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²éѯ½á¹û£º¹²²éµ½15¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . hamavellone B C11H16O2 ÏàËÆ¶È:63.6% Tetrahedron 2008 64 11028-11033 Novel cyclopropyl diketones and 14-membered macrolides from the soil fungus Hamigera avellanea BCC 17816 Masahiko Isaka, Panida Chinthanom, Sukitaya Veeranondha, Sumalee Supothina, J. Jennifer Luangsa-ard Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (1R,3S)-(3)-3-(2-bromoethyl)-2,2-dimethyl-1-[(E)-3-oxobutenyl]cyclopropane C11H17BrO ÏàËÆ¶È:63.6% Russian Journal of Organic Chemistry 2003 39 75-81 Approaches to Epothilone Carboanalogs Starting from ¦¤3-Carene F. A. Akbutina, I. F. Sadretdinov, O. M. Kuznetsov, E. V. Vasil'eva and M. S. Miftakhov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 5-cyclohexyl-5-oxopentanoic acid ÏàËÆ¶È:54.5% Phytochemistry 2002 61 669-673 Oxidative cleavage of the C¨CC bond of 3,6-dialkylcyclohexane-1,2-diones by cell suspension cultures of Marchantia polymorpha Yoshitomo Matsuura, Wen Chai, Etsuko Endoh, Jyumpei Suhara, Hiroki Hamada,C. Akira Horiuchi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 3 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 -------------------------------------------------------------------------------- 5 . (5R)-5-(3-bromopropen-2-yl)-2,3,4,4-tetramethylcyclohex-2-enone ÏàËÆ¶È:53.8% Indian Journal of Chemistry 2008 47B 449-459 Enantiospecific synthesis of thaps-8-en-5-ol via stereospecific Srikrishna,A; Anebouselvy,K Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 9-(4-Chlorophenyl)-3,3,6,6-tetramethyl-3,4,6,7-tetrahydroacridine-1,8(2H,5H,9H,10H)-dione C23H26ClNO2 ÏàËÆ¶È:50% Molecules 2009 14 1468-1474 An Efficient One-Pot Three-Component Synthesis of Fused 1, 4-Dihydropyridines Using HY-Zeolit Mohammad Nikpassand, Manouchehr Mamaghani and Khalil Tabatabaeian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Xestoaminol A C14H29NO ÏàËÆ¶È:50% Journal of Natural Products 1990 Vol 53 978 Novel Marine Sponge Amino Acids, 10. Xestoaminoh from Xestaspongia sp. Carlos Jim¨¦nez, Phillip Crews Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 7-aza-3,3,4-trimethyl-2-thiatricyclo[5.4.0.01,4]undecane-8-thione C12H19NS2 ÏàËÆ¶È:50% Heterocycles 2000 53 2781-2788 Photochemistry of N-3-Butenyl- and N-4-Pentenylglutarimides: Intramolecular Thietane Formation and the Fission of Thietane Ring Kazuaki Oda,* Takeshi Ishioka, Yuichi Fukuzawa, Naozumi Nishizono, and Minoru Machida* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (1R,7aS)-7a-methoxyethyl-1,4-dimethyl-5,6,7,7a-tetrahydrindan-5-one C14H22O2 ÏàËÆ¶È:50% Tetrahedron 1990 46 761-774 Stereocontrolled synthesis of (-)-prezizanol,(-)-prezizaene, their epimers and (-)-allokhusiol Kazutoshi Sakurai, Takeshi Kitahara, Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3,3,6,6-tetramethyl-9-phenyl-3,4,6,7,9,10-hexahydro-(2H,5H)-acridine-1,8-dione C23H27NO2 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2011 48 69-73 Eco-friendly and facile one-pot multicomponent synthesis of acridinediones in water under microwave Satish Kumar Singh and Krishna Nand Singh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . papyracon B C14H20O5 ÏàËÆ¶È:50% The Journal of Antibiotics 1995 48 154-157 New Metabolites with Nematicidal and Antimicrobial Activities from the Ascomycete Lachhum papyraceum (Karst.) Karst VI. Structure Determination of Non-halogenated Metabolites Structurally Related to Mycorrhizin A MARC STADLER, HEIDRUN ANKE, RUDONG SHAN, OLOV STERNER Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (-)-isothujyl acetate ÏàËÆ¶È:50% Organic Magnetic Resonance 1974 6 184-189 The NMR spectra and conformations of cyclic compounds: IX¡ªconformational studies of bicyclo(3,1,0)hexane derivatives by 13C NMR Raymond J. Abraham, Collette M. Holden, Philip Loftus and David Whittaker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 5-Methyl-2-dihexylamino-2-cyclopenten-1-one C18H33ON ÏàËÆ¶È:50% Journal of Agricultural and Food Chemistry 2001 49 5383-5390 Systematic Studies on Structure and Physiological Activity of Cyclic ¦Á-Keto Enamines, a Novel Class of ¡°Cooling¡± Compounds Harald Ottinger, Tomislav Soldo, and Thomas Hofmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 1-methyl-alkylatcd bicyclo[2.2.2]octan-2-ol C12H22O ÏàËÆ¶È:50% Flavour and Fragrance Journal 1993 8 297-306 Structure¨Codour correlation. Part XVIII.1 Partial structures of patchoulol with bicyclo[2.2.2]octane skeleton Peter Weyerstahl, Christian Gansau and Helga Marschall Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (1R*,5S*,2'Z)-5-Methyl-1-(-20-pentenyl)bicyclo[3.1.0]hexan-2-one C13H21N3O ÏàËÆ¶È:50% Flavour and Fragrance Journal 2001 16 175-179 Syntheses and odour descriptions of jasmine lactone and cis-jasmone analogues bearing cyclopropane moieties Hiromasa Kiyota, Emi Higashi, Takanori Koike and Takayuki Oritani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- Copyright © 2009-2011 ÉϺ£Î¢Æ×ÐÅÏ¢¼¼ÊõÓÐÏÞ¹«Ë¾ Shanghai Micronmr Infor Technology Co., Ltd., All Rights Reserved µØÖ·£ºÉϺ£ÊÐÑîÆÖÇøºªµ¦Â·100ºÅ61¶°131ÊÒ(¸´µ©¿Æ¼¼Ô°), Óʱà:200437 E-mail: micronmr@126.com ×Éѯµç»°:086-021-61736083 »¦ICP±¸10026489ºÅ |
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