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BY-16 CÆ× ÈܼÁ£ºÂÈ·Â 17.59,22.52,27.33,29.48,30.24,30.29,30.82,32.14,38.76,41.62,43.09,47.11,65.17,120.30,141.59 |
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Stephanie88: ½ð±Ò+10, ¡ïÓаïÖú 2015-06-15 23:06:47
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Stephanie88: ½ð±Ò+10, ¡ïÓаïÖú 2015-06-15 23:06:47
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²éѯ½á¹û£º¹²²éµ½44¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (+)-5-epi-aristolochene ÏàËÆ¶È:73.3% Phytochemistry 1990 29 479-482 Synthesis of (+)-5-epi-aristolochene and (+)-1-deoxycapsidiol from capsidiol Ian M. Whitehead,David F. Ewing,David R. Threlfall,David E. Cane,P.C. Prabhakaran Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (4R,5R,9S,10S,11S)-Morel-2-ene C15H24 ÏàËÆ¶È:66.6% Journal of Natural Products 2004 67 189-193 Preparation of Moreliane-Derived Volatile Sesquiterpenes Carlos M. Cerda-Garca-Rojas, Mara A. Bucio, Luisa U. Romn, Juan D. Hernndez, and Pedro Joseph-Nathan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 10¦Â,13-Dihydroxy-marasm-7 (8)-en-5-oic acid ¦Ã-lactone C15H20O3 ÏàËÆ¶È:66.6% Phytochemistry 1996 41 1093-1096 Monohydroxylactones of Lactarius vellereus Wodzimierz M. Daniewski, Maria Gumuka, Dorota Truszewska, Ulla Jacobsson, Torbjorn Norin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Debneyol C15H24O ÏàËÆ¶È:66.6% Phytochemistry 1985 24 2191-2194 Debneyol, a fungicidal sesquiterpene from tnv infected Nicotiana debneyi R.S. Burden, P.M. Rowell, J.A. Bailey, R.S.T. Loeffler, M.S. Kemp, C.A. Brown Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 2 ÏàËÆ¶È:66.6% Phytochemistry 1985 24 2195-2200 Sesquiterpenoid phytoalexins from suspended callus cultures of Nicotiana tabacum David G. Watson, David S. Rycroft, Isabel M. Freer, Charles J.W. Brooks Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . debneyol ÏàËÆ¶È:66.6% Phytochemistry 1986 25 1607-1608 Cyclodebneyol, a fungitoxic sesquiterpene from TNV infected Nicotiana debneyi R.S. Burden, R.S.T. Loeffler, P.M. Rowell, J.A. Bailey, M.S. Kemp Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 1¦Á-Hydmxy-1-epiprobotrydial ÏàËÆ¶È:66.6% Journal of Chemical Ecology 1994 20 2631-2644 Synthesis and antifungal activity of analogues of naturally occurring botrydial precursors Isidro G. Collado, Josefina Aleu, Antonio J. Mac¨ªas-S¨¢nchez, Rosario Hern¨¢ndez-Gal¨¢n Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . cadina-1(10)-ene C15H26 ÏàËÆ¶È:60% Phytochemistry 2007 68 587-590 A sesquiterpene hydrocarbon from the bogwoods of Cryptomeria japonica D. Don, presumably formed by diagenetic hydrogenation Hiroe Narita, Kazuo Furihata, Shigenori Kuga, Mitsuyoshi Yatagai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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