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1 . muurolane-4¦Â,5¦Â,10¦Â-triol C15H28O3 ÏàËÆ¶È:68.7% Chemical & Pharmaceutical Bulletin 2003 51(8) 986-989 Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (()-3,7,11-trimethyl-1,7,11-dodecanetriol C15H32LiO3 ÏàËÆ¶È:68.7% Journal of Natural Products 2002 65 1319-1322 African Elephant Sesquiterpenes. II. Identification and Synthesis of New Derivatives of 2,3-Dihydrofarnesol Thomas E. Goodwin,Felisia D. Brown, Richard W. Counts, Nichole C. Dowdy, Patrick L. Fraley,Randall A. Hughes, Daniel Z. Liu, Courtney D. Mashburn, Josh D. Rankin, Russell S. Roberson, Katie D. Wooley, Elizabeth L. Rasmussen, Scott W. Riddle, Heidi S. Ridd Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . pterodondiol C15H28O2 ÏàËÆ¶È:68.7% 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 -------------------------------------------------------------------------------- 4 . 1R,3S,6S,7R,10S-7-Isopropyl-4,10-dimethylbicyclo[4.4.0]dec-4-en-3,10-diol C15H26O2 ÏàËÆ¶È:68.7% Chemistry of Natural Compounds 2002 38 154-160 SYNTHESIS OF THE ELEUTHESIDE CORE FROM (+)-d-CADINOL:CONSTRUCTION OF SIDE CHAINS ON THE MENTHANE RING I. P. Tsypysheva, A. M. Kunakova, O. V. Shitikova,L. V. Spirikhin, F. A. Valeev, and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Pterodondiol ÏàËÆ¶È:68.7% 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 -------------------------------------------------------------------------------- 6 . 1¦Â,4¦Â,5¦Á-trihydroxy-6¦Â-acetoxyeudesmane C17H30O5 ÏàËÆ¶È:68.7% Journal of Natural Products 1988 Vol 51 475 Epoxidation Reaction of 6¦Â-Acetoxyeudesmenes and Acid-catalyzed Transformations of the Epoxy Compounds E. Cabrera, A. Garcia-Granados, M. A. Quecuty Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . pterodondiol ÏàËÆ¶È:68.7% Chinese Pharmaceutical Journal 1995 30 264-265 Chemical study on Laggera pterodonta Zhao Aihua, Zhu Yan, Wei Junxian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . cadinane-4¦Â,5¦Á,10¦Á-triol C15H28O3 ÏàËÆ¶È:68.7% Planta Medica 2012 78 1010-1014 Sesquiterpenoids from the Rhizomes of Homalomena occulta Xie, Xiao-Yu; Wang, Rui; Shi, Yan-Ping: Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . acetylation of cadinanetriol C17H28O3 ÏàËÆ¶È:64.7% Planta Medica 1997 63 250-254 Minor Components with Smooth Muscle Relaxing Properties from Scented Myrrh (Commiphora guidotti) Maria Andersson, Ola Bergendorff, Rudong Shan, Peter Zygmunt, and OIov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 12-epilycodoline N-oxide C16H25NO3 ÏàËÆ¶È:62.5% Helvetica Chimica Acta 2004 Vol. 87 1963 Lycopodine-Type Lycopodium Alkaloids from Huperzia serrata Chang-Heng Tan and Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . cadinane-4¦Â,5¦Á,10¦Â-triol C15H28O3 ÏàËÆ¶È:62.5% Chemical & Pharmaceutical Bulletin 2003 51(8) 986-989 Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (-)1¦Â,4¦Â,6¦Átrihydroxy-eudesmane C15H28O3 ÏàËÆ¶È:62.5% Phytochemistry 2008 69 2367-2373 Sesquiterpenoids from Homalomena occulta affect osteoblast proliferation,differentiation and mineralization in vitro Yong-Mei Hu, Chuan Liu, Ka-Wing Cheng, Herman H.-Y. Sung, Lan D. Williams,Zhong-Lin Yang Wen-Cai Ye Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (1S,10S)-9¦Á-hydroxy-allo-aromadendrane C15H26O ÏàËÆ¶È:62.5% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (1R,4R,5R,8S,9S,13S)-caryolane-5,8,13-triol C15H26O3 ÏàËÆ¶È:62.5% Journal of Natural Products 2006 69(10) 1429-1434 Microbial Transformation and Butyrylcholinesterase Inhibitory Activity of (− -Caryophyllene Oxide and Its DerivativesMuhammad Iqbal Choudhary, Zafar A. Siddiqui, Sarfraz A. Nawaz, and Atta-ur-Rahman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . compound 3 ÏàËÆ¶È:62.5% Journal of Natural Products 2002 65 1319-1322 African Elephant Sesquiterpenes. II. Identification and Synthesis of New Derivatives of 2,3-Dihydrofarnesol Thomas E. Goodwin,Felisia D. Brown, Richard W. Counts, Nichole C. Dowdy, Patrick L. Fraley,Randall A. Hughes, Daniel Z. Liu, Courtney D. Mashburn, Josh D. Rankin, Russell S. Roberson, Katie D. Wooley, Elizabeth L. Rasmussen, Scott W. Riddle, Heidi S. Ridd Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (4Z,8¦Á,11S)-caryophyll-4(5)-ene-8,14-diol C15H26O2 ÏàËÆ¶È:62.5% Journal of Natural Products 2000 63 44-47 Biotransformation of (4E,8R)-Caryophyll-4(5)-en-8-ol by Botrytis cinerea Rosa Dur¨¢n-Patr¨®n, Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (4Z,3S,8R)-caryophyll-4(5)-ene-3,8-diol C15H26O2 ÏàËÆ¶È:62.5% Journal of Natural Products 2000 63 44-47 Biotransformation of (4E,8R)-Caryophyll-4(5)-en-8-ol by Botrytis cinerea Rosa Dur¨¢n-Patr¨®n, Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 7¦ÂH-eudesm-2-ene-4¦Á,11-diol C15H26O2 ÏàËÆ¶È:62.5% 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 -------------------------------------------------------------------------------- 19 . 4¦Â,5¦Á, 10¦Â-trihydroxycadinane C15H26O2 ÏàËÆ¶È:62.5% Planta Medica 1997 63 250-254 Minor Components with Smooth Muscle Relaxing Properties from Scented Myrrh (Commiphora guidotti) Maria Andersson, Ola Bergendorff, Rudong Shan, Peter Zygmunt, and OIov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . pterodontriol B ÏàËÆ¶È:62.5% Acta Botanica Yunnanica 1994 16(3) 313-314 THE STRUCTURE OF PTERODONTETRAOL FROM LAGGERA PTERODONTA LI Shun-Lin, DING Jing-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . pterodontetraol C15H28O4 ÏàËÆ¶È:62.5% Acta Botanica Yunnanica 1994 16(3) 313-314 THE STRUCTURE OF PTERODONTETRAOL FROM LAGGERA PTERODONTA LI Shun-Lin, DING Jing-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . pterodontriol A C15H28O3 ÏàËÆ¶È:62.5% 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 -------------------------------------------------------------------------------- 23 . pterodontriol B Cl5H28O3 ÏàËÆ¶È:62.5% 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 -------------------------------------------------------------------------------- 24 . ent-oplopanone C15H26O2 ÏàËÆ¶È:62.5% Chemical & Pharmaceutical Bulletin 1987 35 124-135 Marine Natural Products. XVII. Nephtheoxydiol, a New Cytotoxic Hydroperoxy-Germacrane Sesquiterpene, and Related Sesquiterpenoids from an Okinawan Soft Coral of Nephthea sp. (Nephtheidae) ISAO KITAGAWA,ZHENG CUI,BYENG WHA SON,MOTOMASA KOBAYASHI and YOSHIMASA KYOGOKU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . laggerone A C15H26O3 ÏàËÆ¶È:62.5% Chinese Chemical Letters 1996 7 1093-1094 EUDESMANES AND EUDESMANOIC GLUCOSIDES FROM LAGGERA PETERODONTA YU ZHAO,JIAN MIN YUE,JING KAI DING,ZHONG WEN LIN AND HAN DONG SUN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . Pterodontriol B ÏàËÆ¶È:62.5% 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 -------------------------------------------------------------------------------- 27 . oplopanone C15H26O4 ÏàËÆ¶È:62.5% Natural Product Research 2003 17 445-449 A new xanthone from Hedychium gardnerianum Maria João Carvalho; Lu¨ªs M. Carvalho; Ana Margarida Ferreira; Artur M. S. Silva Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2013-01-21 18:58:35













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-Caryophyllene Oxide and Its Derivatives