| ²é¿´: 216 | »Ø¸´: 1 | ||
wangsanÒø³æ (СÓÐÃûÆø)
|
[ÇóÖú]
άÆ×ÇóÖú
|
| 75.0,74.2,49.9,49.2,41.1,35.0,34.8,31.6,30.7,25.1,22.5,20.4,19.5,19.4,17.9 |
» ²ÂÄãϲ»¶
»·¾³×¨Ë¶µ÷¼Á
ÒѾÓÐ7È˻ظ´
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´
22408 µ÷¼Á²ÄÁÏ
ÒѾÓÐ6È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ19È˻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
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
wangsan: ½ð±Ò+5, ¡ïÓаïÖú 2013-11-18 17:49:38
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
wangsan: ½ð±Ò+5, ¡ïÓаïÖú 2013-11-18 17:49:38
|
²éѯ½á¹û£º¹²²éµ½360¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Tricyclohumuladiol C15H26O2 ÏàËÆ¶È:80% Journal of Asian Natural Products Research 2005 7 847-852 Chemical constituents from Schisandra plena R.-T. LI, A.-H. ZHAO, Y.-H. SHENG, Z. NA and H.-D. SUN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . tricyclohumuladiol ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2005 36 1619-1620 ÏÁ°êӥצ»¨µÄ±¶°ëÝÆÀà³É·ÖÑо¿ ³Â¹âÓ¢;Öì¹úÔª;º«³¤ÈÕ;ÀîÇìÑó;·½ºêÑ«;±ÏºÍƽ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 14 C15H26O ÏàËÆ¶È:66.6% Phytochemistry 1997 46 1203-1208 Terpenoids from the Japanese liverworts Jackiella javanica and Jungermannia infusca Fumihiro Nagashima, Akiko Tamada, Noriko Fujii, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Teucdiol A C15H26O2 ÏàËÆ¶È:66.6% Phytochemistry 1993 34 1083-1086 Eudesmane sesquiterpenes from Teucrium heterophyllum. The x-ray structure of teucdiol a Braulio M. Fraga, Melchor G. Hern¨¢ndez, Teresa Mestres, Jos¨¦ M. Arteaga, Aurea Perales Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 4-acetoxy-3,15-dinor-2,3-seco-2-africanone C15H24O2 ÏàËÆ¶È:66.6% Journal of Chemical Research 2000 24 48-50 Unusual terpenoid constituents of the soft coral Sinularia dissecta Ramesh, P.; Venkateswarlu, Y. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 7 C16H26O3 ÏàËÆ¶È:66.6% Journal of Medicinal Chemistry 1984 27 1367-1369 Synthesis of a tricyclic aphidicolin analog which inhibits DNA synthesis in vitro John E. McMurry, Thomas R. Webb Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 5¦Á-bromo-6¦Â-hydroxyandrost-17-one C19H29O2Br ÏàËÆ¶È:63.1% Steroids 1998 63 62-69 Reaction of androst-5-en-17-one with hypobromous acid and its use for synthesis of 19-oxygenated 5-ene and 4-en-6-one steroids Mitsuteru Numazawa, Keiko Yamada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (11S)-4¦Â,6¦Â,11,12-tetrahydroxyeudesman-1-one C15H26O5 ÏàËÆ¶È:60% Journal of Natural Products 2002 65 1011-1015 Chemical-Microbiological Synthesis of Cryptomeridiol Derivatives by Gliocladium roseum: Semisynthesis of 11-Hydroxyeudesmanolides Andr¨¦s Garc¨ªa-Granados, Mar¨ªa C. Guti¨¦rrez, Andr¨¦s Parra, and Francisco Rivas Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 7¦ÂH-eudesmane-3¦Á,4¦Á,11-triol C15H28O3 ÏàËÆ¶È:60% Journal of Natural Products 1998 61 22-28 Enantioselective Total Syntheses of (-)-7¦ÂH-Eudesmane-4¦Á, 11-diol and (+)-ent-7¦ÂH-Eudesmane-4¦Á, 11-diol Fumito Shimoma, Hisao Kondo, Saori Yuuya, Toshio Suzuki, Hisahiro Hagiwara, and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 12 ÏàËÆ¶È:60% Journal of Natural Products 1997 60 1026-1030 Sesquiterpene Glycosides and Phenylpropanoid Esters from Phonus arborescens (Carthamus arborescens) Alejandro F. Barrero, Pilar Arteaga, Jos¨¦F. Qu¨ªlez, Ignacio Rodr¨ªguez, and M. Mar Herrador Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . aristoian-9¦Â-ol ÏàËÆ¶È:60% Planta Medica 1987 53 556-558 Gansongon, a New Aristolane Ketone from Nardostachys chinesis and Structure Revision of an Aristolenol Luo Shide, A. Olbrich, R. Mayer and G. RUcker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (1S,2S,3R,6R,7R)-Epoxy-himachal-7-ol ÏàËÆ¶È:60% Molecules 2001 6 M228 (1S, 2S, 3R, 6R, 7R)-Epoxy-himachal-7-ol M. Dakir, E. Lassaba, A. Chekroun and A. Benharref Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 1¦Â,6¦Á,8¦Â-triacetoxy-9¦Á-benzoyloxy-¦Â-agarofuran ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2003 5 205-208 A NEW SESQUITERPENE ESTER FROMTHE FRUITS OF CELASTRUS ORBICULATUS YUAN-QIANG GUO, XIAN LI, JIN-HUI WANG, WEN LI and YI SHA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . tricyclo[6.3.1.0(2.5)]dodecane-6¦Á,8¦Á-diol C15H26O ÏàËÆ¶È:60% Journal of Natural Products 1990 Vol 53 1353 Chemistry of Sponges, X. New Sesquiterpenes from a Marine Sponge of the Genus Eurypon M. R. Kernan, R. C. Cambie, Patricia R. Bergquist Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (+)-4-muurolen-6¦Á-ol C15H26O ÏàËÆ¶È:60% Phytochemistry 1994 37 1323-1325 Cadinane-type sesquiterpenoids from the liverwort Scapania undulata Fumihiro Nagashima, Keiko Suda, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (+)-4-muurolen-6¦Á-ol C15H26O ÏàËÆ¶È:60% Phytochemistry 1994 37 1323-1325 Cadinane-type sesquiterpenoids from the liverwort Scapania undulata Fumihiro Nagashima, Keiko Suda, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . kessane ÏàËÆ¶È:60% Phytochemistry 1993 33 857-862 Cis-dihydroagarofuran from Prostanthera sp. aff. ovalifolia Ian A. Southwell, David J. Tucker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (¡À)-norzizanone ÏàËÆ¶È:60% Tetrahedron Letters 2000 41 10353-10356 A stereocontrolled total synthesis of (¡À)-norzizanone Lokesh Chandra Pati, Arnab Roy, Debabrata Mukherjee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 3¦Â,4¦Â-dihydroxypallenone C15H36O3 ÏàËÆ¶È:60% Phytochemistry 1990 29 3355-3358 Dihydroxypallenone,a sesquiterpene with a new carbon skeleton from Pallenis spinosa A.A. Ahmed,J. Jakupovic,F. Bohlmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . Senecrassidiol C15H24O2 ÏàËÆ¶È:60% Phytochemistry 1981 20 469-472 Sesquiterpenes from three Senecio species Ferdinand Bohlmann, J¨¹rgen Ziesche Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . Teucdiol A |
2Â¥2013-11-18 07:51:33














»Ø¸´´ËÂ¥