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²éѯ½á¹û£º¹²²éµ½164¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . isomenthol ÏàËÆ¶È:58.3% Magnetic Resonance in Chemistry 2008 46 1188-1194 Enantiomeric differentiation of oxygenated p-menthane derivatives by 13C NMR using Yb(hfc)3 (pages 1188¨C1194) Don Antoine Lanfranchi, Marie-C¨¦cile Blanc, Muriel Vellutini, Pascale Bradesi, Joseph Casanova and F¨¦lix Tomi Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 12 ÏàËÆ¶È:58.3% Tetrahedron Letters 1994 35 3413-3416 Isolation and synthesis of siphonarienal a new polypropionate from Siphonaria grisea Manuel Norte, Jos¨¦ J. Fern¨¢ndez, Agust¨ªn Padilla Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2,4,6-trimethylnonan-1-ol C12H26O ÏàËÆ¶È:58.3% The Journal of Organic Chemistry 2005 70 1808-1827 Novel Cuticular Hydrocarbons from the Cane Beetle Antitrogus parvuluss4,6,8,10,16-Penta- and 4,6,8,10,16,18-HexamethyldocosanessUnprecedented anti-anti-anti-Stereochemistry in the 4,6,8,10-Methyltetrad Sharon Chow, Mary T. Fletcher, Lynette K. Lambert, Oliver P. Gallagher, Christopher J. Moore, Bronwen W. Cribb, Peter G. Allsopp, and William Kitching Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (2S,4S,6S)-2,4,6-trimethylnonan-1-ol ÏàËÆ¶È:58.3% Helvetica Chimica Acta 2013 96 1968-1977 Divergent Enantioselective Total Synthesis of Siphonarienal, Siphonarienone, and Pectinatone Jhillu Singh Yadav, D. Narasimha Chary, Nagendra Nath Yadav, Sandip Sengupta and Basi V. Subba Reddy Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (7S,8R,10R,Z)-7,8-dihydroxy-10-propyl-3,4,7,8,9,10-hexahydro-2H-oxecin-2-one C12H20O4 ÏàËÆ¶È:58.3% RSC Advances 2013 3 23343-23346 The first stereoselective total synthesis of the Z-isomer of (6S,7R,9R)-6,7-dihydroxy-9-propylnon-4-eno-9-lactone Palakodety Radha Krishna, Sunchu Prabhakar and Kallaganti V. S. Rama Krishna Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 57 ÏàËÆ¶È:58.3% Organic Magnetic Resonance 1975 7 426-432 13C-NMR-Spektren von Monoterpenen F. Bohlmann, R. Zeisberg and E. Klein Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 4¦Â-(pent-2-enylolactone)-hexatriacontane C41H78O2 ÏàËÆ¶È:58.3% Journal of Asian Natural Products Research 2012 14 7-13 Two new triterpenoids from Cichorium intybus L. roots Rajkumari Kumari, Mohammed Ali & Vidhu Aeri Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (2E,4E)-and (2Z,4E)-3-Methyl-5-(2,6,6-trimethylcyclohex-1-en-1-yl)penta-2,4-dienal ÏàËÆ¶È:58.3% Helvetica Chimica Acta 2013 96 259-265 Base-Induced Decarboxylation of Polyunsaturated ¦Á-Cyano Acids Derived from Malonic Acid: Synthesis of Sesquiterpene Nitriles and Aldehydes with ¦Â-, ¦Õ-, and ¦×-End Groups Laurent Dufoss¨¦, Dominique Cartier, Benoist Valla, Mireille Fouillaud, Roger Labia and Alain Valla Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (2'S)-2-(2'-Chloro-3'-methylbutanamido)-3-methylbenzoic acid C13H16ClNO3 ÏàËÆ¶È:58.3% Chirality 2013 25 865-870 Stereoselective Synthesis of (3R)-3-Alkyl-4,1-Benzoxazepine-2,5-Diones (pages 865¨C870) Bushra Nisar, Abdul Rauf Raza, David Stc. Black, Naresh Kumar and Muhammad Nawaz Tahir Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (1RS,2SR,3SR,4SR)-3-ethyl-2-methylbicyclo[2.2.2]oct-5-ene-2-carbaldehyde ÏàËÆ¶È:58.3% Chemistry & Biodiversity 2014 11 1470-1516 endo/exo Stereoselectivity in DielsAlder Reactions of ,¦Â-Dialkylated Conjugated Enals to Cyclic 1,3-Dienes: Intermediates in the Synthesis of (− -¦Â-Santalol and Its AnalogsChristian Chapuis, David Skuy, Jean-Yves de Saint Laumer and Robert Brauchli Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Compound 5 ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry Letters 1991 1 535-538 The enzymatic Baeyer-Villiger oxidation: synthesis of the C11¨CC16 subunit of ionomycin Michael J. Taschner, Quin-Zene Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 8-(tert-butyldiphenylsilyloxy)-(3S,7R)-3,7-dimethyl-1-octanol C26H40O2Si ÏàËÆ¶È:56.2% The Journal of Organic Chemistry 2013 78 5970-5986 Highly Stereocontrolled Total Synthesis of ¦Â-d-Mannosyl Phosphomycoketide: A Natural Product from Mycobacterium tuberculosis Nan-Sheng Li, Louise Scharf, Erin J. Adams, and Joseph A. Piccirilli Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Hedathiosulfonic acid A methyl thiosulfonate C13H26O2S2 ÏàËÆ¶È:53.8% Tetrahedron 2002 58 6405-6412 Hedathiosulfonic acids A and B, novel thiosulfonic acids from the deep-sea urchin Echinocardium cordatum Masaki Kita, Masami Watanabe, Noboru Takada, Kiyotake Suenaga, Kaoru Yamada, Daisuke Uemura Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 28 C16H23NO ÏàËÆ¶È:53.8% European Journal of Organic Chemistry 2011 794-801 Ring Expansion of 2-(1-Hydroxyalkyl)azetidines to 4-(2-Chloroethyl)oxazolidinones François Couty, Bruno Drouillat and Fr¨¦d¨¦ric Lem¨¦e Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (E)-2-(3-methylbuta-1,3-dienyl)-1,3,3-trimethylcyclohex-1-ene C14H22 ÏàËÆ¶È:53.8% European Journal of Organic Chemistry 2011 6713-6718 Copper(II)-Mediated Intramolecular Cyclization of (Z)-Chalcogenoenynes: Synthesis of 3-Halochalcogenophene Derivatives Daniela A. Barancelli, Ricardo F. Schumacher, Marlon R. Leite and Gilson Zeni Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (-)-(3R,4aS,4bS,7S,8aR,10aR)-3,7-dimethyl-9-oxo-1,4a,4b,7,8,8a,9,10a-octahydro-2,4,10-trioxaphenanthrene C13H18O4 ÏàËÆ¶È:53.8% European Journal of Organic Chemistry 2011 2789-2800 Synthesis of Naturally Occurring Cyclohexene Rings Using Stereodirected Intramolecular Diels¨CAlder Reactions Through Asymmetric 1,3-Dioxane Tethering Hajer Abdelkafi, Laurent Evanno, Alexandre Deville, Lionel Dubost, Ang¨¨le Chiaroni and Bastien Nay Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound C19H20OBr2Si ÏàËÆ¶È:53.8% Journal of the American Chemical Society 2004 126 14720-14721 Total Synthesis of Kendomycin: A Macro−C−Glycosidation Approach Yu Yuan, Hongbin Men, and Chulbom Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 79 C16H29NO3 ÏàËÆ¶È:53.8% Journal of Medicinal Chemistry 1992 35 4284-4296 Design and synthesis of novel FKBP inhibitors James R. Hauske, Peter Dorff, Susan Julin, Joseph DiBrino, Robin Spencer, Rebecca Williams Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 38 ÏàËÆ¶È:53.8% Organic Magnetic Resonance 1984 22 180-186 Conformations and 13C NMR shifts in tetralins Hans-jörg Schneider and Pawan Kumar Agrawal Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . cis-2-methyl-1,2,3,4-tetrahydronaphthalen-1-yl acetate ÏàËÆ¶È:53.8% Organic Magnetic Resonance 1984 22 180-186 Conformations and 13C NMR shifts in tetralins Hans-jörg Schneider and Pawan Kumar Agrawal Structure 13C NMR ̼Æ×Ä£Äâͼ |

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-¦Â-Santalol and Its Analogs