methyl 3¦Â-acetoxy-5¦Â-androstane-17¦Â-carboxylate
    ÏàËÆ¶È:66.6%
Magnetic Resonance in Chemistry          1986          24          185-189
Studies on the conformations in solution of 5¦Â-steroids having different side chains by 13C NMR spectroscopy
A. M. Seldes, M. E. Deluca and E. G. Gros
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     3¦Â-acetoxy-5¦Â,6¦Â-epoxy-20-hydroxyiminopregnan-20-one
    ÏàËÆ¶È:62.5%
Molecules          2009          14          4655-4668
Synthesis of Pregnane Derivatives, Their Cytotoxicity on LNCap and PC-3 Cells, and Screening on 5¦Á-Reductase Inhibitory Activity
Sujeong Kim and Eunsook Ma
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     2-(Trimethylsilyl)ethyl3¦Â-nitratoandrost-5-ene-17¦Â-carboxylate
C25H41NO5Si     ÏàËÆ¶È:62.5%
Steroids          2005          70          615-625
Etienic etienate as synthon for the synthesis of steroid oligoester gelators
Pavel Drašar, Miloš Bud¨§š¨ªnsky, Miroslav Reschel, Vladim¨ªr Pouzar, Ivan Černy
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     3¦Â,4¦Â-dihydroxy-pregn-5-en-20-one-3-sulfate 4-acetate
    ÏàËÆ¶È:62.5%
Journal of Natural Products          1989          Vol 52          657
A New Sterol Sulfate from the Marine Sponge Stylopus australis
Michele R. Prinsep, John W. Blunt, Murray H. G. Munro
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     15-acetoxy-7-labden-17-oic acid
    ÏàËÆ¶È:62.5%
Phytochemistry          1987          26          3037-3040
Labdane diterpenoids from Halimium viscosum and H. verticilatum
Julio G. Urones,Isidro S¨¢nchez Marcos,David Diez Martin,F.M.S.Brito Palma,Jes¨²s M. Rodilla
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     compound 9
    ÏàËÆ¶È:62.5%
Phytochemistry          1990          29          2927-2930
Diterpenoids of Halimium viscosum
Julio G. Urones,Isidro Sanchez Marcos,Narciso Martin Garrido,Pilar Basabe Barcala
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     octanoyl fellutamide
    ÏàËÆ¶È:62.5%
Bioorganic & Medicinal Chemistry Letters          2006          16          3855-3858
Neurotrophic peptide aldehydes: Solid phase synthesis of fellutamide B and a simplified analog
John S. Schneekloth Jr., John L. Sanders, John Hines, Craig M. Crews
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     3¦Á-acetoxy-11¦Á-hydroxyy-5¦Â-pregnan-20-one
C23H36O4     ÏàËÆ¶È:62.5%
Bioorganic & Medicinal Chemistry          2008          16          3831-3838
Synthesis and GABAA receptor activity of oxygen-bridged neurosteroid analogs
Lautaro D. Alvarez, Adriana S. Veleiro, Ricardo F. Baggio, Mar¨ªa T. Garland, Valeria C. Edelsztein, H¨¦ctor Coirini, Gerardo Burton
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     3¦Â-acetoxy-5¦Â-pregnan-20-one
    ÏàËÆ¶È:62.5%
Magnetic Resonance in Chemistry          1986          24          185-189
Studies on the conformations in solution of 5¦Â-steroids having different side chains by 13C NMR spectroscopy
A. M. Seldes, M. E. Deluca and E. G. Gros
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     3¦Â,20R-bis(acetoxy)-5¦Â-12¦Á-hydroxy-pregn-14-ene
C25H38O5     ÏàËÆ¶È:62.5%
Steroids          2011          76          1166-1175
Norrish¨CPrins reaction as a key step in the synthesis of 14¦Â-hydroxy-5¦Á (or 5¦Â or ¦¤5,6)-pregnane derivatives
Philippe Geoffroy, Blandine Ressault, Eric Marchioni, Michel Miesch
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     17¦Â-(2',5'-Dihydro-5'-oxo-3'-furyl)androst-4-en-3-one
C23H30O3     ÏàËÆ¶È:62.5%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     17¦Â-(2',5'-Dihydro-5'-oxo-3'-furyl)androst-4-en-3-one
C23H30O3     ÏàËÆ¶È:62.5%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     20-Oxo-5¦Â-pregnan-3¦Á-yl N-(tert-butoxycarbonyl)-L-glutamyl 1-ester
    ÏàËÆ¶È:60.7%
Steroids          2012          77          282-287
Synthesis of deuterium labeled NMDA receptor inhibitor ¨C 20-Oxo-5¦Â-[9,12,12-2H3]pregnan-3¦Á-yl-l-glutamyl 1-ester
Vojtech Kapras, Alena Slavickova, Eva Stastna, Ladislav Vyklicky Jr., Karel Vales, Hana Chodounska
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     thevetiogenin 3-acetate
C25H34O5     ÏàËÆ¶È:60%
Phytochemistry          1992          31          251-254
C-nor-d-Homo-cardenolide glycosides from Thevetia neriifolia
Fumiko Abe, Tatsuo Yamauchi, Toshihiro Nohara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     compound 6a
C25H40O5     ÏàËÆ¶È:60%
European Journal of Organic Chemistry          2011                   5383-5389
Intrapopulation Variability in the Terpene Metabolism of the Antarctic Opisthobranch Mollusc Austrodoris kerguelenensis
Adele Cutignano, Wen Zhang, Conxita Avila, Guido Cimino and Angelo Fontana
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     chlorohydrin
    ÏàËÆ¶È:59.2%
Chemical & Pharmaceutical Bulletin          1995          43          2253-2255
Clerodane Diterpenoids from Ajuga decumbens
Huan-ming CHEN,Zhi-da MIN,Munekazu IINUMA and Toshiyuki TANAKA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     cholest-5-ene-2¦Â,3¦Á,21-triol
    ÏàËÆ¶È:59.2%
Chemistry of Natural Compounds          1990          26          408-411
STEROID COMPOUNDS FROM OPHIUROIDS II. SULFATED STEROIDS FROM Ophiura sarsi AND Ophiura leptoctenia
E. V. Levina, S. N. Fedorov, V. A. Stonik,P. V. Andriyashchenko, A. I. Kalinovskii,and V. V. Isakov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     9¦Á,11¦Á-Epoxy-5¦Á-cholest-7-enr-3¦Â,5,6¦Â-triol
C27H44O4     ÏàËÆ¶È:59.2%
Steroids          1991          56          154-158
Synthesis of the marine epoxy sterol 9¦Á,11¦Á-epoxy-5¦Á-cholest-7-ene-3¦Â,5,6¦Â-triol
Anna Migliuolo, Giacomo Notaro, Vincenzo Piccialli, Donato Sica
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     4¦Â-hydroxycholesterol(3¦Â,4¦Â-dihydroxy-5-cholestene)
C27H46O2     ÏàËÆ¶È:59.2%
Tetrahedron          2012          68          6485-6491
Oxidation with selenium dioxide: the first report of solvent-selective steroidal aromatization, efficient access to 4¦Â,7¦Á-dihydroxy steroids, and syntheses of natural diaromatic ergosterols
Pranab Ghosh, Jayanta Das, Antara Sarkar, Seik Weng Ng, Edward R.T. Tiekink
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-01-21 08:49:36
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3Â¥2015-02-26 09:47:46
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