| ²é¿´: 204 | »Ø¸´: 1 | ||
¶¹Þ¢-Ä껪ľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý¿â£¡
|
| 21.29, 22.59, 22.83, 22.93, 26.22, 27.06, 31.77, 34.16, 40.78, 46.04, 47.32, 48.42,52.09, 55.85, 61.76, 61.95, 74.26, 74.85, 80.86, 83.64, 107.55, 112.41, 121.13, 120.01. |
» ²ÂÄãϲ»¶
301Çóµ÷¼Á
ÒѾÓÐ18È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
328Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ28È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ21È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ33È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ41È˻ظ´
331Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
298Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
×öÒ»¸ö½çÃæ»¯µÄÊý¾Ý¿â£¬ÓÃʲôÓïÑԺã¿
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ Èý¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
MestReNovaÎÞ·¨½øÐл¯ºÏÎï½á¹¹ÇâÆ×Ô¤²â
ÒѾÓÐ12È˻ظ´
ÇóÖúÈý¸ö»¯ºÏÎ̼Æ×£©µÄ΢Æ×Êý¾Ý¿â¼ìË÷½á¹û£¨ÏàËÆ¶Èǰ20%£©
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ3¸ö»¯ºÏÎïµÄÄ£ºý²éÕÒ£¨¡·80%£©
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï~¼±~£¡Ð»Ð»
ÒѾÓÐ3È˻ظ´
asp.netÖдÓÊý¾Ý¿â¶Á³öͼƬ²¢ÇÒÏÔʾ³öÀ´ ·¾¶
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²é»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
¼±Çó΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÇëÎÊÓÐûÓÐÒ»¸ö»¯ºÏÎï±ê×¼Æ×ͼ½âÎöÊý¾Ý¿â£¿
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿Ì¼Æ×ÖÐȱÉÙÒÔôÊ»ù̼Êý¾Ý
ÒѾÓÐ12È˻ظ´
¡¾ÇóÖú¡¿ÎÒ¹úÓÐÄÄЩÖÐҩѧУÓУ¨ÖÐÒ©·ÖÎöÓë¼ø¶¨£©×¨Òµ£¬ÄÇËùѧУҪºÃµã£¬Ð»Ð»
ÒѾÓÐ38È˻ظ´
¡¾ÇóÖú¡¿ÄÄλÊÖÉÏÓÐCuOºÍCu2OÔÚ2000K-3000KµÄÈÈÁ¦Ñ§Êý¾Ý
ÒѾÓÐ3È˻ظ´

Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¶¹Þ¢-Ä껪: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл°¡£¡ 2013-08-18 13:25:35
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¶¹Þ¢-Ä껪: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл°¡£¡ 2013-08-18 13:25:35
|
1 . compound 20 C25H41O6 ÏàËÆ¶È:56% Journal of Asian Natural Products Research 2006 8 545-554 An attempt to enlarge the B ring of maoecrystal B,an ent-kaurane-type diterpene L. XU and F.-P. WANG Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . methyl 17-hydroxyhomodaphniphyllate C23H37NO3 ÏàËÆ¶È:54.1% Helvetica Chimica Acta 2007 Vol. 90 2156 Alkaloids from the Fruits of Daphniphyllum macropodum Xiao-Ning Wang, Li-She Gan, Cheng-Qi Fan, Sheng Yin, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (12S)-7¦Á-acetoxy-18-chloro-15,16-epoxyneocleroda-13(16),14-dien-20,12-olide 4¦Á,6¦Á,19-Orthoacetate C24H29O8Cl ÏàËÆ¶È:54.1% Journal of Natural Products 1996 59 367-373 Chemical Transformations of the Neoclerodane Diterpenes Eriocephalin and Capitatin: An Access to 4, 5-seco-Neoclerod-5(19)-ene Derivatives1 Ekkehard Mössner, 2 Maria C. de la Torre, and Benjamin Rodriguez Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 8 ÏàËÆ¶È:54.1% Chemical & Pharmaceutical Bulletin 1980 28 365-371 Carbon-13 Nuclear Magnetic Resonance Spectral Assignments of Grayanotoxin-I NAOHIRO SHIRAI,HISAO NAKATA,TOYO KAIYA and JINSAKU SAKAKIBARA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (13S,14R)-14-Acetoxy-6¦Â-methoxy-17-trimethylsilyloxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androstan-17-carbonitrile ÏàËÆ¶È:54.1% Steroids 2004 69 501-509 Synthesis of 13,14-secotestosterone derivatives Vladimir A. Khripach, Vladimir N. Zhabinskii, Anna I. Kuchto, Yuliya Y. Zhiburtovich, Galina P. Fando, Alexander S. Lyakhov, Alla A. Govorova, Marinus B. Groen, Jaap van der Louw, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . rabdosichuanin D C24H34O8 ÏàËÆ¶È:54.1% Phytochemistry 1990 29 2591-2595 Diterpenoids from Rabdosia setschwanensis Huang Hao,Zhang Hongjie,Sun Handong Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 5¦Á-Bromo-3¦Â-formyloxy-18-iodo-6,19-oxidopregnan-20-one C22H30O4 ÏàËÆ¶È:54.1% Steroids 1996 61 345-348 Synthesis of oxido-bridged analogs of 18-hydroxyprogesterone M. O. Violeta Benedetti Doctorovich, Alberto A. Ghini, Gerardo Burton Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Á-aminodigoxigenin C23H36NO4 ÏàËÆ¶È:54.1% Steroids 1996 61 562-564 A straightforward synthesis of 3¦Á- and 3¦Â-aminodigoxigenin Maciej Adamczyk, Jonathan Grote Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 20¦Â-( tert-butyidimethybtlyioxy)-5¦Á-pregnane-13¦Â,14¦Â-diol 3-acetate C29H52O4Si ÏàËÆ¶È:54.1% Steroids 1993 58 518-523 Synthesis and structure-activity relationships of 14¦Â-hydroxy-5¦Á-pregnanes: pregnanes that bind to the cardiac glycoside receptor John F. Templeton, Yangzhi Ling, V.P.Sashi Kumar, Frank S. LaBella Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 2 ÏàËÆ¶È:54.1% Journal of the Chemical Society, Perkin Transactions 1 1975 1502-1506 Structure and synthesis of a new ketone from Cedrus species; some new constituents of C. atlantica Manet David R. Adams, Surendra P. Bhatnagar and Richard C. Cookson Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (1R,1'R,2S,5R)-5-methyl-2-methylethylcyclohexyl 2'-(3'',4''-methylenedioxyphenyl)cyclohex-2'-enylcarbamate C24H33NO4 ÏàËÆ¶È:54.1% Australian Journal of Chemistry 1994 47 2235-2254 Convergent Routes to the [1,3]Dioxolo[4,5-j]phenanthridin-6(5H)-one and 2,3,4,4a-Tetrahydro[1,3]dioxolo[4,5-j]phenanthridin-6(5H)-one Nuclei. Application to Syntheses of the Amaryllidaceae Alkaloids Crinasiadine, N-Methylcrinasiadine and Trisphaeridine MG Banwell and CJ Cowden Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (1R,1'S,2S,5R)-5-methyl-2-methylethylcyclohexyl 2'-(3'',4''-methylenedioxyphenyl)cyclohex-2'-enylcarbamate C24H33NO4 ÏàËÆ¶È:54.1% Australian Journal of Chemistry 1994 47 2235-2254 Convergent Routes to the [1,3]Dioxolo[4,5-j]phenanthridin-6(5H)-one and 2,3,4,4a-Tetrahydro[1,3]dioxolo[4,5-j]phenanthridin-6(5H)-one Nuclei. Application to Syntheses of the Amaryllidaceae Alkaloids Crinasiadine, N-Methylcrinasiadine and Trisphaeridine MG Banwell and CJ Cowden Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 13 C22H33NO5 ÏàËÆ¶È:54.1% Indian Journal of Chemistry 1997 36B 682-684 Preparation of imine alkaloids from nor-diterpenoids alkaloids Liming Gao, Shangzhen Zheng, Xiaojiang Hao, Xiaoxiong Wang & Xuwei Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 8 ÏàËÆ¶È:54.1% Chinese Journal of Organic Chemistry 2008 28 1264-1267 Chemical Component Studies of the South China Sea Gorgonian Muricella Sinensis YAN, Xiao-Hong LI, Zhen-Yu GUO, Yue-Wei* Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 4-methyl-2-(6-trifluoromethyl-1,3-oxazinan-3-yl)-pentanoic acid methyl ester C12H20F3NO3 ÏàËÆ¶È:54.1% Journal of the Brazilian Chemical Society 2005 16 1255-1261 Synthesis of N-Substituted 6-Trifluoromethyl-1,3-oxazinanes Nilo Zanatta, Adriana M. C. Squizani, Leonardo Fantinel, Fabiane M. Nachtigall, Deise M. Borchhardt, Helio G. Bonacorso and Marcos A. P. Martins Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ËÄ´¨Ïã²è²Ë¶¡ËØ C24H34O8 ÏàËÆ¶È:54.1% Chinese Traditional and Herbal Drugs 2012 43 247-250 Studies on diterpenoids from Rabdosia nervosa WEI Zhi-xiong; GAO You-heng; LU Hai-xiao; HOU Yuan-fang; LIU Sha; LI Shu-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 2 C26H42O8 ÏàËÆ¶È:53.8% Chemical & Pharmaceutical Bulletin 1990 38 1743-1744 Sweet and Bitter Diterpene-Glucosides from Leaves of Rubus suavissimus Satomi HIRONO,Wen-Hua CHOU,Ryoji KASAI,Osamu TANAKA and Toshiharu TADA Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-08-18 12:27:34














»Ø¸´´ËÂ¥