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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£º¹²²éµ½175¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3,7-dimethyloct-1-ene-3,6,7-triol ÏàËÆ¶È:90% Chemical & Pharmaceutical Bulletin 1999 47 639-642 Monoterpenoid Glucosides of Cnidium monnieri Fruit Junichi KITAJIMA,Yoshie AOKI,Toru ISHIKAWA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (3S,6S)-6,7-dihydroxy-6,7-dihydrolinalool C10H20O3 ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 2003 51 32-39 Water-Soluble Constituents of Coriander Toru Ishikawa, Kyoko Kondo and Junichi Kitajima Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (3S,6R)-6,7-dihydroxy-6,7-dihydrolinalool C10H20O3 ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 2003 51 32-39 Water-Soluble Constituents of Coriander Toru Ishikawa, Kyoko Kondo and Junichi Kitajima Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . trans-linalool oxide ÏàËÆ¶È:70% Phytochemical Analysis 1998 9 10-13 Stereoisomeric flavour compounds. LXXVIII. Separation and structure elucidation of the pyranoid linalool oxide stereoisomers using common gas chromatographic phases, modified cyclodextrin phases and nuclear magnetic resonance spectroscopy Barbara Weinert, Matthias W¨¹st, Armin MosandL and Helmut Hanssum Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 6-vinyl-3¦Á-hydroxy-2,2,6¦Á-trimethyltetrahydropyran ÏàËÆ¶È:70% Russian Journal of Organic Chemistry 2002 38 498-506 Rearrangements of Epoxides of Linalool and Nerolidyl Acetate in Acid Media T. M. Khomenko, L. E. Tatarova, D. V. Korchagina and V. A. Barkhash Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1-cyclohexyl-2-nitroethanol ÏàËÆ¶È:70% European Journal of Organic Chemistry 2010 5190-5196 Indium-Mediated Reaction of 1-Bromo-1-nitroalkanes with Aldehydes: Access to 2-Nitroalkan-1-ols Raquel G. Soengas and Amalia M. Est¨¦vez Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . [(3S,6R)-6-ethenyl-3-hydroxy-2,2,6-trimethyltetrahydropyran ÏàËÆ¶È:70% Flavour and Fragrance Journal 2004 19 275-280 Epoxidation¨Ccyclization of rosewood oxides Isabelle Bombarda, Lionel Cezanne and Emile M. Gaydou Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (1S,2S,3R,4R)-4-(tert-butoxymethyl)-2,3-(isopropylidenedioxy)cyclopentan-1-ol ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 2010 18 3403-3412 Structure¨Cactivity relationships of carbocyclic 6-benzylthioinosine analogues as subversive substrates of Toxoplasma gondii adenosine kinase Young Ah Kim, Ravindra K. Rawal, Jakyung Yoo, Ashoke Sharon, Ashok K. Jha, Chung K. Chu, Reem H. Rais, Omar N. Al Safarjalani, Fardos N.M. Naguib, Mahmoud H. el Kouni Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3,7-dimethyloct-3(10)-ene-1,6,7-triol C10H20O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1999 47 805-808 Water-Soluble Constituents of Fennel. VIII.Monoterpenoid Alcoho |

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