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namujila½ð³æ (ÕýʽдÊÖ)
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nmjl12 ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (101 MHz, Acetone) ¦Ä 7.01, 13.92, 23.39, 24.59, 25.89, 25.99, 30.69, 30.78, 31.40, 36.65, 39.65, 51.32, 77.43, 102.78, 156.44, 170.96, 173.96, 198.75 |
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yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
2Â¥2015-03-22 15:06:17
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
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namujila: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-22 15:22:46
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namujila: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-22 15:22:46
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1 . Methyl (3R*,6S*,Z)-4,6-diethyl-3,6-epidioxydodeca-4-enoate C17H30O4 ÏàËÆ¶È:61.1% Journal of Natural Products 2005 68 759-761 Cyclic Peroxides Derived from the Marine Sponge Plakortis simplex Michael Holzwarth, Jean-Michel Trendel, Pierre Albrecht, Armin Maier, and Walter Michaelis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (2S,3R,4R)-4-acetamido-2-tetradecyltetrahydrofuran-3-yl acetate C22H41NO4 ÏàËÆ¶È:61.1% Tetrahedron 2013 69 8228-8244 A common approach to the total synthesis of l-arabino-, l-ribo-C18-phytosphingosines, ent-2-epi-jaspine B and 3-epi-jaspine B from d-mannose Miroslava Martinkov¨¢, Kvetoslava Pomikalov¨¢, Jozef Gonda, M¨¢ria Vilkov¨¢ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (2S,3R,4R)-1-O-[2-deoxy-2-iodo-¦Â-D-galactopyranosyl]-2-hexacosanoylamino-1,3,4-octadecantriol C50H98INO8 ÏàËÆ¶È:57.1% Molecules 2014 19 10090-10102 Synthesis of a 2''-Deoxy-¦Â-GalCer Meena S. Thakur, Archana Khurana, Mitchell Kronenberg and Amy R. Howell Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . methyl 11-hydroxyhexadecanoate ÏàËÆ¶È:55.5% Chemical & Pharmaceutical Bulletin 1997 45 1955-1960 Resin Glycosides. XXV. Multifidins I and II, New Jalapins, from the Seed of Quamoclit x multifida Masateru ONO,Fumiko HONDA(nee YAMADA),Ariaki KARAHASHI,Toshio KAWASAKI and Kazumoto MIYAHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . methyl 11-hydroxyhexadecanoate ÏàËÆ¶È:55.5% Chemical & Pharmaceutical Bulletin 1997 45 1955-1960 Resin Glycosides. XXV. Multifidins I and II, New Jalapins, from the Seed of Quamoclit x multifida Masateru ONO,Fumiko HONDA(nee YAMADA),Ariaki KARAHASHI,Toshio KAWASAKI and Kazumoto MIYAHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . methyl 11S-jalapinolate ÏàËÆ¶È:55.5% Chemical & Pharmaceutical Bulletin 2011 59(9) 1163-1168 Identification and Characterization of Component Organic and Glycosidic Acids of Crude Resin Glycoside Fraction from Calystegia soldanella Ayako TAKIGAWA, Hiroaki SETOGUCHI, Masafumi OKAWA, Junei KINJO, Hiroyuki MIYASHITA, Kazumi YOKOMIZO, Hitoshi YOSHIMITSU, Toshihiro NOHARA, and Masateru ONO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Dodecyl-N-6-acryloylaminohexylamino-3,5-dideoxy-2-thio-D-glycero-D-galacto-2-nonulopyranosaminic acid ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2012 20 446-454 Synthesis and biological evaluation of sialic acid derivatives containing a long hydrophobic chain at the anomeric position and their C-5 linked polymers as potent influenza virus inhibitors Kaori Suzuki, Tetsuo Koyama, Sangchai Yingsakmongkon, Yasuo Suzuki, Ken Hatano,Koji Matsuoka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . solid A ÏàËÆ¶È:55.5% Chinese Traditional and Herbal Drugs 2010 41 851-854 Three ceramides from gorgonian Echinogorgia sp. LIAO Liu; WANG Nan; LIANG Qiu; LIAO Xiao-jian; XU Shi-hai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (1'S,2R,4R)-2-tert-Butyl-4-(1-hydroxypentyl)-oxazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 4-methyl ester ÏàËÆ¶È:55.5% Tetrahedron Letters 2004 45 3063-3065 Highly diastereoselective aldol additions to five-ring N,O-acetals Martin Brunner, Ari M.P Koskinen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (+)-Pinanediol hexaneboronate C16H29BO2 ÏàËÆ¶È:55.5% Organic & Biomolecular Chemistry 2004 2 38-47 Total synthesis of (− -microcarpalide, a novel microfilament disrupting metabolitePaolo Davoli, Alberto Spaggiari, Luca Castagnetti and Fabio Prati Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Dimethyl [2-Oxo-3-(6-pentyltetrahydro-2H-pyran-2-yl)propy]phosphonate C15H29O5P ÏàËÆ¶È:55.5% European Journal of Organic Chemistry 2012 801-809 (E)-Dimethyl 2-Oxopent-3-enylphosphonate: An Excellent Substrate for Cross-Metathesis ¨C Easy Access to Functionalized Heterocycles Thomas Cochet, Didier Roche, V¨¦ronique Bellosta and Janine Cossy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (5R,6S,9S)-(-)-3-(6-butyl-3-oxohexahydrooxazolo[3,4-a]pyridin-5-yl)propionic acid methyl ester C15H25NO4 ÏàËÆ¶È:55.5% Tetrahedron 2005 61 1187-1198 Enantioselective syntheses of two 5, 9E diastereomers of 223V, an alkaloid from the poison frog Dendrobates pumilio Naoki Toyooka, Hideo Nemoto, Masashi Kawasaki, H. Martin Garraffo, Thomas F. Spande, John W. Daly Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2015-03-22 15:07:53









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-microcarpalide, a novel microfilament disrupting metabolite