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1 . Lignoren C15H26O ÏàËÆ¶È:73.3% Journal of Basic Microbiology 2004 44 317-319 Lignoren, a new sesquiterpenoid metabolite from Trichoderma lignorum HKI 0257 Albrecht Berg, Hilaire V. Kemami Wangun, Augusin E. Nkengfack and Brigitte Schlegel Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Citrantifidiol C15H28O2 ÏàËÆ¶È:73.3% Journal of Agricultural and Food Chemistry 2008 56 3569-3573 Citrantifidiene and Citrantifidiol: Bioactive Metabolites Produced by Trichoderma citrinoviride with Potential Antifeedant Activity toward Aphids Antonio Evidente, Gaetano Ricciardiello, Anna Andolfi, Maria Agnese Sabatini, Sonia Ganassi, Claudio Altomare, Mara Favilla and Dominique Melck Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Viridenepoxydiol C15H28O3 ÏàËÆ¶È:73.3% Journal of Agricultural and Food Chemistry 2006 54 6588-6592 Viridenepoxydiol, a New Pentasubstituted Oxiranyldecene Produced by Trichoderma viride Antonio Evidente, Annalisa Cabras, Lucia Maddau, Francesco Marras, Anna Andolfi, Dominique Melck, and Andrea Motta Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . cyclonerodiol ÏàËÆ¶È:73.3% Journal of Agricultural and Food Chemistry 2000 48 4687-4692 Isolation and Characterization of Fungal Inhibitors from Epichloë festucae Qin Yue, Christina J. Miller, James F. White, Jr., and Michael D. Richardson Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . cyclonerodiol oxide C15H29O3 ÏàËÆ¶È:64.2% Chemical & Pharmaceutical Bulletin 1984 32 4419-4425 Fungal Metabolites. II. Structural Elucidation of Minor Metabolites, Valinotricin, Cyclonerodiol Oxide, and Epicyclonerodiol Oxide, from Trichoderma polysporum TETSURO FUJITA,YOSHIHISA TAKAISHI,YOSHIO TAKEDA,TETSUJI FUJIYAMA and TAKAHITO NISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (Z)-6,10-dimethyl-5,9-undecadien-2-ol C13H24O ÏàËÆ¶È:61.5% Phytochemistry 1995 40 1133-1137 Biotransformations of acyclic terpenoids, (¡À)-cis-nerolidol and nerylacetone, by plant pathogenic fungus, Glomerella cingulata Mitsuo Miyazawa, Hirokazu Nankai, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Neryl isopropanol ÏàËÆ¶È:61.5% Magnetic Resonance in Chemistry 2005 43 176-179 Enantiomeric differentiation of acyclic terpenes by 13C NMR spectroscopy using a chiral lanthanide shift reagent Marie-C¨¦cile Blanc, Pascale Bradesi and Joseph Casanova Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (-)-¦Ã-muurolene ÏàËÆ¶È:60% Phytochemistry 1987 26 2367-2370 New prenylated phenolics from Piper auritum Stephen A. Ampofo,Vassilios Roussis,David F. Wiemer Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (+)-¦Á-Bisabolol ÏàËÆ¶È:60% Phytochemistry 1980 19 461-462 Constituents of the essential oil of Salvia stenophylla C. Jequier, G. Nicollier, R. Tabacchi, J. Garnero Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 6-acetamido-1,1,1-trichloroundecane C13H24NOCl3 ÏàËÆ¶È:58.3% Journal of Natural Products 2001 64 572-577 Polychlorinated Acetamides from the Cyanobacterium Microcoleus lyngbyaceus Michael A. Orsini, Lewis K. Pannell, and Karen L. Erickson Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-(1'-Isopropenyl-2'2'-dimethylcyclopentyl)propanal C13H22O ÏàËÆ¶È:58.3% Helvetica Chimica Acta 1980 63 154-190 Photochemische Reaktionen. 106. Mitteilung. Zur Photochemie tetraalkylsubstituierter ¦Ã-Keto-olefine Jacob Berger, Michikazu Yoshioka, Markus P. Zink, Hans R. Wolf, Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 2 ÏàËÆ¶È:58.3% Tetrahedron Letters 2000 41 4587-4590 Facile synthesis of amino bicyclo[2.2.1]heptyl alcohol and its application for enantioselective additions of diethylzinc to aldehydes Naoto Hanyu, Takashi Mino, Masami Sakamoto, Tsutomu Fujita Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3,7,11-trimethyldodec-10-en-1-ol C15H30O ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry 2010 18 3116-3124 Structure¨Cactivity relationships in the conversion of vitamin K analogues into menaquinone-4. Substrates essential to the synthesis of menaquinone-4 in cultured human cell lines Yoshitomo Suhara, Akimori Wada, Yoji Tachibana, Masato Watanabe, Kanae Nakamura, Kimie Nakagawa, Toshio Okano Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2,3,4,5,6,7,8,9,10,11,12,13-Dodecahydro-2-[ (2H3)methyl]-1H-cyclopenta[12]annulene ÏàËÆ¶È:54.5% Helvetica Chimica Acta 2009 92 1782-1799 Synthesis of Deuterium-Labeled Perfume Ingredients as Internal Standards for Their GC/MS Quantification Christian Chapuis, Carole Cantatore, Peter Fankhauser, Ren¨¦ Challand, Jean-Jacques Riedhauser Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . trans-bicyclo[4.4.0]decan-2-one C10H16O ÏàËÆ¶È:54.5% Helvetica Chimica Acta 1981 64 2002-2021 3-Triethylsilyloxypentadienyllithium, a Versatile 1,3-Diene- or Vinyl Ketone-Building Block Wolfgang Oppolzer, Roger L. Snowden, Dana P. Simmons Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 5b ÏàËÆ¶È:54.5% Chinese Chemical Letters 2008 19 403-405 Synthesis of macrocyclic lactones with methoxysulfonyl side chain Chuan Jin Hou, Xiao Mei Liang, Jing Ping Wu, Dao Quan Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 2,2-Dideuterio-5.5,9-trimethyl-l-(trideuteriomethyl)spiro[3.5]nonan-l-ol ÏàËÆ¶È:54.5% Helvetica Chimica Acta 1980 63 154-190 Photochemische Reaktionen. 106. Mitteilung. Zur Photochemie tetraalkylsubstituierter ¦Ã-Keto-olefine Jacob Berger, Michikazu Yoshioka, Markus P. Zink, Hans R. Wolf, Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (4R*,5R*)-4,5-Methano-4,7-dimethyl-6-octen-2-on C11H18O ÏàËÆ¶È:54.5% Helvetica Chimica Acta 1980 63 571-587 Photochemische Reaktionen. 107. Mitteilung. Zur Photochemie offenkettiger 2,6-bzw. 2,7-Dien-Carbonylverbindungen Michikazu Yoshioka, Keitaro Ishii, Hans Richard Wolf Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . elijopyrone C C12H18O2 ÏàËÆ¶È:54.5% Natural Product Research 1995 6 303-308 Elijopyrones A-D: New ¦Á-pyrones from a Marine Actinomycete Steven G. Toske; Paul R. Jensen; Christopher A. Kauffman; William Fenical Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 3l C12H23NO2S2 ÏàËÆ¶È:54.5% Canadian Journal of Chemistry 2006 84 1515-1519 Synthesis of -hydroxy dithiocarbamate derivatives via regioselective addition of dithiocarbamate anion to epoxide in water Azim Ziyaei-Halimjani and Mohammad R. Saidi Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (2S)-2-Cyclohexyl-2-methyloxirane ÏàËÆ¶È:54.5% Molecules 2012 17 1617-1634 Enantioselective Synthesis of 2,2-Disubstituted Terminal Epoxides via Catalytic Asymmetric Corey-Chaykovsky Epoxidation of Ketones Toshihiko Sone,Akitake Yamaguchi,Shigeki Matsunaga and Masakatsu Shibasaki Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 1-Oxaspiro[2.13]hexadecane ÏàËÆ¶È:54.5% Helvetica Chimica Acta 2012 95 428-447 Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 1-cyclobutanecarbonyl-2-oxo-3-pyrrolidinecarbonitrile C10H12N2O2 ÏàËÆ¶È:54.5% Journal of Heterocyclic Chemistry 2005 42 543-549 Synthesis of 1-acyl-2-oxo-3-pyrrolidinecarbonitriles by the reaction of 2-acylamino-4,5-dihydro-3-furancarbonitriles with sodium iodide Kenji Yamagata,Fumi Okabe,Hiroshi Maruoka and Yoshinobu Tagawa Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . ethyl 1,2,2-trimethylcyclopentane-1-carboxylate ÏàËÆ¶È:54.5% Indian Journal of Chemistry 2006 45B 2465-2468 An efficient ring-closing metathesis reaction based approach to 1,2,2-trimethylcyclo-pentanemethanol. Formal synthesis of (¡À)‑herbertene and (¡À)‑cuparenes Srikrishna,A; Satyanarayana,G Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . spiro[cyclopentane-1,17'-[(3,14)]-diazatricyclo[12.3.1.1(3,16)]nonadecane]-2',15',18',19'-tetraone C21H30N2O4 ÏàËÆ¶È:54.5% Heterocycles 2007 71 2331-2345 Synthesis of New Tricyclic Spirobispidines via Ring Closing Metathesis Reaction Christian Hametner, Daniel Dangl, Kurt Mereiter, Martina Marchetti, and Johannes Fröhlich Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . Compound 11 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry Letters 2005 15 2331-2334 N-Hydroxy sulfonimidamides as new nitroxyl (HNO) donors Richard L. Pennington, Xin Sha, S. Bruce King Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . (1S,8aR)-1-Aminomethyl indolizidine C9H18N2 ÏàËÆ¶È:54.5% Tetrahedron Letters 2001 42 7003-7005 A short synthesis of (1S,8aR)-1-aminomethyl indolizidine. The heterocyclic core of stelletamides Ronaldo A Pilli, Paulo R Zanotto, Maria Alice Böckelmann Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . compound 2 C11H17ClO2 ÏàËÆ¶È:54.5% Tetrahedron Letters 2002 43 837-841 Intramolecular TiCl4-mediated cyclization reaction of ¦Â-hydroxy alkynyl acetals Yong-Hyun Kim, Kee-Young Lee, Chang-Young Oh, Jae-Gwon Yang, Won-Hun Ham Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 3-(S)3,7-Dimethyl-2-oxo-oct-6-ene-1,3-diol ÏàËÆ¶È:54.5% Tetrahedron Letters 2002 43 2641-2643 (S)-3,7-Dimethyl-2-oxo-6-octene-1,3-diol: an aggregation pheromone of the Colorado potato beetle, Leptinotarsa decemlineata (Say) James E Oliver, Joseph C Dickens, Thomas E Glass Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 1-methylcycloundecanecarbonitrile ÏàËÆ¶È:54.5% Tetrahedron Letters 2004 45 7887-7889 Thermodecarbonylation of ¦Á-substituted cycloalkanones: a convenient one-carbon ring contraction method Georg R¨¹edi, Matthias A. Oberli, Hans-J¨¹rgen Hansen Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . compound 19 ÏàËÆ¶È:54.5% Tetrahedron Letters 2005 46 1867-1871 Approaches to installing a N-gem-dimethylmethylene-2-oxazolyl group and application to the synthesis of a second generation HIV protease inhibitor Norihiro Ikemoto, Ross A. Miller, Fred J. Fleitz, Jinchu Liu, Daniel E. Petrillo, Joseph F. Leone, Joseph Laquidara, Benjamin Marcune, Sandor Karady, Joseph D. Armstrong III, Ralph P. Volante Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 4-Isopropenyl-1-methyl-2-pyrrolidin-1-yl-cyclohexylamine ÏàËÆ¶È:54.5% Tetrahedron Letters 2005 46 6907-6910 Regio- and diastereoselective synthesis of bifunctionalized limonenes Michael V. Voronkov, Ramanaiah C. Kanamarlapudi, Paul Richardson Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . compound 7 ÏàËÆ¶È:54.5% Archiv der Pharmazie 1998 331 279-282 Effective Stereoselective Total Synthesis of 16,16-Dimethyl Prostaglandin E2 Ana Rodr¨ªguez, Miguel Nomen, Bernd W. Spur and Jean-Jacques Godfroid Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . compound 8 ÏàËÆ¶È:54.5% Archiv der Pharmazie 1998 331 279-282 Effective Stereoselective Total Synthesis of 16,16-Dimethyl Prostaglandin E2 Ana Rodr¨ªguez, Miguel Nomen, Bernd W. Spur and Jean-Jacques Godfroid Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 6-(tert-Butyldimethylsilyloxy)heptanal C13H28O2Si ÏàËÆ¶È:54.5% Organic & Biomolecular Chemistry 2007 5 1167-1169 Efficient synthesis of brussalexin A, a remarkable phytoalexin from Brussels sprouts M. Soledade C. Pedras, Qing-An Zheng and Mohammed G. Sarwar Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . N,N-Bis(5-cyanopentyl)butylamine C16H29N3 ÏàËÆ¶È:54.5% Journal of the Chemical Society, Perkin Transactions 1 1997 3197-3204 Regioselective biotransformations of dinitriles using Rhodococcus sp. AJ2701 Otto Meth-Cohn and Mei-Xiang Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . S-ethyl(R)-3-(tert-butyldimethylsiloxy)butanoate C8H16O2SSi ÏàËÆ¶È:54.5% Heterocycles 2000 52 1105-1123 Stereoselective Total Synthesis of Cephalosporolide D Isamu Shiina,* Hidehiko Fujisawa, Toshihiro Ishii, and Yoshio Fukuda Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . cyclo-[L-Leucyl-L-isoleucyl]2 C24H44N4O4 ÏàËÆ¶È:54.5% Tetrahedron 2008 64 3147-3152 Cyclic tetrapeptides from marine bacteria associated with the seaweed Diginea sp. and the sponge Halisarca ectofibrosa Wimolpun Rungprom, Eric R.O. Siwu, Lynette K. Lambert, Chutiwan Dechsakulwatana, Michael C. Barden, Udom Kokpol, Joanne T. Blanchfield, Masaki Kita, Mary J. Garson Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . (1R,2R,3S,6S)-3-isopropyl-6-methylcyclohexane-1,2-diol C10H20O2 ÏàËÆ¶È:54.5% Russian Journal of Organic Chemistry 2010 46 1786-1789 Hydrogenation and conformational analysis of (1R,2R,6S)-3-methyl-6-(1-methylethenyl)cyclohex-3-ene-1,2-diol O. V. Ardashov, A. M. Genaev, I. V. Il¡¯ina, D. V. Korchagina and K. P. Volcho, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . cis-8-acetamido-o-menthone ÏàËÆ¶È:54.5% Russian Journal of Organic Chemistry 2006 42 1141-1145 Verbanone in the synthesis of amidoketones from o-menthane series S. S. Koval¡¯skaya, N. G. Kozlov and A. V. Tkachev Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . compound X C11H20O ÏàËÆ¶È:54.5% Russian Journal of Organic Chemistry 2002 38 810-822 Acid-catalyzed Reactions of Camphene and ¦Á-Fenchene Epoxides O. I. Yarovaya, D. V. Korchagina, Yu. V. Gatilov and V. A. Barkhash Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . nitropeptin C11H18N3O7Na ÏàËÆ¶È:54.5% The Journal of Antibiotics 1987 40 709-713 NITROPEPTIN, A NEW DIPEPTIDE ANTIBIOTIC POSSESSING A NITRO GROUP KAZUNORI OHBA, HIROSHI NAKAYAMA, KAZUO FURIHATA, AKIRA SHIMAZU, TOYOSIGE ENDO, HARUO SETO, NOBORU OTAKE Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . 1-cyclohexyl-2-methyl-2-nitropropan-1-ol ÏàËÆ¶È:54.5% 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 44 . 3-butyl-3-methyl-1,6-hexanediol ÏàËÆ¶È:54.5% European Journal of Organic Chemistry 2010 6372-6384 (R)-(+)-[VCD(¨C)984]-4-Ethyl-4-methyloctane: A Cryptochiral Hydrocarbon with a Quaternary Chiral Center. (1) Synthesis of the Enantiopure Compound and Unambiguous Determination of Absolute Configuration Takuma Fujita, Kazuhiro Obata, Shunsuke Kuwahara, Atsufumi Nakahashi, Kenji Monde, John Decatur and Nobuyuki Harada Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . (R)-7-hydroxy-9-methyldecan-5-one C11H22O2 ÏàËÆ¶È:54.5% European Journal of Organic Chemistry 2010 4785-4801 Conversion of Conjugated Enones into Enantiomerically Pure -Hydroxy Ketones or 1,3-Diols ¨C Samarium(II) Bromide Reductions of Protected ,-Dihydroxy Ketones Andreas Zörb and Reinhard Br¨¹ckner Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . (4S,8S)-8,9-epoxy-p-menth-1-en-7-ol C10H16O2 ÏàËÆ¶È:54.5% Australian Journal of Chemistry 1996 49 741-749 7,9-Dihydroxy-1,8-cineole and 2¦Á,7-Dihydroxy-1,8-cineole: Two New Possum Urinary Metabolites RM Carman and AC Garner Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . 4,4-dimethyl-5-(2-methylprop-1-en-1-yl)oxolan-2(3H)-one C10H16O2 ÏàËÆ¶È:54.5% Helvetica Chimica Acta 2012 95 2123-2167 Syntheses of Racemic and Scalemic cis-Chrysanthemic Acid from ¦Â,-Unsaturated Cyclohexanol Alain Krief, St¨¦phane Jeanmart, Humaira Y. Gondal and Adrian Kremer Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . compound 11a C11H19NO2 ÏàËÆ¶È:54.5% Canadian Journal of Chemistry 1996 74 2434-2443 A revised structure for the piperidine alkaloid andrachamine Sibel Mill, Claude Hootel¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 1-pyrrolidin-1-yl hexan-1-thione C10H19NS ÏàËÆ¶È:54.5% Canadian Journal of Chemistry 2004 82 1289-1293 A new efficient synthesis of ¦Á-methyl-¦Â-ketoesters through an Eschenmoser sulfide reaction Christian Bellec, Olivier Gaurat Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . compound 15 ÏàËÆ¶È:54.5% 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 51 . ¦Â-Fenchol ÏàËÆ¶È:54.5% 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 52 . 4-tert-Butyl-1-butylcyclohexanol ÏàËÆ¶È:54.5% Tetrahedron 2012 68 7414-7421 Amberlyst®-15: a reusable heterogeneous catalyst for the dehydration of tertiary alcohols Lu¨ªs M.T. Frija, Carlos A.M. Afonso Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . 7¦Â-acetoxyhopan-22-ol ÏàËÆ¶È:54.5% Australian Journal of Chemistry 1989 42 243-257 A One- and Two-Dimensional 13C and 1H N.M.R. Study of Some Triterpenes of the Hopane, Stictane and Flavicene Groups AL Wilkins, J Bremer, J Ralph, PT Holland, KJ Ronaldson, PM Jager and PW Bird Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . 1,5,5,9-Tetramethylspiro[3.5]nonan-l-ol C13H24O ÏàËÆ¶È:53.8% Helvetica Chimica Acta 1980 63 154-190 Photochemische Reaktionen. 106. Mitteilung. Zur Photochemie tetraalkylsubstituierter ¦Ã-Keto-olefine Jacob Berger, Michikazu Yoshioka, Markus P. Zink, Hans R. Wolf, Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . 2,6-¶þ¼×»ù-2-»·ÒÑÏ©ÂÝ-(2',3'-ÑǼ׻ù-3'-ÒÒõ£»ù)»·¶¡Íé C14H20O ÏàËÆ¶È:53.8% Chemical Journal of Chinese Universities 2004 25 1051-1055 Improvement of Total Synthesis of (¡À)-Hinesol and (¡À)-Agarospirol WANG Jin-Jun,MORIA kiro, HATSUI Toshihide, TAKESHITA Hitoshi Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . N-[(R)-2-((N-Formyl-N-hydroxy)aminomethyl)-4-methylpent-anoyl]-D-alanine C23H43N3O5 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry Letters 2003 13 3161-3166 Reversed hydroxamate-Bearing thermolysin inhibitors mimic a high-energy intermediate along the enzyme-Catalyzed proteolytic reaction pathway Jung Dae Park, Dong H. Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . Geranyl isopropanol ÏàËÆ¶È:53.8% Magnetic Resonance in Chemistry 2005 43 176-179 Enantiomeric differentiation of acyclic terpenes by 13C NMR spectroscopy using a chiral lanthanide shift reagent Marie-C¨¦cile Blanc, Pascale Bradesi and Joseph Casanova Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . compound C23H33N5O8S2 ÏàËÆ¶È:53.8% Zeitschrift f¨¹r Naturforschung B 2004 59 1415-1422 N-Benzyl and N-Heptyl Substituted Tetraazacyclodecanes (In German) H. Schumann, K. Kuse, and S. Dechert Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . compound ii ÏàËÆ¶È:53.8% Journal of the American Chemical Society 2010 132 5300-5308 Biomimetic Syntheses from Squalene-Like Precursors: Synthesis of ent-Abudinol B and Reassessment of the Structure of Muzitone Matthew A. Boone, Rongbiao Tong, Frank E. McDonald, Sheri Lense, Rui Cao and Kenneth I. Hardcastle Structure 13C NMR ̼Æ×Ä£Äâͼ |
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