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²éѯ½á¹û£º¹²²éµ½205¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . methyl (2S)-2-{[(tert-butyloxy)carbonyl]amino}-3-(4-hydroxyphenyl)propanoate C18H17NO3 ÏàËÆ¶È:70% Helvetica Chimica Acta 2013 96 1564-1570 Total Synthesis of a Pyrrolidin-2-one with the Structure Proposed for the Alkaloid Rigidiusculamide A Palakodety Radha Krishna and Bonepally Karunakar Reddy Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . nonyl 4-hydroxybenzoate C16H24O3 ÏàËÆ¶È:63.6% Helvetica Chimica Acta 2003 Vol. 86 2021 New Glycosides from Salvia moorcroftiana (Lamiaceae) Muhammad Zahid, Muhammad Saeed, Muhammad Asim, Omar Ishrud, Shihua Wu,Viqar Uddin Ahmad, and Yuanjiang Pan Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-trifluoroacetylamino-3-carboxy-4-phenylbutyric acid ÏàËÆ¶È:63.6% Heterocycles 2002 57 501-513 Amino Acid-derived 4-Alkyl-4-carboxy-2-azetidinones. New Insights into ¦Â-Lactam Ring Formation and N-Deprotection Guillermo Gerona-Navarro, Ma Angeles Bonache, Nuria Reyero, Ma Teresa Garc¨ªa-L¨®pez, and Rosario Gonz¨¢lez-Muñiz* Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Boc-Tyr-CO2Me C15H21NO5 ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 2012 20 5139-5149 Synthesis and biological evaluation of tyrosine modified analogues of the ¦Á4¦Â7 integrin inhibitor biotin-R8ERY Stefanie Papst, Anaïs F.M. Noisier, Margaret A. Brimble, Yi Yang, Geoffrey W. Krissansen Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 4-hydroxyphenethyl methyl succinate C13H16O5 ÏàËÆ¶È:61.5% Journal of Asian Natural Products Research 2009 11 912-917 Two new compounds from the broth of the marine fungus Penicillium griseofulvum Y19-07 Ya-Nan Wanga, Li Tianbc, Hui-Ming Huaa, Xuan Lua, Sha Suna, Hong-Hua Wua and Yue-Hu Peia Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . tyrosol ÏàËÆ¶È:60% Natural Product Research 2004 18 29-32 Phenolic components of Olea Europaea ¨C isolation of tyrosol derivatives Armandodoriano Bianco; Cristiana Melchioni; Alessia Ramunno; Giovanni Romeo; Nicola Uccella Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2-(4-hydroxyphenyl)ethanol ÏàËÆ¶È:60% Korean Journal of Pharmacognosy 2004 35(1) 80-87 The Chemical Structures and Their Antioxidant Activity of the Components Isolated from the Heartwood of Hemiptelea davidii Chang, Bok-Sim; Kwon, Yong-Soo; Kim, Chang-Min Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . tyrosol(ÀÒ´¼) ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2011 42(5) 848-851 Polyphenols from leaves of Olea europaea WANG Xiao-fei, LI Chen ,ZHENG Yuan-yuan,DI Duo-long Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Tyrosol C9H13NO2 ÏàËÆ¶È:60% Archives of Pharmacal Research 2011 Vol 34, No 8 1289-1296 Phenolic Constituents of Acorus gramineus Cheol Hyeong Park, Ki Hyun Kim, Il Kyun Lee, Seung Young Lee, Sang Un Choi, Jei Hyun Lee, and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2-(4-Hydroxyphenyl)ethanol ÏàËÆ¶È:60% Archives of Pharmacal Research 2009 32 1681-1687 Cytotoxic phenolic compounds from Chionanthus retusus Jong Hwan Kwak, Min Woo Kang, Jong Hwa Roh, Sang Un Choi and Ok Pyo Zee Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 15 C11H22NO6 ÏàËÆ¶È:60% Tetrahedron Letters 2001 42 5709-5711 Diastereospecific formal synthesis of (2R,3S)-2-amino-tetradeca-5,7-dien-3-ol isolated from Xestospongia sp. Nicole Langlois Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . tyrosol ÏàËÆ¶È:60% Journal of Shenyang Pharmaceutical University 2011 28 120-123 Isolation and identification of chemical constituents from pine pollen TANG Yu, ZHANG Yu, YUAN Jiu-zhi, MA Yue-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound ÏàËÆ¶È:60% Tetrahedron 1999 55 6871-6882 Oscillapeptins A to F, serine protease inhibitors from the three strains of Oscillatoria agardhii Yusai Itou, Keishi Ishida, Hee Jae Shin, Masahiro Murakami Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (S)-2-[(4-hydroxybenzylidene)amino]-3-phenylpropi-onic acid methyl ester ÏàËÆ¶È:60% Journal of Medicinal Chemistry 2002 45 2410-2416 Inhibition of MIF Bioactivity by Rational Design of Pharmacological Inhibitors of MIF Tautomerase Activity Angeles Dios, Robert A. Mitchell, Bayan Aljabari, Jodi Lubetsky, KerryAnn O'Connor, Hong Liao, Peter D. Senter, Kirk R. Manogue, Elias Lolis, Christine Metz, Richard Bucala, David J. E. Callaway, and Yousef Al-Abed Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . tyrosol ÏàËÆ¶È:60% Qu¨ªmica Nova 2013 36 1004-1007 PHYTOTOXIC EFFECTS OF METABOLITES FROM Alternaria euphorbiicola AGAINST ITS HOST PLANT Euphorbia heterophylla Eduardo Vin¨ªcius Vieira Varejão* and Antônio Jacinto Demuner,Luiz Cl¨¢udio de Almeida Barbosa,Robert Weingart Barreto Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 23 C24H30N4O6S2 ÏàËÆ¶È:60% Chemistry-A European Journal 2001 7 4280-4295 Combinatorial Synthesis through Disulfide Exchange: Discovery of Potent Psammaplin A Type Antibacterial Agents Active against Methicillin-Resistant Staphylococcus aureus (MRSA) K. C. Nicolaou, Robert Hughes, Jeffrey A. Pfefferkorn, Sofia Barluenga and A. J. Roecker Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 1-Oxa-4-azacyclododec-8-ene-5,12-dione C10H16NO3 ÏàËÆ¶È:60% Tetrahedron 2012 68 5081-5086 The synthesis of 12-membered macrocycles containing a C1¨CC8 alkene unit via ring-closing metathesis Franc Požgan, Bogdan Štefane, Davor Kiđemet, Janez Smodiš, Rok Zupet Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . N-(2-(Nacetylacrylamido)ethyl)-2-chlorobutanamide C11H17ClN2O3 ÏàËÆ¶È:60% Tetrahedron 2012 68 5863-5881 CuCl-catalyzed radical cyclisation of N-¦Á-perchloroacyl-ketene-N,S-acetals: a new way to prepare disubstituted maleic anhydrides Andrea Cornia, Fulvia Felluga, Vincenzo Frenna, Franco Ghelfi, Andrew F. Parsons, Mariella Pattarozzi, Fabrizio Roncaglia, Domenico Spinelli Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . p-hydroxylbenzyl ethanol C8H10O2 ÏàËÆ¶È:60% Journal of Peking University (Health Sciences) 2004 36 12-17 Chemical constituents from chinese marine sponge Cinachyrella australiensis LI Li ya; DENG Zhi wei; LI Jun; FU Hong zheng; LIN Wen han Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (S)-tert-Butyl (6-hydroxyhex-1-en-3-yl)-carbamate C11H21NO3 ÏàËÆ¶È:60% The Journal of Organic Chemistry 2012 77 8828-8834 ¦Ã-Amino Alcohols via Organocascade Reactions Involving Dienamine Catalysis Chandrakumar Appayee, Americo J. Fraboni, and Stacey E. Brenner-Moyer Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 4-(2-hydroxyethyl) phenol ÏàËÆ¶È:60% China Journal of Chinese Materia Medica 2013 38 1172-1182 Chemical consitituents from root of Isatis indigotica WANG Xiao-liang, CHEN Ming-hua, WANG Fang, BU Peng-bin, LIN Sheng, ZHU Cheng-gen, LI Yu-huan, JIANG Jian-dong, SHI Jian-gong Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . tyrosol ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2013 44 1881-1886 Secondary metabolites of Eurotium cristatum from Fu Brick Tea and their biological activities PENG Xiao-yun, LIANG Fa-liang, LI Dong-li, CHEN Yu-chan, TAO Mei-hua, ZHANG Wei-min, ZHAO Yun-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Methyl 4-oxo-4-(phenylthio)butanoate ÏàËÆ¶È:60% Tetrahedron 2014 70 3259-3265 Pd-catalyzed Fukuyama cross-coupling of secondary organozinc reagents for the direct synthesis of unsymmetrical ketones Alan H. Cherney, Sarah E. Reisman Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 3-(4-hydroxyphenyl)propionyl choline C14H21NO3 ÏàËÆ¶È:58.3% Phytochemistry 2005 66 481-485 Tyrosine kinase inhibitors from the rainforest tree Polyscias murrayi Malcolm S. Buchanan, Anthony R. Carroll, Annette Edser, John Parisot,Rama Addepalli, Ronald J. Quinn Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . methyl 3-(2-oxo-2H-benzo[1,4]oxazin-3-yl)propanoate C12H11NO4 ÏàËÆ¶È:58.3% Journal of Heterocyclic Chemistry 2013 50 413-416 Novel 3-(2-Oxo-2H-benzo[1,4]oxazin-3-yl)propanoates from Dimethyl-2-oxoglutarate and Test of Their Biological Activity Kamel Hachama, Mohamed Khodja, Saad Moulay, Hocine Boutoumi, Lothar Hennig and Dieter Sicker Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . N-[2-(4-Hydroxyphenyl)ethyl]-2-hydroxy-3-methylpentanamide C14H21NO3 ÏàËÆ¶È:54.5% Journal of Natural Products 2010 73 313-316 Caste-Specific Tyramides from Myrmicine Ants Tappey. H. Jones, H. Martin Garraffo, Thomas F. Spande, Nirina R. Andriamaharavo, Jeffrey S. T. Gorman, Alexander J. Snyder, Andrew W. Jeter, Juan A. Torres, Roy R. Snelling and John W. Daly Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . Methyl 2-(4-phenoxyphenyl)acetate C15H14O3 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2011 19 4985-4999 N-Substituted homopiperazine barbiturates as gelatinase inhibitors Jun Wang, Carlos Medina, Marek W. Radomski, John F. Gilmer Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . Methyl N-amino-N-benzyl-(S)-valinate ÏàËÆ¶È:54.5% Tetrahedron Letters 2002 43 2873-2875 A facile stereospecific synthesis of ¦Á-hydrazino esters Umut Oguz, Garett G. Guilbeau, Mark L. McLaughlin Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . Methyl N-amino-N-benzyl-(S)-methioninate ÏàËÆ¶È:54.5% Tetrahedron Letters 2002 43 2873-2875 A facile stereospecific synthesis of ¦Á-hydrazino esters Umut Oguz, Garett G. Guilbeau, Mark L. McLaughlin Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . compound 4i C16H20ClN3O4 ÏàËÆ¶È:54.5% Tetrahedron Letters 2003 44 7475-7477 A versatile method for the synthesis of substituted 1-aminohydantoin derivatives Iv¨¢n B¨¦lai Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . compound 4 ÏàËÆ¶È:54.5% Tetrahedron Letters 2004 45 6603-6605 Two successive one-pot reactions leading to the expeditious synthesis of (-)-centrolobine Lucie Boulard, Samir BouzBouz, Janine Cossy, Xavier Franck, Bruno Figad¨¨re Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . compound 13 C14H16N2O2 ÏàËÆ¶È:54.5% Heterocycles 2001 55 2273-2278 Mono and Sequential Bis Solid Phase Alkylations of a (R)-Phenylglycinol Derived Pyrrolidinone Scaffold Armand Blommaert, Philippe James, Fanny Valleix, Henri-Philippe Husson, and Jacques Royer Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . 4-oxo-4-phenylacetylaminobutyric acid methyl ester C13H15NO4 ÏàËÆ¶È:54.5% The Journal of Antibiotics 2003 56 296-305 Synthesis and Structure-activity Relationship of Antifungal Coniothyriomycin Analogues KARSTEN KROHN,BRIGITTA ELSÄSSER,S¨¢NDOR ANTUS,KRISZTINA K¨®NYA and EBERHARD AMMERMANN Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . methyl 1-(4-hydroxybenzyl)-5-oxo-L-prolinate C13H15NO4 ÏàËÆ¶È:54.5% Molecules 2013 18 50-73 Synthesis of New Optically Active 2-Pyrrolidinones Panagiota Moutevelis-Minakakis, Eleni Papavassilopoulou and Thomas Mavromoustakos Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . compound 4 ÏàËÆ¶È:54.5% Australian Journal of Chemistry 1980 33 447-450 Carbon-13 N.M.R. spectra of 4-hydroxytetrahydroisoquinolinium chlorides GV Baddeley, SN Quessy and LR Williams Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . Methyl (3R,5S)-3-(4-Hydroxybenzyl)-5-methoxyisoxazolidine-5-carboxylate C13H17NO5 ÏàËÆ¶È:54.5% Helvetica Chimica Acta 2012 95 2481-2501 Synthesis of Enantiomerically Pure Isoxazolidine Monomers for the Preparation of ¦Â3-Oligopeptides by Iterative -Keto AcidHydroxylamine (KAHA) Ligations Ying-Ling Chiang, Justin A. Russak, Nancy Carrillo and Jeffrey W. Bode Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . (S)-2-Êå¶¡ÑõôÊ»ù°±»ù-3-±½¼×õ£Ñõ»ù-1-±û´¼ C15H21NO5 ÏàËÆ¶È:54.5% Chinese Journal of Organic Chemistry 2013 33 1939-1944 Synthesis of Right Segment of Ingramycin Gao Kaige, Sun Moran, Zhu Ming, Zhou Hang, Cao Qiwei, Yang Hua Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . methyl (¡À)-(2R,3R)-2-tert-butyl-1,2,3,4-tetrahydro-quinoline-3-carboxylate C15H21NO2 ÏàËÆ¶È:53.8% Journal of Heterocyclic Chemistry 2007 44 1059-1064 (¡À)-2-alkyl-1,2,3,4-tetrahydroquinoline-3-carboxylic esters by a catalyst and pressure dependent tandem reduction-reductive amination reaction Richard A. Bunce,Takahiro Nago and Nathan Sonobe Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . mixture of (1S,2R)-[1-benzyl-2-(1-tert-butyl-1H-tetrazole-5-yl)-2-hydroxyethyl]carbamic acid tert-butyl ester and (1S,2S)-[1-benzyl-2-(1-tert-butyl-1H-tetrazole-5-yl)-2-hydroxyethyl]carbamic acid tert-butyl ester 19H29N5O3 ÏàËÆ¶È:53.8% Heterocycles 2007 74 661-671 Zinc Iodide as an Efficient Catalyst in the TMS-Azide Modified Passerini Reaction Eva S. Schremmer and Klaus T. Wanner Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . Benzyl N-Boc-¦Ä-hydroxy-L-¦Á-aminovalerate ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry Letters 1999 9 3119-3122 Convenient synthesis of L-proline benzyl ester Armando C¨®rdova, Neal N. Reed, Jon A. Ashley, Kim D. Janda Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . methyl 3-(4-acetophenyl)-2-(tert-butoxycarbonylamino)propionate ÏàËÆ¶È:53.8% Tetrahedron Letters 2003 44 8931-8934 Catalytic transfer reduction of conjugated alkenes and an imine using polymer-supported formates Basudeb Basu, Md.Mosharef H. Bhuiyan, Pralay Das, Ismail Hossain Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . Methyl 6-hydroxy-2-methyl-1,2,3,4-tetrahydronaphthalene-5-carboxylate C13H16O3 ÏàËÆ¶È:53.8% Zeitschrift f¨¹r Naturforschung B 2009 64 699-706 Synthesis of Bicyclic Salicylates by [3+3] Cyclization of 1,3-Bis(Silyl Enol Ethers) with Cyclic 3-(Silyloxy)alk-2-en-1-ones N. Höttecke, H. Reinke, C. Fischer, and P. Langer Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . (2S,2'S)-dimethyl 3,3'-(phenazine-2,7-diyl)bis(2-((tert-butoxycarbonyl)amino)propanoate) C30H38N4O8 ÏàËÆ¶È:53.8% Heterocycles 2012 84 1345-1353 Synthesis of Substituted Phenazines via Palladium-Catalyzed Aryl Ligation Jeffrey D. Winkler,* Barry M. Twenter, and Thomas Gendrineau Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . (S)-2-[(4-hydroxybenzylidene)amino]-3-(4-hydroxyphen-yl)propionic acid methyl ester ÏàËÆ¶È:53.8% Journal of Medicinal Chemistry 2002 45 2410-2416 Inhibition of MIF Bioactivity by Rational Design of Pharmacological Inhibitors of MIF Tautomerase Activity Angeles Dios, Robert A. Mitchell, Bayan Aljabari, Jodi Lubetsky, KerryAnn O'Connor, Hong Liao, Peter D. Senter, Kirk R. Manogue, Elias Lolis, Christine Metz, Richard Bucala, David J. E. Callaway, and Yousef Al-Abed Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . methyl 3-(6-methyl-2-oxo-2H-benzo[1,4]oxazin-3-yl)propanoate C13H13NO4 ÏàËÆ¶È:53.8% Journal of Heterocyclic Chemistry 2013 50 413-416 Novel 3-(2-Oxo-2H-benzo[1,4]oxazin-3-yl)propanoates from Dimethyl-2-oxoglutarate and Test of Their Biological Activity Kamel Hachama, Mohamed Khodja, Saad Moulay, Hocine Boutoumi, Lothar Hennig and Dieter Sicker Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . methyl 3-(5-methyl-2-oxo-2H-benzo[1,4]oxazin-3-yl)propanoate C13H13NO4 ÏàËÆ¶È:53.8% Journal of Heterocyclic Chemistry 2013 50 413-416 Novel 3-(2-Oxo-2H-benzo[1,4]oxazin-3-yl)propanoates from Dimethyl-2-oxoglutarate and Test of Their Biological Activity Kamel Hachama, Mohamed Khodja, Saad Moulay, Hocine Boutoumi, Lothar Hennig and Dieter Sicker Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . (S)-tert-Butyl (1-Oxo-3-phenyl-1-((2-selenocyanatoethyl)amino)propan-2-yl)carbamate ÏàËÆ¶È:53.8% Molecules 2013 18 1963-1972 Biohybrid -Se-S- Coupling Reactions of an Amino Acid Derived Seleninate Mohannad Abdo, Zhexun Sun and Spencer Knapp Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . methyl ester of 4-hydroxyphenylpyruvic acid oxime C10H11NO4 ÏàËÆ¶È:50% Journal of Natural Products 2009 72 2049-2052 Aspergillusol A, an ¦Á-Glucosidase Inhibitor from the Marine-Derived Fungus Aspergillus aculeatus Nattha Ingavat, Jeffrey Dobereiner, Suthep Wiyakrutta, Chulabhorn Mahidol, Somsak Ruchirawat, and Prasat Kittakoop Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 1¦Â-hydroxyl-4-epigardendiol ÏàËÆ¶È:50% Phytochemistry 2002 59 537-542 Non-glycosidic iridoids from Cymbaria mongolica Jing-Qiu Dai, Zhong-Li Liu, Li Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . bungein A C16H18O4 ÏàËÆ¶È:50% Acta Botanica Yunnanica 2000 22(2) 234-236 A New Peroxide Compound from Clerodendrum bungei YANG Hui, WANGJia,MEI Shuang-Xi, SUN Han-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . Methyl 2-[(Diethoxyphosphoryl)methyl]cyclopent-1-ene-1-carboxylate ÏàËÆ¶È:50% Helvetica Chimica Acta 2009 92 823-838 Syntheses of 5-Chlorouracils/Thymines with 1-[Phosphono(Methyl/Difluoromethyl)]-1,2-Unsaturated-Moiety-Substituted Methyl Groups at N(1) and Human Thymidine Phosphorylase Inhibitory Activity Matthew R. Birck, Keith Clinch, Graeme J. Gainsford, Vern L. Schramm, Peter C. Tyler Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . compound 1i ÏàËÆ¶È:50% Molecules 1999 4 279-286 Synthetical Application of Alkyl 2-isothiocyanatocarboxylates. A Simple Synthesis of 5-Substituted-3-amino-2-thioxo-4-imidazolidinones (3-Amino-2-thiohydantoins) Lubomir Floch1, Vladimir Oremus2 and Martin Kovac Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . N-(4-methoxybenzyl)propane-1,3-diamine ÏàËÆ¶È:50% Molecules 2002 7 405-411 Synthesis of Platinum Complexes from N-Benzyl-1, 3-Propanediamine Derivatives, Potential Antineoplastic Agents Mauro V. de Almeida, Ana P. Fontes, Richard N. Berg, Eloi T. 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Khan Structure 13C NMR ̼Æ×Ä£Äâͼ |

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