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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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3Â¥2015-06-05 07:27:43
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ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
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250350663: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-05 07:27:47
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250350663: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-05 07:27:47
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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

2Â¥2015-06-04 19:41:48














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