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yuncheng6: ½ð±Ò+5 2015-03-29 21:16:16
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yuncheng6: ½ð±Ò+5 2015-03-29 21:16:16
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1 . compound 9A ÏàËÆ¶È:72% Steroids 1989 54 1-10 Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones Richard W. Draper, Mohindar S. Puar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 9D ÏàËÆ¶È:64% Steroids 1989 54 1-10 Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones Richard W. Draper, Mohindar S. Puar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 17¦Á,21-Dihydroxy-9¦Â,11¦Â-epoxy-16¦Á-methylpregna-1,4-diene-3,20-dione 21-acetate C24H30O6 ÏàËÆ¶È:64% Steroids 2013 78 1281-1287 Expedient synthesis of 17¦Á,21-dihydroxy-9¦Â,11¦Â-epoxy-16¦Á-methylpregna-1,4-diene-3,20-dione 21-acetate from prednisolone utilising a novel Mattox rearrangement David G. Hulcoop, Peter D.P. Shapland Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 3-acetoxycladiell-11(17)-en-6-one C22H34O4 ÏàËÆ¶È:60% Journal of Natural Products 1994 Vol 57 574 New Cladiellane Diterpenes from the Soft Coral Cladiella australis of the Andaman and Nicobar Islands C. Bheemasankara Rao, D. Sreenivasa Rao, C. Satyanarayana, D. Venkata Rao, Katharina E. Kass¨¹hlke, D. John Faulkner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . ( 11 ¦Â,16¦Á)-21-A cetylo xy-9-fluoro-11,16,17-trihydroxypregna-1,4-diene-3,20-dione ÏàËÆ¶È:60% Steroids 1994 59 196-204 A reinvestigation of the D-homoannular rearrangement and subsequent degradation pathways of(11¦Â,16¦Á)-9-Fluoro-11,15,17,21-tetrahydroxypregna-1,4-diene-3,20-dione(triamcinolone) Edward J. Delaney, Ronald G. Sherrill, Venkatapuram Palaniswamy, Thomas C. Sedergran, Stephan P. Taylor Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 9¦Á-fluoro-11¦Â,16¦Á,17¦Á-trihydroxy-17¦Â-hydroxymethyl-D-homoandrosta-1,4-diene-3,17a-dione ÏàËÆ¶È:60% Steroids 1989 53 513-531 Recognition of d-homoannulation by proton and carbon NMR spectra Leland L. Smith, Edward L. Ezell Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 17¦Â-(N-octylamino)-4-methyl-4-aza-5¦Á-androstan-3-one C27H48N2O ÏàËÆ¶È:60% Journal of Medicinal Chemistry 1995 38 1158-1173 Synthesis and in Vitro Activity of 17.beta.-(N-Alkyl/arylformamido and N-alkyl/arylalkyl/arylamido)-4-methyl-4-aza-3-oxo-5.alpha.-androstan-3-ones as Inhibitors of Human 5.alpha.-Reductases and Antagonists of the Androgen Receptor Xun Li, Shankar M. Singh, Fernand Labrie Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 21-acetoxy-9¦Á-bromo-11¦Â-formyl-17¦Á-hydroxy-16¦Á-methyl-1,4-dien-3-one(6,7,9,10,13,14) ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 1994 32 547-549 13C NMR spectroscopy of some 20-ketopregnanes Jos¨¦ Alberto Ruiz Garcia, Fernando A. Verdecia Navarro and Herm¨¢N T. V¨¦lez Castro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 17¦Â-(N-heptylamino)-4-methyl-4-aza-5¦Á-androstan-3-one C26H46N2O ÏàËÆ¶È:57.6% Journal of Medicinal Chemistry 1995 38 1158-1173 Synthesis and in Vitro Activity of 17.beta.-(N-Alkyl/arylformamido and N-alkyl/arylalkyl/arylamido)-4-methyl-4-aza-3-oxo-5.alpha.-androstan-3-ones as Inhibitors of Human 5.alpha.-Reductases and Antagonists of the Androgen Receptor Xun Li, Shankar M. Singh, Fernand Labrie Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Notoamide B C26H29N3O4 ÏàËÆ¶È:57.6% Angewandte Chemie International Edition 2008 47 3573-3577 Isolation, Structure Elucidation, and Biomimetic Total Synthesis of Versicolamide B, and the Isolation of Antipodal ( )-Stephacidin A and (+)-Notoamide B from Aspergillus versicolor NRRL 35600** Thomas J. Greshock, Alan W. Grubbs, Ping Jiao, Donald T. Wicklow, James B. Gloer, and Robert M. Williams* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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