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NO.1 13.054, 18.046, 23.941, 29.981, 30.888, 34.414, 42.455, 44.270, 67.720, 71.847, 215.319 frp-14a ë®´úÂÈ·Â |
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À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2014-04-09 18:28:05
bababa416: ½ð±Ò+10, лл 2014-04-09 21:45:21
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À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2014-04-09 18:28:05
bababa416: ½ð±Ò+10, лл 2014-04-09 21:45:21
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²éѯ½á¹û£º¹²²éµ½87¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4-Octyloxetan-2-one ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 1998 6 1255-1272 Synthesis and inhibitory action on HMG-CoA synthase of racemic and optically active oxetan-2-ones (¦Â-Lactones) Daniel Romo, Paul H.M. Harrison, Stephen I. Jenkins, R.William Riddoch, Kaapjoo Park, Hong Woon Yang, Cunxiang Zhao, Gerard D. Wright Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (¡À)- and meso-7,11-dimethylheptadecane-7,11-diol ÏàËÆ¶È:63.6% European Journal of Organic Chemistry 2004 2004 1198-1201 Synthesis and Enantioselective Gas Chromatography of Stereoisomers of 7,11-Dimethylheptadecane − A Pheromone Component of Lambdina Species Sharon Chow, Wilfried A. Koenig and William Kitching Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (5S,7S)-7-hydroxy-5-dodecanolide C12H20O2 ÏàËÆ¶È:58.3% European Journal of Organic Chemistry 2002 2002 3884-3892 Absolute Configuration and Synthesis of ¦Â- and ¦Ä-Lactones Present in the Pheromone System of the Giant White Butterfly Idea leuconoe Katja Stritzke,Stefan Schulz,and Ritsuo Nishida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 1-hydroxydecane-2,5-dione C10H18O3 ÏàËÆ¶È:54.5% Journal of Natural Products 2008 71(8) 1423-1426 Sesquiterpenes and Aliphatic Diketones from Cultures of the Basidiomycete Conocybe siliginea Zhong-Yu Zhou, Jian-Guo Tang, Fei Wang, Ze-Jun Dong, and Ji-Kai Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 5-Ethylnonan-4-one C11H22O ÏàËÆ¶È:54.5% Journal of Natural Products 2006 69 863-870 Ethyl-Branched Aldehydes, Ketones, and Diketones from Caimans (Caiman and Paleosuchus; Crocodylia, Reptilia) Karsten Krckert, Birte Flachsbarth, Stefan Schulz, Ute Hentschel, and Paul J. Weldon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . compoung 2 C8H17O4S ÏàËÆ¶È:54.5% Journal of Natural Products 1996 59 271-272 A New Iodinated Metabolite and a New Alkyl Sulfate from the Senegalese Sponge Ptilocaulis spiculifer Moussoukhoye Diop, Abdoulaye Samb, Valeria Costantino, Ernesto Fattorusso, and Alfonso Mangoni Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 7 C10H20O2 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 1981 29 1636-1643 The Constituents of Schizonepeta tenuifolia BRIQ. I. Structures of Two New Monoterpene Glucosides, Schizonepetosides A and B HIROSHI SASAKI,HEIHACHIRO TAGUCHI,TOHRU ENDO,ITIRO YOSIOKA and YOICHI IITAKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . cis-2,5,6-Trimethyl-l-cyclohexene-l-carbaldeh ÏàËÆ¶È:54.5% Helvetica Chimica Acta 1980 63 293-314 Synthesis and Configuration of the Eight Diastereoisomeric Racemates of Dactyloxene-B. The relative configuration of dactyloxene-B and -C Bruno Maurer, Arnold Hauser, Walter Thommen, Karl H. Schulte-Elte, G¨¹nther Ohloff Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 9-hydroxymenthol ÏàËÆ¶È:54.5% Phytochemistry 1991 30 3981-3987 Biotransformation of monoterpenoids, (− - and menthols, terpinolene and carvotanacetone by Aspergillus speciesYoshinori Asakawa, Hironobu Takahashi, Masao Toyota, Yoshiaki Noma Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (2S,3S,4R)-2-Azido-dodecane-1,3,4-triol C12H25N3O3 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2011 19 221-228 Synthesis of truncated analogues of the iNKT cell agonist,¦Á-galactosyl ceramide (KRN7000), and their biological evaluation Natacha Veerapen, Faye Reddington, Mariolina Salio, Vincenzo Cerundolo, Gurdyal S. Besra Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 8-hydroxy-1-menthol C10H18O ÏàËÆ¶È:54.5% Phytochemistry 1988 27 3861-3869 Preparation of biologically active substances and animal and microbial metabolites from menthols,cineoles and kauranes Yoshinori Asakawa,Reiko Matsuda,Motoo Tori,Toshihiro Hashimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound (E)-3(X=F) ÏàËÆ¶È:54.5% Organic letters 2000 2 831-834 Hyperconjugative Control by Remote Substituents of Diastereoselectivity in the Oxygenation of Hydrocarbons Mar¨ªa E. Gonz¨¢lez-Nuñez, Jorge Royo, Gloria Castellano, Cecilia Andreu, Carmen Boix, Rossella Mello, and Gregorio Asensio Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . tert-butyl rac-trans-2-(triisopropylsilyloxy)cyclohexylcarbamate C20H41NO3Si ÏàËÆ¶È:54.5% Heterocycles 2009 77 1123-1146 Synthesis of Annulated 1,4-Dioxanes and Perhydro-1,4-oxazines by Domino-Wacker-Carbonylation and Domino-Wacker-Mizoroki-Heck Reactions Lutz F. Tietze, Arne Heins, Mohammad Soleiman-Beigi, and Christian Raith Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (1R)-1-[(2R)-2-oxiranyl]-1-octanol ÏàËÆ¶È:54.5% Heterocycles 2004 62 857-868 Asymmetric Synthesis of Panaxydol and Its Stereoisomers Hsi-Jung Yu, Chang-Ming Sun, Chien-Chih Chen, Tsao-Chin Wu, Chia-Ling Wei, and Chien-Chang Shen* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . (1S)-1-[(2S)-2-oxiranyl]-1-octanol ÏàËÆ¶È:54.5% Heterocycles 2004 62 857-868 Asymmetric Synthesis of Panaxydol and Its Stereoisomers Hsi-Jung Yu, Chang-Ming Sun, Chien-Chih Chen, Tsao-Chin Wu, Chia-Ling Wei, and Chien-Chang Shen* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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- and menthols, terpinolene and carvotanacetone by Aspergillus species