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| 13C NMR (101 MHz, CDCl3) ¦Ä13.33,23.56,27.30,29.69,34.28,35.46,37.27,68.65,125.24,140.34, 199.30. |
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fangfuhu123: ½ð±Ò+10, ¡ïÓаïÖú 2015-06-06 00:09:21
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fangfuhu123: ½ð±Ò+10, ¡ïÓаïÖú 2015-06-06 00:09:21
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²éѯ½á¹û£º¹²²éµ½108¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 76 ÏàËÆ¶È:83.3% Journal of Agricultural and Food Chemistry 1990 38 1041-1048 Two-dimensional GC-DCCC analysis of the glycoconjugates of monoterpenes, norisoprenoids, and shikimate-derived metabolites from Riesling wine Peter Winterhalter, Mark A. Sefton, Patrick J. Williams Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 9-Hydroxy-5,7-megastigmadien-4-one ÏàËÆ¶È:83.3% Journal of Tropical and Subtropical Botany 2010 18 564-568 Chemical Constituents from Isodon lophanthoides var. gracilif lora LIANG, Yao, guang, XU, Xinya, XIE, Hai, hui, LIN, Qing, WEI, Xiao, yi Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (4R)-1-bromo-4-methyldecane C11H23Br ÏàËÆ¶È:63.6% European Journal of Organic Chemistry 2011 5894-5904 Synthesis of Optically Pure Diglycerol Tetraether Model Lipids with Non-Natural Branching Pattern Thomas Markowski, Simon Drescher, Annette Meister, Gerd Hause, Alfred Blume and Bodo Dobner Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-methyloctanol ÏàËÆ¶È:63.6% Natural Product Communications 2013 8 869-871 Structural Factors in the Odor of ¦Á-Santalol Derivatives Toshio Hasegawa, Hiroaki Izumi and Hideo Yamada Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (7E,9¦Î)-9-hydroxy-5,7-megastigmadien-4-one C13H20O2 ÏàËÆ¶È:61.5% Phytochemistry 2004 65 497-505 Structure elucidation and phytotoxicity of C13 nor-isoprenoids from Cestrum parqui Brigida D¡¯Abrosca, Marina DellaGreca, Antonio Fiorentino, Pietro Monaco,Palma Oriano, Fabio Temussi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . cytotoxic sesquiterpene caryol-7-en-6-ol ÏàËÆ¶È:60% Helvetica Chimica Acta 2009 92 375-378 A New Tricyclo[6.3.1.02,5]dodecane Sesquiterpene from Cultures of the Basidiomycete Campanella junghuhnii Rong Liu, Zhong-Yu Zhou, Di Xu, Fei Wang, Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . sesquiterpene C15H24O ÏàËÆ¶È:60% Australian Journal of Chemistry 1988 41 1755-1761 Sesquiterpenes From a New Zealand Sponge of the Genus Eurypon CJ Barrow, JW Blunt and MHG Munro Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . isofurocaespitane C12H16OBrCl ÏàËÆ¶È:58.3% Tetrahedron letters 1979 20 2719-2722 Carbon-13 NMR application to Laurencia polyhalogenated sesquiterpenes A.G. Gonz¨¢lez, J.D. Mart¨ªn, V.S. Mart¨ªn, M. Norte Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (R)-3-Methyloctyl-4-methylbenzenesulfonate ÏàËÆ¶È:57.1% Chemistry of Natural Compounds 2010 46 440-443 Stereoselective synthesis of the sex pheromone of the yellow mealworm using (S)-4-benzyloxazolidinone as chiral auxiliary D. L. Li, C. F. Lu, G. C. Yang and Z. X. Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (2E,4R,5S)-2-ethylidene-5-(methoxycarbonyl)-4-methylhexano-5-lactone C11H16O4 ÏàËÆ¶È:54.5% Helvetica Chimica Acta 2007 Vol. 90 1028 Sesquiterpenoids and Lactone Derivatives from Ligularia dentata Hitomi Baba, Yasunori Yaoita, and Masao Kikuchi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ((5-butyltetrahydrofuran-2-yl)ethynyl)trimethylsilane(Major isomer) C19H24OSi ÏàËÆ¶È:54.5% Organic Letters 2007 Vol. 9, No. 10 1975-1978 Ene-yne Tetrahydrofurans from the Sponge Xestospongia muta. Exploiting a Weak CD Effect for Assignment of Configuration Brandon I. Morinaka, Colin K. Skepper, and Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ((5-butyltetrahydrofuran-2-yl)ethynyl)trimethylsilane(Minor isomer) C19H24OSi ÏàËÆ¶È:54.5% Organic Letters 2007 Vol. 9, No. 10 1975-1978 Ene-yne Tetrahydrofurans from the Sponge Xestospongia muta. Exploiting a Weak CD Effect for Assignment of Configuration Brandon I. Morinaka, Colin K. Skepper, and Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . N-Ethylpiperidin-4-ylmethyl valerate C13H25NO2 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry Letters 2004 14 1927-1930 N-[18F]fluoroethylpiperidin-4-ylmethyl butyrate: a novel radiotracer for quantifying brain butyrylcholinesterase activity by positron emission tomography Tatsuya Kikuchi, Ming-Rong Zhang, Nobuo Ikota, Kiyoshi Fukushi, Toshimitsu Okamura, Kazutoshi Suzuki, Yasushi Arano, Toshiaki Irie Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (4aS,8S )-4a-methyl-8- hydroxy-4 ,4a,5,6,7,8-hexahydro-2(3 H )naphthalenone ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry Letters 1997 7 587-592 Regio- and stereoselective aspects in the oxidation of (R) and (S) 4a-methyl-(4,4a,5,6,7,8)-hexahydro-2(3H)naphthalenones in living rats Philippe V¨¦rit¨¦, Sabine M¨¦nager, Christian Cav¨¦, Dominique Andr¨¦, Jean d'Angelo, Gilbert Revial, Claude Combet Farnoux, Olivier Lafont Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (2S,6R)-2,6-Dimethyl-1,8-octanediol ÏàËÆ¶È:54.5% Chemistry of Natural Compounds 2010 46 305-307 Chemical constituents from Incarvillea delavayi Yun-Heng Shen, Tao Lu, Jian Tang, Run-Hui Liu and Hui-Liang Li, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (R)-4-Methylnonanenitrile ÏàËÆ¶È:54.5% Chemistry of Natural Compounds 2010 46 440-443 Stereoselective synthesis of the sex pheromone of the yellow mealworm using (S)-4-benzyloxazolidinone as chiral auxiliary D. L. Li, C. F. Lu, G. C. Yang and Z. X. Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 4,4a,5,6,7,8-Hexahydronaphthalen-2(3H)-one C10H14O ÏàËÆ¶È:54.5% Zeitschrift f¨¹r Naturforschung B 2005 60 984-989 Synthesis of Decaline Analogues of Isovelleral M. Johansson, I. Aujard, D. Röme, H. Anke, and O. Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ethyl(Z)-6-methyl-4-octenoate C11H20O2 ÏàËÆ¶È:54.5% Tetrahedron 1993 49 6569-6574 Isolation and synthesis of caprolactins A and B, new caprolactams from a marine bacterium Bradley S. Davidson, Robert W. Schumacher Structure 13C NMR ̼Æ×Ä£Äâͼ |

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