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zhiwu1983(¶¹¸ç´ú·¢): ½ð±Ò+15, лл 2013-10-16 08:13:08
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zhiwu1983(¶¹¸ç´ú·¢): ½ð±Ò+15, лл 2013-10-16 08:13:08
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²éѯ½á¹û£º¹²²éµ½603¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 1¦Â,11-dihydroxy-5-eudesmene ÏàËÆ¶È:100% Phytochemistry 2004 65 127-137 ent-Clerodane diterpenes and other constituents from the liverwort Adelanthus lindenbergianus (Lehm.) Mitt. Barbara Blä s, Josef Zapp, Hans Becker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 6 ÏàËÆ¶È:100% The Journal of Organic Chemistry 1983 48 4410-4413 An aristolane sesquiterpenoid from the sea pen Scytalium splendens Muu N. Do, Karen L. Erickson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 1¦Â-hydroxy-11-methoxy-5-eudesmene ÏàËÆ¶È:66.6% Phytochemistry 2004 65 127-137 ent-Clerodane diterpenes and other constituents from the liverwort Adelanthus lindenbergianus (Lehm.) Mitt. Barbara Blä s, Josef Zapp, Hans Becker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 4,10-epoxy-muuralan-5-ol C15H26O2 ÏàËÆ¶È:66.6% Journal of Natural Products 1999 62 549-553 Muurolane Sesquiterpenes from Illicium tsangii Koon-Sin Ngo, Wing-Tak Wong, and Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 5¦Á-Hydroperoxy-¦Â-eudesmol C15H26O3 ÏàËÆ¶È:66.6% Molecules 2003 8 670-677 Sesquiterpenes from Cymbopogon proximus Hesham I. El-Askary, Meselhy R. Meselhy and Ahmed M. Galal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . rosifoliol C15H26O ÏàËÆ¶È:66.6% Tetrahedron letters 1977 18 873-876 Biogenetically significant sesquiterpenoids from Rubus rosifolius oil Ian A. Southwell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (1R,3S,6R,7R,8R,11S)-11-iodo-6-isopropyl-1,3-dimethyl-2-oxatricyclo[5.3.1.0(3,8)]undecane ÏàËÆ¶È:66.6% Russian Journal of Organic Chemistry 2004 40 337-345 Functionalization of the Allyl Fragment in (+)-¦Ä-Cadinol F. A. Valeev, I. P. Tsypysheva, A. M. Kunakova, O. Yu. Krasnoslobodtseva and O. V. Shitikova, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . rosifoliol ÏàËÆ¶È:66.6% Australian Journal of Chemistry 1978 31 2527-2538 The Constituents of Rubus rosifolius. The Structure of Rosifoliol, a Biogenetically Significant Sesquiterpenoid I Southwell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (1S,2S)-Di-(-)-menthyl Cyclohex-4-ene-1,2-dicarboxylate ÏàËÆ¶È:66.6% Journal of Medicinal Chemistry 1989 32 197-202 Synthesis and biological evaluation of a monocyclic, fully functional analog of compactin Clayton H. Heathcock, Brian R. Davis, Cheri R. Hadley Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 8 ÏàËÆ¶È:66.6% The Journal of Organic Chemistry 1983 48 4410-4413 An aristolane sesquiterpenoid from the sea pen Scytalium splendens Muu N. Do, Karen L. Erickson Structure 13C NMR ̼Æ×Ä£Äâͼ |
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