| ²é¿´: 729 | »Ø¸´: 3 | ||
æëÀÀľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Íò·Ö¸Ðл ÒÑÓÐ1È˲ÎÓë
|
|
̼Æ×Êý¾Ý£º141.66,139.61,130.84,129.27,72.35,72.28,69.97,65.12,64.98,63.95,45.86,45.48,44.01,40.98,38.11,37.92,35.38,29.83,29.12,28.04,27.93,27.81,27.78,22.43,22.23,21.98,15.66,15.59 ÈܼÁ£º¼×´¼ ÏàËÆ¶È£º´óÓÚ70 |
» ²ÂÄãϲ»¶
310Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏÓ뻯¹¤328·Öµ÷¼Á
ÒѾÓÐ8È˻ظ´
318Ò»Ö¾Ô¸¼ªÁÖ´óѧÉúÎïÓëÒ½Ò© Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸ÄÏ¿ª´óѧ0710ÉúÎïѧ359Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ4È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
309Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸ÄϺ½ 335·Ö | 0856 | GPA 4.07 | ÓпÆÑоÀú
ÒѾÓÐ8È˻ظ´
Çó»¯Ñ§µ÷¼Á
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
8΢Æ×ÇóÖú£¬Ð»Ð»¡£
ÒѾÓÐ3È˻ظ´
¶Ï¿Ú·ÖÎöÇóÖú£¬·Ç³£½ô¼±Íò·Ö¸Ðл
ÒѾÓÐ14È˻ظ´
΢Æ×ÇóÖú£¬¸Ðл£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Íò·Ö¸Ðл
ÒѾÓÐ3È˻ظ´
ÇóάÆÕ£¬Íò·Ö¸Ðл¡£
ÒѾÓÐ4È˻ظ´
ÃÌËáï®XPSÊý¾Ý·ÖÎöÇóÖú£¡£¡Íò·Ö¸Ðл£¡
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»¾§Ìå ÊÇ·ñ±¨µÀ¹ý¾§ÌåÊý¾Ý£¬Íò·Ö¸Ðл£¡
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
XÉäÏß¹âµç×ÓÄÜÆ× XPSÊý¾Ý·ÖÎöÇóÖú£¡£¡¼±£¡Íò·Ö¸Ðл£¡
ÒѾÓÐ8È˻ظ´
Çó´óϺ²é΢Æ×£¬Íò·Ö¸Ðл°¡£¡£¡£¡
ÒѾÓÐ3È˻ظ´
JMC paper Ͷ¸åÖ¸ÄÏÇóÖú£¬ Íò·ÖÆÚ´ý£¡£¡£¡
ÒѾÓÐ7È˻ظ´
ÇóÈË΢Æ×²éѯ£¬¼±£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú£ºÇó½Ì£ºµÂ¹ÌÈü Degussa P25 Íò·Ö¸Ðл~~£¡
ÒѾÓÐ15È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
2Â¥2013-12-11 16:54:28
æëÀÀ
ľ³æ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 2011.6
- É¢½ð: 32
- Ìû×Ó: 157
- ÔÚÏß: 103Сʱ
- ³æºÅ: 2223083
- ×¢²á: 2013-01-05
- רҵ: Ò©Îﻯѧ
3Â¥2013-12-11 20:58:55
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
æëÀÀ: ½ð±Ò+15, ¡ïÓаïÖú 2013-12-12 14:46:08
æëÀÀ: ½ð±Ò+15, ¡ïÓаïÖú 2013-12-12 14:46:08
|
²éѯ½á¹û£º¹²²éµ½401¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . nicaphysalin A ÏàËÆ¶È:60.7% Chemical & Pharmaceutical Bulletin 1994 42 318-321 Five New Ergostane-Related Compounds from Nicandra physaloides Kazushi SHINGU,Shoji YAHARA and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 3¦Â,6¦Á-diacetoxy-9¦Á,11¦Á-dihydroxy-5¦Á-pregn-7-ene-20(S)-carbaldehyde ethylene acetal ÏàËÆ¶È:60.7% Natural Product Research 2001 15 221-228 Short Synthesis of Novel 9,11-Secosterols Raissa Jäälaid; Ivar Järving; Tõnis Pehk; Omar Parve; Ülo Lille Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 12¦Á-Chloro-9¦Á,11¦Á-epoxy-5¦Á-stigmastan-3¦Â-ol C29H49ClO2 ÏàËÆ¶È:60.7% European Journal of Organic Chemistry 1993 1993 657-663 Pheromone Synthesis, CLI. Synthesis of Chlorinated Steroids Related to the Structures Proposed for Blattellastanosides A and B, the Aggregation Pheromone of the German Cockroach, Blattella germanica L. Kenji Mori, Kunio Fukamatsu and Masaru Kido Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . sodium sulfate C29H49O6SNa ÏàËÆ¶È:58.6% Chemistry of Natural Compounds 1986 22 411-415 STEROID COMPOUNDS OF MARINE SPONGES.VII. PREPARATION OF DERIVATIVES OF SOKOTRASTEROL AND HALISTANOL SULFATES AND STRUCTURE-ACTIVITY INTERRELATIONSHIPS AMONG THESE COMPOUNDS T. N. Makar'eva, I. A. Gorshkova, B. A. Gorshkov, A. I. Kalinovskii, and V. A. Stonik Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . dehyahsapogenin ÏàËÆ¶È:58.6% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . dehydrosapogenin ÏàËÆ¶È:58.6% Phytochemistry 1984 23 639-644 Noroleanane saponins from Celmisia petriei Daryl D. Rowan, Roger H. Newman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . abeohyousterone C27H42O5 ÏàËÆ¶È:57.1% Journal of Natural Products 2007 70 1859-1864 Ecdysteroids from the Antarctic Tunicate Synoicum adareanum Yoshinari Miyata,Thushara Diyabalanage,Charles D. Amsler, James B. McClintock, Frederick A. Valeriote, and Bill J. Baker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (22R)-9,11-secochlolest-3¦Â,9¦Â,11,22-tetraol C27H50O4 ÏàËÆ¶È:57.1% Steroids 2010 75 834-847 Synthesis of cytotoxic novel 9,11-secosterol analogs: Structure/activity studies Boonsong Kongkathip, Anuch Hasakunpaisarn, Suthinee Boonananwong, Ngampong Kongkathip Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 2¦Á,5¦Á-Diacetoxy-10¦Â,11-epoxy-14-oxo-taxa-4(20),12(13)-diene C24H32O6 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 2011 59(8) 1038-1041 Biotransformation of a Taxadiene by Ginkgo Cell Cultures and the Tumor Multi-Drug Resistant Reversal Activities of the Metabolites Dan XIE, Yi ZHANG, Jianhua ZOU, Dali YIN, Xiaoguang CHEN, and Jungui DAI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3¦Â-28-dihydroxy-18-1upene ÏàËÆ¶È:56.6% Chemistry of Natural Compounds 1989 25 557-564 OXIDATION OF TRITERPENES DERIVED FROM 18-LUPENE AND 18,19- SECOLUPANE WITH RUTHENIUM TETROXIDE BY AN IMPROVED PROCEDURE M. V. Denisenko, L. E. Odinokova, and N. I. Uvarova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (20S,24R)3¦Â,20,21¦Â,25-tetrahydroxy-21,24-cyclodammarane C30H52O4 ÏàËÆ¶È:56.6% Chinese Chemical Letters 2011 22 1461-1464 Two new dammarane-type sapogenins from Gynostemma pentaphyllum Xia Li,Jia Qing Cao,Lin Shi,Yu Qing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 13¦Â-Hydroxy-7¦Á, 27-oxy-12-dihydro-18¦Â-glycyrrhetinic acid ÏàËÆ¶È:56.6% Phytochemistry 2010 71 262-270 Bioactive microbial metabolites from glycyrrhetinic acid Galal T. Maatooq, Amani M. Marzouk, Alexander I. Gray, John P. Rosazza Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 3 C32H54O6 ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 1980 28 473-478 Studies on Marine Natural Products. II. New Polyhydroxylated Sterols from the Soft Coral Lobophytum pauciflorum (Ehrenberg) YASUJI YAMADA,SUKEJI SUZUKI,KAZUO IGUCHI,HIROYUKI KIKUCHI,YASUMASA TSUKITANI,HARUO HORIAI and HAJIME NAKANISHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 2¦Á,3¦Á,19¦Á-trihydroxy-24-norurs-4(23),12-dien-28-oic acid C29H44O5 ÏàËÆ¶È:55.1% Chemical & Pharmaceutical Bulletin 2005 53(12) 1594-1596 24-nor-Ursane Type Triterpenoids from the Stems of Rumex japonicus Dae Sik JANG,Jong Min KIM,Joo-Hwan KIM,and Jin Sook KIM Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 24-ethyl-3¦Â,6¦Â-dihydroxycholest-22-ene disulfate ÏàËÆ¶È:55.1% Steroids 2009 74 1057-1060 Synthesis and cytotoxic analysis of some disodium 3¦Â,6¦Â-dihydroxysterol disulfates Jianguo Cui, Hui Wang, Yanmin Huang, Yi Xin, Aimin Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . maragenin II ÏàËÆ¶È:55.1% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Ajugamarin B1 ÏàËÆ¶È:55.1% Phytochemical Analysis 2002 13 372-380 NMR shift data of neo-clerodane diterpenes from the genus Ajuga Josep Coll Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . maragenin (II) ÏàËÆ¶È:55.1% Phytochemistry 1984 23 639-644 Noroleanane saponins from Celmisia petriei Daryl D. Rowan, Roger H. Newman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . haliclonacyclamine C C32H58N2 ÏàËÆ¶È:55.1% Tetrahedron 1998 54 8811-8826 The haliclonacyclamines, cytotoxic tertiary alkaloids from the tropical marine sponge Haliclona sp Richard J. Clark, Kim L. Field, Romila D. Charan, Mary J. Garson, M. Brereton, Anthony C. Willis Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 2-{2-[3-(acetamidomethyl)benzylamino]-2-oxoethoxy}-N,N-dioctylacetamide C30H51N3O4 ÏàËÆ¶È:55.1% European Journal of Organic Chemistry 2011 3959-3969 Hydrolysis and Radiation Stability of m-Xylylene Bis-diglycolamide: Synthesis and Quantitative Study of Degradation Products by HPLC¨CAPCI+ Hitos Gal¨¢n, Mar¨ªa Teresa Murillo, Rosa Sedano, Ana N¨²ñez, Javier de Mendoza, Amparo Gonz¨¢lez-Espartero and Pilar Prados Structure 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2013-12-12 09:14:41














»Ø¸´´ËÂ¥