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| 13C NMR (600MHz,±ûͪ):21.23,27.34,27.68,27.77,34.07,39.40,68.46,71.39,124.90,135.90. |
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ħÁ¦Äñ: ½ð±Ò+15, ¡ïÓаïÖú 2014-07-25 11:02:15
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ħÁ¦Äñ: ½ð±Ò+15, ¡ïÓаïÖú 2014-07-25 11:02:15
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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£º¹²²éµ½190¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . myrseguinoside A aglycone C10H18O2 ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 2011 59(10) 1274-1280 Myrseguinosides A-E, Five New Glycosides from the Fruits of Myrsine seguinii Katsuyoshi MATSUNAMI, Hideaki OTSUKA, and Yoshio TAKEDA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 51 ÏàËÆ¶È:70% Organic Magnetic Resonance 1975 7 426-432 13C-NMR-Spektren von Monoterpenen F. Bohlmann, R. Zeisberg and E. Klein Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (4aS*,8aR*)-4a-Hydroxymethyl-1,2,4a,5,6,7,8,8a-octahydro-2-naphthol C11H18O2 ÏàËÆ¶È:63.6% Journal of the Chemical Society, Perkin Transactions 1 1996 1523-1529 Chemistry of insect antifeedants from Azadirachta indica(part 21): synthesis of model compounds of azadirachtin using a decalin framework as a functional group scaffolding Mar¨ªa L. de la Puente, Steven V. Ley, Monique S. J. Simmonds and Wally M. Blaney Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (+)-¦Â-ambrinol ÏàËÆ¶È:61.5% Flavour and Fragrance Journal 2013 28 46-52 An expedient preparation of enantio-enriched ambergris odorants starting from commercial ionone alpha Stefano Serra Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (1S,2S,4R)-p-menthane-8-ene-1,2-diol ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2002 50 501-507 Water-Soluble Constituents of Dill Toru Ishikawa, Masato Kudo and Junichi Kitajima Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (1S,2S,4R)-p-menth-8-ene-1,2-diol ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2002 50 66-72 Water-Soluble Constituents of Caraway: Carvone Derivatives and Their Glucosides Tetsuko Matsumura, Toru Ishikawa and Junichi Kitajima Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 6 ÏàËÆ¶È:60% Tetrahedron Letters 2005 46 7867-7870 Synthesis of N-substituted 2,4-thiazolidinediones from oxazolidinethiones Guadalupe Mendoza, Hector Hern¨¢ndez, Leticia Quintero, Martha Sosa-Rivadeneyra, Sylvain Bern¨¨s, Estibaliz Sansinenea, Aurelio Ortiz Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . rel-(1S,2S,4R,8S)-p-menthane-2,8,9-triol C10H20O3 ÏàËÆ¶È:60% Tetrahedron 2001 57 8067-8074 New p-menthanetriols and their glucosides from the fruit of caraway Tetsuko Matsumura, Toru Ishikawa, Junichi Kitajima Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . rel-(1S,2S,4R,8R)-p-menthane-2,8,9-triol C10H20O3 ÏàËÆ¶È:60% Tetrahedron 2001 57 8067-8074 New p-menthanetriols and their glucosides from the fruit of caraway Tetsuko Matsumura, Toru Ishikawa, Junichi Kitajima Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (1S,5R,6S)-2,6-dimethyl-8-oxabicyclo[3.3.1]non-2-en-4-ol C10H16O2 ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2011 47 989-993 Skeletal rearrangements of cis-(-)-7,8-epoxycarveol derivatives promoted by triethylsilyl trifluoromethanesulfonate S. A. Torosyan, F. A. Gimalova, A. A. Fatykhov, M. R. Talipov and R. F. Valeev, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 2 ÏàËÆ¶È:60% Australian Journal of Chemistry 1991 44 77-85 Norterpene Dienes From an Australian Marine Sponge Latrunculia brevis MS Butler and RJ Capon Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 3 ÏàËÆ¶È:60% Australian Journal of Chemistry 1994 47 1509-1521 2,9-Dihydroxy- and 2,10-Dihydroxy-1,8-cineole. Two New Possum Urinary Metabolites RM Carman, AC Garner and KD Klika Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3¦Â-hydroxy-cis-¦Â-terpineol C10H18O2 ÏàËÆ¶È:60% Natural Product Communications 2007 2 969-976 Phytochemical Investigations of an Antitubercular Extractof Chilean Myrcianthes coquimbensis and Related Populations Smriti Khera, Gloria Montenegro and Barbar Timmermann Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 4-cis-hydroxy-hydroxy-2e-methyl-4-ethynyl-trans-decahydroquinoline ÏàËÆ¶È:58.3% Russian Journal of Organic Chemistry 2002 38 1116-1124 Synthesis and Reactions of 4-cis- and 4-trans-Hydroxy-2e-methyl-4-ethynyl-trans-decahydroquinolines S. S. Koval'skaya, N. G. Kozlov and E. A. Dikusar Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 7 ÏàËÆ¶È:54.5% Tetrahedron Letters 2003 44 6519-6521 Sulfur ylides generated from the reaction of adamantylidene and phenylcarbene with sulfur substrates Yuri N Romashin, Michael T.H Liu, Brian T Hill, Matthew S Platz Structure 13C NMR ̼Æ×Ä£Äâͼ |

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