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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½412¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (-)-7¦ÂH-eudesmane-4¦Á,11-diol C15H28O2 ÏàËÆ¶È:100% 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 2 . Pterodondiol ÏàËÆ¶È:100% Journal of Asian Natural Products Research 2007 9 277-283 Sesquiterpenoids from Hedychium yunnanense and Porana discifera, and the structural revision of two sesquiterpenoids from Laggera pterodonta W.-M. ZHU, Q. ZHAO, S.-L. LI and X.-J. HAO Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 4,5-epi-cryptomeridiol C15H26O ÏàËÆ¶È:100% Journal of Natural Products 1992 Vol 55 730 Three New Eudesmane Sesquiterpenes from Pluchea arguta Viqar Uddin Ahmad, Tanveer Ahmed Farooqui, Kaniz Fizza, Azra Sultana, Rasheeda Khatoon Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 4,5-epi-cryptomeridiol ÏàËÆ¶È:100% Journal of Natural Products 1994 Vol 57 1189 Synthetic Studies of Sesquiterpenes with a cis-Fused Decalin System, 4. Synthesis of (+)-5¦ÂH-Eudesma-3,11-diene, (-)-5¦ÂH-Eudesmane-4¦Â,11-diol, and (+)-5¦ÂH-Eudesmane-4¦Á,11-diol, and Structure Revision of a Natural Eudesmane-4,11-diol Isolated from Pluchea Masayoshi Ando, Koji Arai, Kazuhira Kikuchi, Koji Isogai Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 4¦Â,11-¶þôÇ»ù-¶ÔÓ³èñÍé C15H28O2 ÏàËÆ¶È:100% Chinese Pharmaceutical Journal 1995 30 264-265 Chemical study on Laggera pterodonta Zhao Aihua, Zhu Yan, Wei Junxian Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound X ÏàËÆ¶È:100% Heterocycles 2001 54 765-776 Intramolecular Photocycloaddition of 2-Cycloalkenyl-1,3-dioxin-4-one. Stereoselective Synthesis of cis-Eudesmane-4,11-diols Toshihide Hatsui,* Ka Li, Akira Mori,* and Hitoshi Takeshita Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . pterodondiol C15H28O2 ÏàËÆ¶È:86.6% Acta Botanica Yunnanica 1993 15(3) 303-305 THREE NEW SESPUITERPENOLS FROM LAGGERA PTERODONTA LI Shun-Lin, DING Jing-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Pterodondiol ÏàËÆ¶È:86.6% Journal of Asian Natural Products Research 2007 9 277-283 Sesquiterpenoids from Hedychium yunnanense and Porana discifera, and the structural revision of two sesquiterpenoids from Laggera pterodonta W.-M. ZHU, Q. ZHAO, S.-L. LI and X.-J. HAO Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 4¦Â,11-dihydroxy-10-epi-eudesmane C15H26O ÏàËÆ¶È:86.6% Phytochemistry 1992 31 863-880 Sesquiterpene lactones and other constituents from Ursinia species J. Jakupovic, U. Ganzer, P. Pritschow, L. Lehmann, F. Bohlmann, R.M. King Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . pterodondiol ÏàËÆ¶È:86.6% Chinese Pharmaceutical Journal 1995 30 264-265 Chemical study on Laggera pterodonta Zhao Aihua, Zhu Yan, Wei Junxian Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 7¦ÂH-eudesmane-3¦Á,4¦Á,11-triol C15H28O3 ÏàËÆ¶È:80% 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 12 . compound 15 ÏàËÆ¶È:66.6% 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 13 . 3-methyl-5-(2,2,6-trimethyl-6-hydroxy-cyclohexyl)-pentanoic acid ÏàËÆ¶È:66.6% Planta Medica 2002 68 808-812 Antimicrobial Terpenoids from the Oleoresin of the Peruvian Medicinal Plant Copaifera paupera Benigna M.Tincusi,Ignacio A.Jim¨¦nez,Isabel L.Bazzocchi,Laila M.Moujir,Zulma A.Mamani,Jos¨¦P.Barroso,Angel G.Ravelo,Basilio V.Hern¨¢ndez Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . pterodontriol A C15H28O3 ÏàËÆ¶È:66.6% Acta Botanica Yunnanica 1993 15(3) 303-305 THREE NEW SESPUITERPENOLS FROM LAGGERA PTERODONTA LI Shun-Lin, DING Jing-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ |

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