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250350663

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13C NMR (100 MHz, DMSO) ¦Ä33.8, 34.3, 34.4, 34.6, 38.5, 40.3, 40.7, 46.2, 50.0, 55.0, 55.9, 59.1, 64.2, 64.4, 69.8, 72.1, 84.5, 99.6, 141.9, 155.6,195.7
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250350663

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2Â¥: Originally posted by seuseasoar at 2015-06-04 19:41:48
1 .     drevogenin D
    ÏàËÆ¶È:57.1%
Phytochemistry          2002          61          383-388
Polyoxypregnane glycosides from the flowers of Dregea volubilis
Niranjan P. Sahu, Nilendu Panda,  ...

3Â¥2015-06-05 07:27:43
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seuseasoar

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250350663: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-05 07:27:47
1 .     drevogenin D
    ÏàËÆ¶È:57.1%
Phytochemistry          2002          61          383-388
Polyoxypregnane glycosides from the flowers of Dregea volubilis
Niranjan P. Sahu, Nilendu Panda, Nirup B. Mandal,SukdebBanerjee, Kazuo Koike, Tamotsu Nikaido
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     drevogenin P
    ÏàËÆ¶È:57.1%
Phytochemistry          2002          61          383-388
Polyoxypregnane glycosides from the flowers of Dregea volubilis
Niranjan P. Sahu, Nilendu Panda, Nirup B. Mandal,SukdebBanerjee, Kazuo Koike, Tamotsu Nikaido
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     compound 25a
    ÏàËÆ¶È:52.3%
Biochemical Systematics and Ecology          2009          37          133-137
Chemical constituents of Pteris cretica Linn. (Pteridaceae)
Liva Harinantenaina, Katsuyoshi Matsunami, Hideaki Otsuka
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     ent-11¦Á,13,15¦Â-trihydroxy-kaur-16-ene triacetate
C24H34O4     ÏàËÆ¶È:52.3%
Phytochemistry          1992          31          3845-3849
Biotransformation of two ent-15¦Â-hydroxy-kaur-16-ene derivatives by Gibberella fujikuroi
Braulio M. Fraga, Melchor G. Hern¨¢ndez, Pedro Gonz¨¢lez
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     drevogenin D
    ÏàËÆ¶È:52.3%
Phytochemistry          1988          27          1451-1458
Structural revision of pregnane ester glycosides from condurango cortex and new compounds
S. Berger,P. Junior,L. Kopanski
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     Aulacocarpin C
C20H34O4     ÏàËÆ¶È:52.3%
Tetrahedron          2007          63          8993-8998
Trypanocidal labdane diterpenoids from the seeds of Aframomum aulacocarpos (Zingiberaceae)
Sylvain Val¨¨re T. Sob, Pierre Tane, Bonaventure T. Ngadjui, Joseph D. Connolly, Dawei Ma
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     Drevogenin D
C21H34O5     ÏàËÆ¶È:52.3%
Tetrahedron          2003          59          8399-8403
Polyhydroxy pregnanes from Dregea volubilis
Nilendu Panda, Nirup B Mondal, Sukdeb Banerjee, Niranjan P Sahu, Kazuo Koike, Tamotsu Nikaido, Manuela Weber, Peter Luger
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     11¦Á-hydroxyprogesterone
    ÏàËÆ¶È:52.3%
Steroids          2013          78          1152-1158
Biocatalyst mediated production of 6¦Â,11¦Á-dihydroxy derivatives of 4-ene-3-one steroids
Swati P. Kolet, Siddiqui Niloferjahan, Saikat Haldar, Rajesh Gonnade, Hirekodathakallu V. Thulasiram
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     euryspongiol A5
C26H44O7     ÏàËÆ¶È:52.1%
Tetrahedron          1994          50          3813-3828
Euryspongiols: Ten new highly hydroxylated 9,11-secosteroids with antihistaminic activity from the sponge euryspongia sp. Stereochemistry and reduction.
Jos¨¦ Dopeso, Emilio Quiño¨¢, Ricardo Riguera, C¨¦cile Debitus, Patricia R. Bergquist
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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2Â¥2015-06-04 19:41:48
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