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wenjuan9716½ð³æ (СÓÐÃûÆø)
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̼Æ×Ðźţº µÚÒ»¸ö15.171,19.398,19.575,21.119,23.869,24.324,26.206,27.361,28.250,29.695,31.730,31.948,32.714,34.017,34.857,36.171,37.307,37.679,42.369,43.086,56.825,71.839,78.942,109.605 µÚ¶þ¸ö 12.499,12.679,19.538,19.751,19.938,20.477,21.817,23.950,25.029,26.997,29.048,30.048,30.796,32.609,32.706,34.769,36.908,37.466,38.024,39.888,40.499,43.025,46.610,50.907,56.811,57.378,63.414,72.289,75.867,78.691,78.964,79.136,103.130,141.478 |
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xiaoxiao270: ½ð±Ò+4 2013-02-25 19:41:33
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xiaoxiao270: ½ð±Ò+4 2013-02-25 19:41:33
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»¯ºÏÎï1 ²éѯ½á¹û£º¹²²éµ½5446¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 21 ÏàËÆ¶È:76% Organic Magnetic Resonance 1983 21 305-309 Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 29 ÏàËÆ¶È:76% Organic Magnetic Resonance 1983 21 305-309 Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (20R)-25-thia-27-norcholest-5-en-3¦Â-ol C28H50OSiS ÏàËÆ¶È:72% Bioorganic & Medicinal Chemistry 2012 20 4064-4081 Substrate analog studies of the ¦Ø-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1 Jonathan B. Johnston, Arti A. Singh, Anaelle A. Clary, Chiung-Kuan Chen, Patricia Y. Hayes, Sharon Chow, James J. De Voss, Paul R. Ortiz de Montellano Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 26 ÏàËÆ¶È:72% Organic Magnetic Resonance 1983 21 305-309 Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound II ÏàËÆ¶È:70.8% Russian Journal of Organic Chemistry 2009 45 78-86 Synthesis of nitrogen- and oxygen-containing macrocycles by palladium-catalyzed amination of 3,24-bis(6-chloropyridin-2-yloxy)cholane A. D. Averin, E. R. Ranyuk, N. V. Lukashev, A. K. Buryak and I. P. Beletskaya Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (20R)-24-bromochol-5-en-3¦Â-ol C24H39BrO ÏàËÆ¶È:70.8% Bioorganic & Medicinal Chemistry 2012 20 4064-4081 Substrate analog studies of the ¦Ø-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1 Jonathan B. Johnston, Arti A. Singh, Anaelle A. Clary, Chiung-Kuan Chen, Patricia Y. Hayes, Sharon Chow, James J. De Voss, Paul R. Ortiz de Montellano Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Á-Hydroxy-5¦Â-cholan-24-oic acid lithocholic acid C24H40O3 ÏàËÆ¶È:70.8% Organic Magnetic Resonance 1977 9 439-464 13C N.m.r. Spectra of steroids¡ªA Survey and Commentary J.W.Blunt and J.B.Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (20R)-3¦Â-(tert-butyldimethylsilyloxy)-24-bromochol-5-ene C30H53BrOSi ÏàËÆ¶È:70.3% Bioorganic & Medicinal Chemistry 2012 20 4064-4081 Substrate analog studies of the ¦Ø-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1 Jonathan B. Johnston, Arti A. Singh, Anaelle A. Clary, Chiung-Kuan Chen, Patricia Y. Hayes, Sharon Chow, James J. De Voss, Paul R. Ortiz de Montellano Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ¡÷ 9(11),22-24-norchlolest-3¦Â-ol ÏàËÆ¶È:69.2% Steroids 2010 75 834-847 Synthesis of cytotoxic novel 9,11-secosterol analogs: Structure/activity studies Boonsong Kongkathip, Anuch Hasakunpaisarn, Suthinee Boonananwong, Ngampong Kongkathip Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . N-(2-thioethyl)-3¦Á-hydroxy-5¦Â-cholan-24-amide C26H45NO2S ÏàËÆ¶È:69.2% Steroids 2012 77 193-203 Bile acid¨Ccysteamine conjugates: Structural properties, gelation, and toxicity evaluation Virpi Noponen, Heini Belt, Manu Lahtinen, Arto Valkonen, Hannu Salo, Jitka Ulrichov¨¢, Ad¨¦la Galand¨¢kov¨¢, Elina Sievänen Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . stigmast-5-ene-3¦Â,17¦Á-diol C29H50O2 ÏàËÆ¶È:68.9% Journal of Asian Natural products Research 2010 12 424-428 New cytotoxic steroids from the fruits of Syzygium siamense Parinuch Chumkaew; Shigeru Kato; Kan Chantrapromma Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . nitidasin C25H40O3 ÏàËÆ¶È:68% Chemical & Pharmaceutical Bulletin 1997 45 1717-1719 NITIDASIN, A NOVEL SESTERTERPENOID, FROM THE PERUVIAN FOLK MEDICINE "HERCAMPURI" (GENTIANELLA NITIDA) Nobuo KAWAHARA,Masato NOZAWA,Diana FLORES,Pablo BONILLA,Setsuko SEKITA,Motoyoshi SATAKE and Ken-ichi KAWAI Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Sodium 3¦Á-hydroxy-5¦Â-cholan-24-ol sulfate C24H41SO5 ÏàËÆ¶È:68% Steroids 2011 76 291-300 Synthesis and olfactory activity of unnatural, sulfated 5-bile acid derivatives in the sea lamprey (Petromyzon marinus) Aaron C. Burns, Peter W. Sorensen, Thomas R. Hoye Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 8 ÏàËÆ¶È:68% Organic Magnetic Resonance 1983 21 305-309 Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (24S)-24-methylcholest-5-ene-3¦Â,25-diol ÏàËÆ¶È:67.8% Chemical & Pharmaceutical Bulletin 1983 31 1848-1855 Marine Sterols. XI. Polyhydroxysterols of the Soft Coral Sarcophyton glaucum : Isolation and Synthesis of 5¦Á-Cholestane-1¦Â, 3¦Â, 5, 6¦Â-tetrol MASARU KOBAYASHI,TAKAAKI HAYASHI,KOJI HAYASHI,MASATO TANABE,TAKASHI NAKAGAWA and HIROSHI MITSUHASHI Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . daucosterol ÏàËÆ¶È:67.8% China Journal of Chinese Materia Medica 2002 27 752-754 Studies on the Chemical Constituents in Radix Astilbes Chinensis SUN Hongxiang, YE Yiping, YANG Ke Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (24S)-24¦Á-¼×»ùµ¨çÞ-5-Ï©-3¦Â,25-¶þ´¼((24S)-24¦Á-methylcholest-5-en-3¦Â,25-diol) C28H48O2 ÏàËÆ¶È:67.8% Chinese Journal of Marine Drugs 2002 21(1) 5-7,57 Chemical studies on the soft coral lobophytum j aeckel Tix. -Dur. WANG Ming-yan, ZENG Long-mei, SU Jing-yu Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Alkesterol A C28H44O2 ÏàËÆ¶È:67.8% Journal of Asian Natural products Research 2010 12 752-759 C28 sterols with a cyclopentane ring at C-22 and 26 from cape gooseberry (berries of Physalis pubeacens L.) Qiong-Ming Xu; Yan-Li Liu; Yu-Lin Feng; Xiao-Ran Li; Shi-Lin Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (24R)-[26-2H3]-24-methylcholestan-3¦Â-ol 12/[26-2H3]campestanol ÏàËÆ¶È:67.8% Chemistry of Natural Compounds 2012 48 606-609 Synthesis of [26-2H3]-campesterin and [26-2H3]-campestanol, deuterated analogs of biosynthetic precursors of 28C-brassinosteroids V. A. Khripach, V. N. Zhabinskii, Yu. V. Ermolovich and O. V. Gulyakevich Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . cholesterol ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 2000 36 595-598 13C NMR SPECTRA OF FUNCTIONALLY SUBSTITUTED 3 ¦Â-CHLORODERIVATIVES OF CHOLESTEROL AND ¦Â -SITOSTEROL N. V. Kovganko, Zh. N. Kashkan, and E. V. Borisov Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . pythocholic lactone C24H38O4 ÏàËÆ¶È:66.6% Acta Pharmaceutica Sinica 1992 27 674-678 STUDIES ON CHEMICAL CONSTITUENTS OF THE GALL OF PYTHON MOLURUS BIVITTATUS SCHLEGEL YJ You; JG Lin; LF Ji Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 3-Oxo-5¦Â-cholan-24-oic acid ÏàËÆ¶È:66.6% Steroids 2003 68 1157-1161 Synthesis of ester-linked lithocholic acid dimers Lutfun Nahar, Alan B. Turner Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-02-25 19:24:47
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wenjuan9716: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-02-25 20:48:38
wenjuan9716: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-02-25 20:48:38
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»¯ºÏÎï2 ²éѯ½á¹û£º¹²²éµ½6741¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Daucosterol C35H60O6 ÏàËÆ¶È:97.1% Acta Botanica Yunnanica 1997 19(1) 92-96 STUDY ON CHEMICAL CONSTITUENTS OF SAUSSUREA LAPPA ¢ò Yang Hui, ¡¡Xie J inlun,¡¡Sun Handong Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-Sitosterol ¦Â-D-glucopyranoside C35H60O6 ÏàËÆ¶È:97.1% Chemistry of Natural Compounds 2007 43 358-359 TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXV. STEROLS AND TRITERPENOIDS FROM Astragalus orbiculatus I. M. Isaev, R. P. Mamedova, M. A. Agzamova, and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Â-Sitosterol Glucoside ÏàËÆ¶È:97.1% Chemistry of Natural Compounds 1991 27 603-606 TRITERPENE GLYCOSIDES OF Hedera taurica VII. STRUCTURES OF TAUEOSIDES A AND D FROM THE LEAVES OF CRIMEAN IVY V. I. Grishkovets, N. V. Tolkacheva, A. S. Shashkov,and V. Ya. Chirva Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . daucosterol ÏàËÆ¶È:97.1% Acta Botanica Sinica 1999 41 107-110 Chemical constituents of the Anemone tomentosa Root Wang Jun-Ru, Peng Shu-Lin, Wang Ming-Kui, Feng Jun-Tao, Ding Li-Sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . daucosterol ÏàËÆ¶È:97.1% China Journal of Chinese Materia Medica 2005 30 1340-1342 Studies on chemical constituents from flowers of Apocynum venetum CHEN Long, DU Lijun, DING Yi, XISNG Dongming , WANG Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ºúÂܲ·ÜÕ ÏàËÆ¶È:97.1% China Journal of Chinese Materia Medica 2005 30 153-154 ²ØÒ©¶ÌËëÍöú²Ý»¯Ñ§³É·ÖÑо¿ ÑîÔÆÉÑ, ºÎ Àó, Ñ÷, Ê·¸ß·å, ³Èó»ª Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . daucosterol ÏàËÆ¶È:97.1% China Journal of Chinese Materia Medica 2004 29 741-758 Studies on chemical constituents in root of Paeonia sinjiangensis SONG Zhaohui, WANG Baode, BA Hang, TONG Xiaotian, ZHU Dayuan, JIANG Fuxiang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-sitosterol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:97.1% China Journal of Chinese Materia Medica 2001 26 43-47 Studies on Chemical Constituents from Buddleja lindleyana Fert LU Jianghai, ZHAO Yuying, QIAO Liang, FANG Yiou, HUANG Qinan Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . daucosterol ÏàËÆ¶È:97.1% China Journal of Chinese Materia Medica 2001 26 45-46 Chemical Constituents of Gymnotheca involucrata Pei YANG Weili, TIAN Jun, DING Lisheng Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-sitosterol ÏàËÆ¶È:97.1% China Journal of Chinese Materia Medica 1996 21 104-105 Chemical Constituents of Coleus carnosifolius Dunn. Mu Qing, Li Chaoming and Sun Handong Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . daucosterol C35H60O6 ÏàËÆ¶È:97.1% China Journal of Chinese Materia Medica 1992 17 36-38 Studies on the Chemical Constituents of Actinidia arguta(Sieb.et Zuce.)Planch.ex Miquel Shi Yue and Wang Huili, Ma Bingru Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . daucosterol ÏàËÆ¶È:97.1% China Journal of Chinese Materia Medica 1992 17 737-739 Studies on the Chemical Constituents of Drynotria propinqua(Wall)J.Sm Liu Songqiang and Xiao Zhuoyin Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ¦Â-sitosteryl-3-O-¦Â-glucopiranoside ÏàËÆ¶È:97.1% Phytochemistry 2000 53 417-422 Steroidal alkaloids from Cryptolepis obtusa Alexandra Paulo, M. Luisa Jimeno, Elsa T. Gomes, Peter J. Houghton Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Â-sitosterol-3-O-glucoside ÏàËÆ¶È:97.1% Natural Product Sciences 1998 4 263-267 Constituents from Syzygium aromaticum Merr. et Perry Son, Kun-Ho; Kwon, Soon-Youl; Kim, Hyun-Pyo; Chang, Hyeun-Wook; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Â-sitosterol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:97.1% Natural Product Sciences 2000 6 135-138 Antioxidative Constituents from the Seeds of Cuscuta chinensis Kwon, Yong-Soo; Chang, Bok-Sim; Kim, Chang-Min Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Daucosterol ÏàËÆ¶È:97.1% Natural Product Sciences 2007 13 332-336 Norsesquiterpene and Steroid Constituents of Humulus japonicus Yu, Byung-Chul; Yang, Min-Cheol; Lee, Kyu-Ha; Kim, Ki-Hyun; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3-O-¦Â-Glucosylsitosterol ÏàËÆ¶È:97.1% Phytochemistry 1994 36 221-223 Furocoumarins from the rhizomes of Dorstenia brasiliensis Ricardo M. Kuster, Robson R. Bernardo, Antonio J.R. Da Silva, Jos¨¦ P. Parente, Walter B. Mors Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 3-O-¦Â-D-glucopyranosylsitosterol ÏàËÆ¶È:97.1% Phytochemistry 1992 31 1317-1320 Pomolic acid derivatives from the rootof Sanguisorba officinalis Cheng, D. and Cao, X. Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ¦Â-Sitosterol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:97.1% Korean Journal of Pharmacognosy 2007 38(1) 67-70 Isolation of Isoprenoidal Compounds from the Stems of Acer tegmentosum Max Hur, Jong-Moon; Jun, Mi-Ra; Yang, Eun-Ju; Choi, Sun-Ha; Park, Jong-Cheol; Song, Kyung-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-Sitosterol 3-O-¦Â-glucoside ÏàËÆ¶È:97.1% Korean Journal of Pharmacognosy 2007 38(1) 76-83 Triterpenoids and Flavonoids Isolated from the Leaves of Alnus firma Yu, Young-Beob; Nakamura, Norio; Miyashiro, Hirotsugu; Hattori, Masao; Park, Jong-Cheol Structure 13C NMR ̼Æ×Ä£Äâͼ |
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