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¦Ä C (151 MHz, CDCl3) 11.63, 11.81, 11.97, 12.02, 12.25, 18.24, 18.79, 18.83, 18.98, 19.01, 19.15, 19.81, 20.68, 21.07, 21.21, 21.29, 23.05, 24.29, 24.36, 25.38, 25.88, 26.07, 26.38, 26.45, 28.28, 28.55, 28.93, 29.12, 29.16, 29.69, 31.36, 31.56, 31.87, 33.00, 33.90, 33.96, 35.83, 36.10, 36.93, 37.50,36.99, 37.39, 39.07, 39.16, 39.44, 39.54, 40.35, 40.45, 40.91, 41.72, 41.99, 42.25, 42.81, 42.92, 45.83, 48.24, 49.41, 49.49, 51.23, 55.27, 55.35, 55.69, 55.74, 55.94, 56.02, 65.36, 71.36, 71.45, 73.35 , 123.86 , 125.41, 125.43, 129.33, 129.47, 138.12, 138.22, 143.44, 143.47, 146.24, 209.27
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1 .     (cis)-(3¦Á,5¦Â,7¦Á,12¦Á)-24-{[2-(4-{2-[(ethoxycar-bonyl)amino]ethoxy}benzyl)cyclohexyl]oxy}-7,12-bis(formyloxy)-24-oxocholan-3-yl-(3¦Â,22E)-stigmasta-5,22-dien-3-yl butanedioate
    ÏàËÆ¶È:65%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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2 .     (cis)-(3¦Á,5¦Â,7¦Á,12¦Á)-7,12-bis(formyloxy)-24-oxo-24-[(3¦Â,22E)-stigmasta-5,22-dien-3-yloxy]cholan-3-yl-2-{4-{2-[(ethoxycarbonyl)amino]ethoxy}benzyl}cyclohexylbutanedioate
    ÏàËÆ¶È:65%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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3 .     (trans)-(3¦Á,5¦Â,7¦Á,12¦Á)-7,12-bis(formyloxy)-24-oxo-24-[(3¦Â,22E)-stigmasta-5,22-dien-3-yloxy]cholan-3-yl-2-{4-{2-[(ethoxycarbonyl)amino]ethoxy}benzyl}cyclohexylbutanedioate
    ÏàËÆ¶È:65%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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4 .     (trans)-(3¦Á,5¦Â,7¦Á,12¦Á)-24-{[2-(4-{2-[(ethoxycar-bonyl)amino]ethoxy}benzyl)cyclohexyl]oxy}-7,12-bis(formyloxy)-24-oxocholan-3-yl-(3¦Â,22E)-stigmasta-5,22-dien-3-yl butanedioate
    ÏàËÆ¶È:63.7%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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5 .     3¦Â-hexadecanoyloxy-lup-20(29)-en-21-ol
C46H80O3     ÏàËÆ¶È:61.2%
Chemistry of Natural Compounds          2011          Vol. 47, No. 3          404-407
A NEW ACYLATED TRITERPENE WITH ANTIMICROBIAL ACTIVITY FROM THE LEAVES OF Rauvolfia vomitoria
Simone Veronique Fannang, Victor Kuete, Celine Djama Mbazoa, Joseph Itbert Momo, Hanh Trinh Van-Dufat, Francois Tillequin, Elisabeth Seguin, Elizabeth Chosson, and Jean Wandji1*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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6 .     cyclo[O-[[[N-[(2S,3S,4S)-4-[(1S,2S)-3-amino-2-methoxy-cyclohexanecarbonyl]oxy]-3-oxo-2,5-dimethylhexanoyl]-L-leucyl]-L-prolyl]-N,O-dimethyl-L-tyrosyl]-L-threonyl] hydrochloride
C42H64N5O11Cl     ÏàËÆ¶È:55%
The Journal of Organic Chemistry          1996          61          1655-1664
Synthetic Routes to a Constrained Ring Analog of Didemnin B
Scott C. Mayer, Amy J. Pfizenmayer, and Madeleine M. Joulli¨¦
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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7 .     compound 20
C43H68N6O7S     ÏàËÆ¶È:53.7%
Journal of the American Chemical Society          2011          132          7692-7695
The Multiple Multicomponent Approach to Natural Product Mimics: Tubugis, N-Substituted Anticancer Peptides with Picomolar Activity
Orlando Pando, Sebastian Stark, Annika Denkert, Andrea Porzel, Rainer Preusentanz, and Ludger A. Wessjohann
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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8 .     N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methylleucyl-norvalylsarcosyl-N-methylleucylvalyl-N-methylleucyl-alanine benzyl ester
C59H85N7O10     ÏàËÆ¶È:53.0%
The Journal of Organic Chemistry          2000          65          2951-2958
Total Synthesis of Cyclosporin O Both in Solution and in the Solid Phase Using Novel Thiazolium-, Immonium-, and Pyridinium-Type Coupling Reagents:  BEMT, BDMP, and BEP1
Peng Li and Jie Cheng Xu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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