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13C NMR (101 MHz, CDCl3) ¦Ä 14.65,15.15,16.19,17.21,17.54,18.48,28.73,29.69,30.17,35.91,35.96,45.96,48.91,208.38,212.92 |
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mrdone.0907: ½ð±Ò+20, ¡ïÓаïÖú 2013-10-25 13:20:35
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mrdone.0907: ½ð±Ò+20, ¡ïÓаïÖú 2013-10-25 13:20:35
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²éѯ½á¹û£º¹²²éµ½55¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 15 ÏàËÆ¶È:60% Phytochemistry 1998 47 1577-1581 Sesquiterpenoids from Cyperus rotundus Susumu Ohira, Taisuke Hasegawa, Ken-Ichiro Hayashi, Takuji Hoshino, Daisuke Takaoka, Hiroshi Nozaki Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound(part ref 98) ÏàËÆ¶È:60% Phytochemistry 1994 37 597-623(605) The daucane (carotane) class of sesquiterpenes Emilio L. Ghisalberti Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 10 ÏàËÆ¶È:60% Tetrahedron Letters 2002 43 221-224 Synthesis of the napalilactone and pathylactone A spirocyclic skeleton James R. Vyvyan, Courtney A. Rubens, Jason A. Halfen Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (5R,6S,7S,10S)-7-isopropyl-10-methyl-6-trimethylsilyloxyspiro[4.5]decan-2-one C17H32O2Si ÏàËÆ¶È:60% Tetrahedron 2005 61 10853-10860 Silicon guided rearrangement of epoxydecalines to spirocyclic compounds. Synthesis of gleenol and axenol from carvone Gonzalo Blay, Ana M. Collado, Begoña Garc¨ªa, Jos¨¦ R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Gibberosin A C19H28O3 ÏàËÆ¶È:57.8% Bulletin of the Chemical Society of Japan 2006 79 1547-1551 New ¦Â-Caryophyllene-Derived Terpenoids from the Formosan Soft Coral Sinularia gibberosa Shin-Pin Chen, Chih-Hua Chao, Ho-Cheng Huang, Yang-Chang Wu, Chung-Kuang Lu, Chang-Feng Dai, Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (R)-di-tert-butyl 1-(2-methyl-1-oxopentan-2-yl)hydrazine-1,2-dicarboxylate ÏàËÆ¶È:56.2% Tetrahedron 2013 69 5438-5443 ¦Â-tert-Butyl aspartate as an organocatalyst for the asymmetric ¦Á-amination of ¦Á,¦Á-disubstituted aldehydes Alexis Theodorou, Giorgos N. Papadopoulos, Christoforos G. Kokotos Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 14,15-dinorclerod-3-ene-2,13-dione C18H28O2 ÏàËÆ¶È:55.5% Helvetica Chimica Acta 2003 Vol. 86 3187 Dinorditerpene, Diterpenes, Alkaloids, and Coumarins from Clausena dunniana Hong-Ping He, Yue-Mao Shen, Guo-Ying Zuo, Xiao-Sheng Yang, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (4aR,7R,8S,8aR)-4,4a,7,8-tetramethyl-8-(3-oxobutyl)-4a,5,6,7,8,8a-hexahydronaphthalen-2(1H)-one C18H28O2 ÏàËÆ¶È:55.5% Zeitschrift f¨¹r Naturforschung B 2007 62b 577-579 A Novel Norditerpene from Eupatorium adenophorum Ming-ZhongWang, Xiang-Hai Cai, Guo-Shun Du, and Xiao-Dong Luo Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (1R,3aR,5S,7aR)-5-Azido-1-((R)-1,5-dimethylhexyl)-3a,7a-dimethyloctahydroinden-4-one ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2013 21 1925-1943 Stereoselective synthesis of a new class of potent and selective inhibitors of human ¦¤8,7-sterol isomerase Mathias König, Christoph M¨¹ller, Franz Bracher Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Gibberosin E C20H30O2 ÏàËÆ¶È:55% Bulletin of the Chemical Society of Japan 2006 79 1547-1551 New ¦Â-Caryophyllene-Derived Terpenoids from the Formosan Soft Coral Sinularia gibberosa Shin-Pin Chen, Chih-Hua Chao, Ho-Cheng Huang, Yang-Chang Wu, Chung-Kuang Lu, Chang-Feng Dai, Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (10¦Â)-10-Hydroxyaristolan-9-one C15H24O2 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2007 Vol. 90 385 Aristolane Sesquiterpenes and Highly Brominated Indoles from the Marine Red Alga Laurencia similis (Rhodomelaceae) Nai-Yun Ji, Xiao-Ming Li, Lan-Ping Ding, and Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . elongatol B C15H22O3 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2007 55(5) 762-765 Nardosinane Sesquiterpenoids from the Formosan Soft Coral Nephthea elongata Shang-Kwei WANGa and Chang-Yih DUH Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-deoxypseudoanisatin C15H22O5 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2004 52(1) 104-107 Seven Novel seco-Prezizaane-Type Sesquiterpenes from the Pericarps of Illicium merrillianum Jian-Mei HUANG,Chun-Shu YANG,Ren ZHAO,Hironobu TAKAHASHI,and Yoshiyasu FUKUYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (1S,4S,5S,6R,7S,10S)-dihydroxymaaliane C15H26O2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2000 48(11) 77-80 Three New Sesquiterpenoid Glucosides of Ficus pumila Fruit Junichi KITAJIMA,Kaoru KIMIZUKA,and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (1S,10S)-9¦Â-Hydroxy-allo-aromadendrane C15H26O ÏàËÆ¶È:53.3% 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 16 . compound 9 ÏàËÆ¶È:53.3% Journal of Natural Products 2005 68 1208-1212 Oxygenated Terpenoids from a Formosan Soft Coral Sinularia gibberosa Atallah F. Ahmed, Yao-Haur Kuo, Chang-Feng Dai, and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . aristolan-10-ol-9-one C15H24O2 ÏàËÆ¶È:53.3% Chinese Chemical Letters 2007 18 178-180 Two new aristolane sesquiterpenes from Laurencia similis Nai Yun Ji, Xiao Ming Li, Lan Ping Ding, Bin Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 4¦Á,7¦Â-Dihydroxyeudesmane C15H28O2 ÏàËÆ¶È:53.3% Journal of Asian Natural Products Research 2006 8 723-731 Eudesmane-type sesquiterpenoids from the liverwort Lepidozia fauriana H.-S. SHY and C.-L. WU Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . japodic acid C13H22O3 ÏàËÆ¶È:53.3% Records of Natural Products 2008 2 100-106 Japodic acid, A Novel Aliphatic Acid from Jatropha podagrica Hook Olapeju O. Aiyelaagbe and James B. Gloer Structure 13C NMR ̼Æ×Ä£Äâͼ |
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