| ²é¿´: 210 | »Ø¸´: 1 | ||
hejiangboľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×²éѯ
|
|
ÈܼÁ£º¼×´¼ ÏàËÆ¶È£º90%ÒÔÉÏ ºË´ÅÊý¾Ý£º 14.4,20.6,23.5,29.8,36.1,36.7,39.7,40.6,47.7,60.0,60.7,64.7,76.8,106.9,155.6 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ17È˻ظ´
302·ÖÇóµ÷¼Á Ò»Ö¾Ô¸°²»Õ´óѧ085601
ÒѾÓÐ12È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ23È˻ظ´
»·¾³×¨Ë¶µ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 µ÷¼Á²ÄÁÏ
ÒѾÓÐ6È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ19È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÕæµÄͦ²»´íµÄ£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
journal of molecular structureͶ¸åÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
¼±¼±¼±¡£¡£¡£¡£ÇóÖú΢Æ×Êý¾Ý£¨50%ÏàËÆ¶È¾ÍOKÁË£©£¬²»Ê¤¸Ðл£¡
ÒѾÓÐ8È˻ظ´
΢Æ×²é½á¹¹ лл
ÒѾÓÐ3È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖú΢Æ×²éѯ½âÆ×
ÒѾÓÐ5È˻ظ´

ÓÐËù²»Îª
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 304 (´óѧÉú)
- ½ð±Ò: 9684.2
- É¢½ð: 16
- ºì»¨: 14
- Ìû×Ó: 1106
- ÔÚÏß: 814.3Сʱ
- ³æºÅ: 481441
- ×¢²á: 2007-12-17
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hejiangbo: ½ð±Ò+10 2013-12-05 12:16:01
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hejiangbo: ½ð±Ò+10 2013-12-05 12:16:01
|
²éѯ½á¹û£º¹²²éµ½135¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (7¦Á)-8-oxoeudesm-4(14)-en-12-oic acid C15H22O3 ÏàËÆ¶È:60% Helvetica Chimica Acta 2007 Vol. 90 1586 Cadinane and Eudesmane Sesquiterpenoids from Chloranthus henryi Bin Wu, Shan He, Xiao-Dan Wu, De-Kang Wu, and Yuan-Jiang Pan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Xylaranic acid C15H24O5 ÏàËÆ¶È:60% Helvetica Chimica Acta 2010 93 796-802 Four New Terpenoids from Xylaria sp. 101 Yao-Yao Li, Zhi-Yu Hu, Chun-Hua Lu and Yue-Mao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (2E,9E)-6,7-dibromo-2,9-humuradien-8-one C15H22OBr2 ÏàËÆ¶È:60% The Journal of Organic Chemistry 1999 64 2667-2672 Chemistry of Zerumbone. 1. Simplified Isolation, Conjugate Addition Reactions, and a Unique Ring Contracting Transannular Reaction of Its Dibromide Takashi Kitayama and Tadashi Okamoto, Richard K. Hill, Yasushi Kawai and Sho Takahashi, Shigetomo Yonemori, Yukio Yamamoto, Kouichi Ohe and Sakae Uemura, Seiji Sawada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 13 ÏàËÆ¶È:60% Indian Journal of Chemistry Section B 2000 39B 42-56 Two new terpenoid derivatives from a new soft coral species of the Nephthea genus of the India ocean A S R Anjaneyulu, M V R Krishna Murthy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (+)-(3aR,5S,5aS,9aS,9bR)-3a,6,6,9a-tetramethyldodecahydronaphtho[2,1-b]furan-5-yl methanesulfonate C17H30O4S ÏàËÆ¶È:58.8% Tetrahedron 2001 57 5663-5679 The synthesis of Ambrox®-like compounds starting from (+)-larixol Marjon G Bolster, Ben J.M Jansen, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 14 C18H32O3 ÏàËÆ¶È:58.8% European Journal of Organic Chemistry 2010 1483-1493 Synthetic Studies Directed Towards Various Homologues of Natural Sesquiterpene-Coumarin Ethers: The Domino Approach Andrei Corbu, Juan M. Castro, Maurizio Aquino, Zoila Gandara, Pascal Retailleau and Sim¨¦on Arseniyadis Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . compound 6 ÏàËÆ¶È:56.2% Phytochemistry 1996 42 771-774 A tetranorfriedolabdane diterpene from Vellozia stipitata Ângelo C. Pinto, Octavio A. C. Antunes, Moacir G. Pizzolatti, Victor M. Rumjanek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 24a C16H24O4 ÏàËÆ¶È:56.2% Tetrahedron Letters 2004 45 383-386 Carbanion cyclisation of esters. Part 2: Enantiospecific construction of the tricyclic framework of the marine sesquiterpenes, spirodysins A. Srikrishna, P. Ravi Kumar, S.S.V. Ramasastry Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . tetrahydroakagerine ÏàËÆ¶È:55.5% Australian Journal of Chemistry 1993 46 969-976 The Alkaloids of Ophiorrhiza cf. ferruginea D Arbain, NH Lajis, DP Putra, MV Sargent, BW Skelton and AH White Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . spiramilactone C C20H28O4 ÏàËÆ¶È:55% Phytochemistry 1998 48 1213-1215 Diterpenes from Spiraea japonica Xiao-Jiang Hao, Jing-Lei Nie Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 11 ÏàËÆ¶È:55% Phytochemistry 1991 30 2991-3000 Diterpenes and norditerpenes from the Aristeguetia group C. Zdero, F. Bohlmann, R.M. King Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (1S,3¦ÁR,4- S,8¦ÁS,9R)-Decahydro-4,8,8-trimethyl-1,4-methanoazulene-9-carboxylic Acid ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2003 Vol. 86 106 The Ozonolysis of Longifolene: A Tool for the Preparation of Useful Chiral Compounds. Configuration Determination of New StereogenicCenters by NMR Spectroscopy and X-Ray Crystallography Vladimir Dimitrov, Gudrun Hopp Rentsch, Anthony Linden, and Manfred Hesse Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . alismol ÏàËÆ¶È:53.3% Phytochemistry 2003 63 877-881 Guaiane-type sesquiterpenoids from Alisma orientalis Guo-Ping Peng, Gang Tian, Xian-Feng Huang, Feng-Chang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . nardosinanol H C14H23O4 ÏàËÆ¶È:53.3% Journal of Natural Products 2008 71(3) 375-380 Nardosinanols A#I and Lemnafricanol, Sesquiterpenes from Several Soft Corals, Lemnalia sp., Paralemnalia clavata, Lemnalia africana, and Rhytisma fulvum fulvum Ashgan Bishara, Dina Yeffet, Mor Sisso, Guy Shmul, Michael Schleyer, Yehuda Benayahu, Amira Rudi, and Yoel Kashman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . cyperusol D C15H24O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2004 67 569-576 Structures of New Sesquiterpenes and Hepatoprotective Constituents from the Egyptian Herbal Medicine Cyperus longus Fengming Xu, Toshio Morikawa, Hisashi Matsuda, Kiyofumi Ninomiya, and Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 3¦Â-Hydroxyeudesma-1,11(13)-dieno-12,6¦Â-lactone C15H20O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2003 66 810-817 Synthetic Method and Biological Activities of cis-Fused ¦Á-Methylene ¦Ã-Lactones Yohsuke Higuchi, Fumito Shimoma, and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . subergorgiol C15H24O ÏàËÆ¶È:53.3% Journal of Natural Products 2002 65 1033-1036 Two New Subergane-Based Sesquiterpenes from a Taiwanese Gorgonian Coral Subergorgia suberosa Guey-Horng Wang, Atallah F. Ahmed, Yao-Haur Kuo, and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 2¦Â-hydroxysubergorgic acid ÏàËÆ¶È:53.3% Journal of Natural Products 2002 65 1033-1036 Two New Subergane-Based Sesquiterpenes from a Taiwanese Gorgonian Coral Subergorgia suberosa Guey-Horng Wang, Atallah F. Ahmed, Yao-Haur Kuo, and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (4R,5R,8S)-4,5-epoxycaryophyllan-8-ol C15H26O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 41-44 Biotransformation of Caryophyllene Oxide by Botrytis cinerea Rosa Duran, Elena Corrales, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 2-¦Â-hydroxysubergorgic acid C15H22O3 ÏàËÆ¶È:53.3% Journal of Natural Products 1998 61 832-834 Studies on the Secondary Metabolites from the Indian Gorgonian Subergorgia suberosa: Isolation and Characterization of Four Analogues of the Cardiotoxin Subergorgic Acid P. S. Parameswaran, C. G. Naik, S. Y. Kamat, M. S. Puar, P. Das, and Vinod R. Hegde Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . compound 10 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1994 42 2430-2435 Crude Drugs from Aquatic Plants. V. On the Constituents of Alismatis Rhizoma. (3). Stereostructures of Water-Soluble Bioactive Sesquiterpenes, Sulfoorientalols a, b, c, and d, from Chinese Alismatis Rhizoma Masayuki YOSHIKAWA,Shoko YAMAGUCHI,Hisashi MATSUDA,Nobumitsu TANAKA,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . (1S,10S),(4S,5S)-germacrone-1(10),4-diepoxide C15H22O3 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1991 39 843-853 A Series of Sesquiterpenes with a 7¦Á-Isopropyl Side Chain and Related Compounds Isolated from Curcuma wenyujin Kenzo HARIMAYA,Ji-Fu GAO,Tamiko OHKURA,Takeshi KAWAMATA,Yoichi IITAKA,Yong-Tian GUO and Seiichi INAYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . wenjine |

2Â¥2013-12-05 12:07:07














»Ø¸´´ËÂ¥