| ²é¿´: 374 | »Ø¸´: 1 | |||
·çÐÅ×Ó0208ľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð»£¡ ÒÑÓÐ1È˲ÎÓë
|
| 13C NMR (151 MHz, CDCl3) ¦Ä 14.07, 14.12, 22.58, 22.70, 24.69, 25.63, 27.16, 27.19, 27.21, 27.22, 29.04, 29.07, 29.15, 29.25, 29.33, 29.35, 29.37, 29.44, 29.53, 29.60, 29.65, 29.66, 29.68, 29.69, 29.70, 29.77, 31.53, 31.91, 31.93, 34.07, 65.03, 127.90, 128.07, 129.73, 130.02, 130.22, 180.02. |
» ²ÂÄãϲ»¶
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ36È˻ظ´
275Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
µ÷¼ÁÇóÊÕÁô
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
070300»¯Ñ§Ñ§Ë¶311·ÖÇóµ÷¼Á
ÒѾÓÐ19È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ13È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ33È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó 085600 277 12²Ä¿Æ»ùÇóµ÷¼Á
ÒѾÓÐ17È˻ظ´
»¹Óл¯¹¤¶þÂÖµ÷¼ÁµÄѧУÂð
ÒѾÓÐ47È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬¿É·ñÓÐÈËÖ¸µã»òÔõÑù²éµ½´øÓÐÒÑÖªµ¥ÌåµÄºË´ÅÆ×Êý¾ÝÎÄÏ×
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
ÇóÖú»¯ºÏÎï΢Æ×ËÑË÷
ÒѾÓÐ8È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
¼±¼±¼±¡£¡£¡£¡£ÇóÖú΢Æ×Êý¾Ý£¨50%ÏàËÆ¶È¾ÍOKÁË£©£¬²»Ê¤¸Ðл£¡
ÒѾÓÐ8È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÈË΢Æ×²éѯ£¬¼±£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48426.9
- ºì»¨: 52
- Ìû×Ó: 6748
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
·çÐÅ×Ó0208: ½ð±Ò+10, ¡ïÓаïÖú 2015-04-22 21:59:00
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
·çÐÅ×Ó0208: ½ð±Ò+10, ¡ïÓаïÖú 2015-04-22 21:59:00
|
1 . Triolein ÏàËÆ¶È:78.3% Magnetic Resonance in Chemistry 2000 38 886-890 Concentration dependence of 13C NMR spectra of triglycerides: implications for the NMR analysis of olive oils Luisa Mannina, Claudio Luchinat, Maurizio Patumi, Maria Carmela Emanuele, Enrico Rossi and Annalaura Segre Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Tri-11-eicosenoin ÏàËÆ¶È:78.3% Magnetic Resonance in Chemistry 2000 38 886-890 Concentration dependence of 13C NMR spectra of triglycerides: implications for the NMR analysis of olive oils Luisa Mannina, Claudio Luchinat, Maurizio Patumi, Maria Carmela Emanuele, Enrico Rossi and Annalaura Segre Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . AL072 C41H76O5 ÏàËÆ¶È:78.0% The Journal of Antibiotics 1995 48 773-779 AL072, A Novel Anti-Legionella Antibiotic Produced by Streptomyces sp. CHANGSUEK YON, JUNG-WOO SUH, JUN-HWAN CHANG, YOONGHO LIM, CHUL-HOON LEE, YEONG-SEON LEE, YONG-WOO LEE Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-[(10Z,13Z)-Octadeca-10,13-dien-1-yloxy]propane-1,2-diol C21H40O3 ÏàËÆ¶È:71.0% Chemistry & Biodiversity 2011 8 287-299 Synthesis of Lipid¨COligonucleotide Conjugates for RNA Interference Studies Santiago Grijalvo, Sandra M. Ocampo, Jos¨¦ C. Perales and Ramon Eritja Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . petrocortyne C C46H70O3 ÏàËÆ¶È:70.7% Tetrahedron 1998 54 447-462 Petrocortynes and petrosiacetylenes, novel polyacetylenes from a sponge of the genus Petrosia Youngwan Seo, Ki Woong Cho, Jung-Rae Rho, Jongheon Shin, Chung J. Sim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Trilinolein ÏàËÆ¶È:67.5% Magnetic Resonance in Chemistry 2000 38 886-890 Concentration dependence of 13C NMR spectra of triglycerides: implications for the NMR analysis of olive oils Luisa Mannina, Claudio Luchinat, Maurizio Patumi, Maria Carmela Emanuele, Enrico Rossi and Annalaura Segre Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (6S,7S,9R,10R)-6,9-epoxynonadec-18-ene-7,10-diol 10-hexadecanonate C19H34O2 ÏàËÆ¶È:67.5% Australian Journal of Chemistry 1990 43 895-911 Epoxy Lipids From the Australian Epiphytic Brown Alga Notheia anomala RA Barrow and RJ Capon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . (2S,3R,4E)-2-[(3''-stearoyloxy)triacontanamido]octadec-4-ene-1,3-diol C66H129NO5 ÏàËÆ¶È:67.5% Bioscience, Biotechnology, and Biochemistry 2012 76 1715-1720 Synthesis of Sphingolipids with an ¦Ø-Esterified Long Acyl Chain, Ceramide Components of the Human Epidermis Takuya TASHIRO, Kenji MORI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . mayolene-16 C34H60O4 ÏàËÆ¶È:67.5% The Journal of Organic Chemistry 2002 67 5896-5900 Synthesis of Mayolene-16 and Mayolene-18: Larval Defensive Lipids from the European Cabbage Butterfly Douglas B. Weibel, Laura E. Shevy, Frank C. Schroeder, and Jerrold Meinwald Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . isofulvinol C46H76O2 ÏàËÆ¶È:67.5% Journal of Natural Products 2014 77 1678-1684 Sequestered Fulvinol-Related Polyacetylenes in Peltodoris atromaculata M. Letizia Ciavatta, Genoveffa Nuzzo, Kentaro Takada, V¨¦ronique Mathieu, Robert Kiss, Guido Villani, and Margherita Gavagnin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . (2S,3R,4E,6R)-2-[(3''-stearoyloxy)triacontanamido]octadec-4-ene-1,3,6-triol C66H129NO6 ÏàËÆ¶È:66.6% Bioscience, Biotechnology, and Biochemistry 2012 76 1715-1720 Synthesis of Sphingolipids with an ¦Ø-Esterified Long Acyl Chain, Ceramide Components of the Human Epidermis Takuya TASHIRO, Kenji MORI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-04-22 19:01:36













»Ø¸´´ËÂ¥
10