| ²é¿´: 1280 | »Ø¸´: 3 | ||
| µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû | ||
wei537113ͳæ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖúÁ½¸ö»¯ºÏÎïµÄάÆÕCÆ×Êý¾Ý~~~~ллÁË~~~~~
|
|
|
»¯ºÏÎï1£º13C NMR (101 MHz, CDCl3)11.94,11.97,17.38,18.70,19.02,19.81,21.03,23.07,24.18,26.08,28.18,29.16,32.05,32.95,33.88,33.98,35.63,35.69,36.11,38.60,39.63,42.39,45.83,53.82,55.88,56.01,76.69,77.01,77.33,123.73,171.68,199.63 »¯ºÏÎï2£º 13C NMR (101 MHz, CDCl3)£º 127.49,127.68,128.68,128.91,129.04,129.18,130.19,130.55,131.96,133.49,134.27,136.09,139.17,147.34,165.50 |
» ²ÂÄãϲ»¶
281Çóµ÷¼Á£¨0805£©
ÒѾÓÐ8È˻ظ´
»·¾³ÁìÓòÈ«¹úÖØµãʵÑéÊÒÕÐÊÕ²©Ê¿1-2Ãû
ÒѾÓÐ3È˻ظ´
²ÄÁÏר˶306Ó¢Ò»Êý¶þ
ÒѾÓÐ10È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
Ò»Ö¾Ô¸Ìì½ò´óѧ»¯Ñ§¹¤ÒÕרҵ£¨081702£©315·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
302Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
26²©Ê¿ÉêÇë
ÒѾÓÐ3È˻ظ´
268Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
311Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
±»ÎÒÑÔÖУºÐÂÄ£°å²»Ç¿µ÷¸ñʽÁË£¬¼Ùר¼Ò¿ªÊ¼¹Ü¸ñʽÁË
ÒѾÓÐ4È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú ²éѯάÆÕÊý¾Ý¡£¡£¡£¡£¡£¼±¼±¼± ÔÚÏߵȡ£¡£¡£¡£¡£×·¼Ó½ð±Ò¡£¡£¡£
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú¡¿ÈçºÎ·ÖÀ뿪Á½¸öÔÚÒºÏàÉÏÏà²î0.5·ÖÖÓ³öÀ´µÄ»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÇóÖúÈçϵÄÁ½¸ö»¯ºÏÎïÈçºÎͨ¹ýÆ×ͼÐÅÏ¢À´È·Ö¤¾ßÌåÊÇÄĸö½á¹¹£¿ лл
ÒѾÓÐ27È˻ظ´
¡¾ÇóÖú¡¿Çë³æÓÑÃǰï°ï½âÒ»ÏÂÕâ¸ö»¯ºÏÎï°¡£¬ÓÐÇâÆ×£¬Ì¼Æ×ºÍÖÊÆ×Êý¾Ý
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿ÇâÆ×ºÍ̼Æ×¼ìË÷ºóÊý¾Ý¿âûÓиû¯ºÏÎ½ÓÏÂÀ´QCºÍBC¶¼Òª×öÒ»ÏÂÂð£¿
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿±£Áôʱ¼ä²»Ò»ÑùµÄÁ½¸ö»¯ºÏÎïµÄÇâÆ×̼Æ×Ò»Ñù£¿
ÒѾÓÐ13È˻ظ´
άÆÕÕ˺ÅÃÜÂë
ÒѾÓÐ18È˻ظ´
¡¾ÌÖÂÛ¡¿ÇóÖú£º£ºNOTEEXPRESS Ö±½ÓÁ¬ÏßάÆÕÊý¾Ý¿âÏÂÔØÈ«ÎÄ
ÒѾÓÐ3È˻ظ´
wei537113
ͳæ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 595.4
- É¢½ð: 7
- ºì»¨: 1
- Ìû×Ó: 147
- ÔÚÏß: 298.6Сʱ
- ³æºÅ: 1141104
- ×¢²á: 2010-11-07
- ÐÔ±ð: GG
- רҵ: Ãñ×åҩѧ
3Â¥2012-06-09 12:18:59
³æ³æÄ¾Ä¾Ð¡
гæ (СÓÐÃûÆø)
- Ó¦Öú: 24 (СѧÉú)
- ½ð±Ò: 520.3
- ºì»¨: 2
- Ìû×Ó: 69
- ÔÚÏß: 16.7Сʱ
- ³æºÅ: 1651062
- ×¢²á: 2012-02-28
- רҵ: Ò©Îﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
1...... ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 11.94,11.97,17.38,18.70,19.02,19.81,21.03,23.07,24.18,26.08,28.18,29.16,32.05,32.95,33.88,33.98,35.63,35.69,36.11,38.60,39.63,42.39,45.83,53.82,55.88,56.01,76.69,77.01,77.33,123.73,171.68,199.63 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½8289¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . ¦Â-sitostenone C29H48O ÏàËÆ¶È:90.6% Natural Product Research 2008 22 1085-1093 Isolation of antibacterial diterpenoids from Cryptomeria japonica bark Wen-Hsin Li; Shang-Tzen Chang; Shan-Chwen Chang; Hui-Ting Chang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . stigmast-4-en-3-one ÏàËÆ¶È:90.6% China Journal of Chinese Materia Medica 2009 34 1809-1811 Steroids from Monascus purpureus metabolite SHANG Xiaoya, WANG Ruolan, YI N Suqin, LI Jinjie, JIN Zonglian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ¦Â-sitostenone ÏàËÆ¶È:90.6% China Journal of Chinese Materia Medica 2008 33 405-408 Studies on phenolic compounds from Stellera chamaejasme FENG Bao, GONG Xiaojie, SHI Liying, JIAN Ge, PEI Yue-hu, WANG Yong-qi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . sitgmast-4-en-3-one ÏàËÆ¶È:90.6% China Journal of Chinese Materia Medica 2006 31 1953-1955 Chemical constitutents of Bauhinia aurea SHANG Xiaoya, LI Shuai, WANG Yinghong, WANG Sujuan, YANG Yongchun, SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . stigmast-4-en-3-one ÏàËÆ¶È:90.6% China Journal of Chinese Materia Medica 2005 30 671-674 Study on chemical constituents in rhizome of Pinellia ternata HE Ping, LI Shuai, WANG Su-juan, YANG Yong-chun, SHI Jian-gong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . stigmastan-4-en-3-one ÏàËÆ¶È:90.6% Journal of Natural Products 1990 Vol 53 1430 Stigmasterols from Typha latifolia Marina Della Greca, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Stigmast-4-en-3-one ÏàËÆ¶È:90.6% Natural Product Sciences 2008 14 100-106 Phytochemical Constituents of Schizonepeta tenuifolia Briquet Lee, Il-Kyun; Kim, Min-Ah; Lee, Seung-Young; Hong, Jong-Ki; Lee, Jei-Hyun; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (24R)-Stigmast-4-ene-3-one C29H46O2 ÏàËÆ¶È:90.6% Phytochemistry 1993 34 523-527 Steroidal constituents from mature wheat straw Elvira M.M. Gaspar, Higuinaldo J.C. das Neves Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . stigmast-4-en-3-one ÏàËÆ¶È:90.6% Korean Journal of Pharmacognosy 2000 31(1) 109-111 A Study on the Constituents from the roots of Astragalus membranaceus(Bunge) (III) Kim, Chung-Sook; Kim, Jin-Sook Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . ¦Â-sitost-4-en-3-one ÏàËÆ¶È:90.6% Korean Journal of Pharmacognosy 1996 27(1) 75-79 Phytochemical Constituents from Aconitum pseudolaeve Var. erectum Kim, Dae-Keun; Kwak, Jong-Hwan; Song, Ki-Won; Kwon, Hack-Cheol; Zee, Ok-Pyo; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . stigmasta-4-en-3-one ÏàËÆ¶È:90.6% Chinese Journal of Marine Drugs 2009 28(3) 23-28 Sterols from the mangrove plant Acanthus ilicifolius HAI Fang, T ANG Xu-li, LI Guo-qiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . ¦Â-sitostenone ÏàËÆ¶È:90.6% Chinese Journal of Marine Drugs 2008 27(1) 40-42 Studies on the chemical constituents of Nypa fruticans NAN Hai-han, YIN Hao, ZHANG Si Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . stigmasta-4-en-3-one C29H48O ÏàËÆ¶È:90.6% Chinese Journal of Marine Drugs 2007 26(6) 5-9 Studies on chemical constituents in ethanol ic extract from A-ca nt hus ilici f olius as a pharmaceutic mangrove ZHANG Liang-liang, WANG Zhan-chang, CHEN Jun-de, LIN Peng, YANG Zhi-wei, LIN Yi-ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . ¦Â-Sitostenone C29H48O ÏàËÆ¶È:90.6% Natural Product Research 2011 Vol. 25, No. 13 1243-1249 Chemical constituents from the roots of Xanthium sibiricum Suqin Kan, Guangying Chen, Changri Han, Zhong Chen, Xinming Song, Ming Ren and Hong Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . stigmasta-4-en-3-one ÏàËÆ¶È:90.6% China Journal of Chinese Materia Medica 2010 35 1137-1141 Ethyl acetate-soluble chemical constituents from whole plants of Senecio chrysanthemoides LIN Sheng; ZHANF Zhongxiao; SHEN Yunheng; LI Huiliang; SHAN Lei; LIU Runhui; XU Xike; ZHANF Weidong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . ¶¹çÞ-4-Ï©-3-ͪ ÏàËÆ¶È:90.6% Chinese Traditional and Herbal Drugs 2009 40 536-538 ÂæÍÕÌã°ê¾¥µÄ»¯Ñ§³É·ÖÑо¿ ·ëÓýÁÖ;ÎâÝí;ÀîÔÆÇï;ÐìÀöÕä;ÑîÊÀÁÖ -------------------------------------------------------------------------------- -------------------------------------------------------------------------------- 4 . 2-methyl-4-oxo-3-(1-phenyl-2-amino)vinyl-3,4-dihydroquinazoline C17H15N3O ÏàËÆ¶È:80% Journal of Heterocyclic Chemistry 2000 37 831-837 Preparation of 2-phenyl-2-hydroxymethyl-4-oxo-1,2,3,4-tetrahydroquinazoline and 2-methyl-4-oxo-3,4-dihydroquinazoline derivatives formation Pavel Hradil, Lubom¨ªr Kvapil, Jan Hlav¨¢č, Tom¨¢Š Weidlich, Anton¨ªn Lyčka and Karel Lemr Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 11-chloro-1H-dibenzo[2,3:6,7]thiepino[4,5-d]imidazole C15H10ClN2S ÏàËÆ¶È:80% Journal of Heterocyclic Chemistry 2010 47 640-656 Novel tetracyclic imidazole derivatives: Synthesis, dynamic NMR study, and anti-inflammatory evaluation Renata Rupčić, Marina Modrić, Antun Hutinec, Ana Čikoš, Barbara Stanić, Milan Mesić, Dijana Pešić and Mladen Merćep Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . N-[1-(2-chlorophenyl)-5-hydroxy-1H-pyrazol-4-yl]benzamide C16H12ClN3O2 ÏàËÆ¶È:80% Heterocycles 2007 73 555-566 Simple Approach to Some N-(5-Hydroxy-1-phenyl-1H-pyrazol-4-yl)benzamides Karmen Cucek, Amalija Golobic, and Bojan Vercek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Compound 3 ÏàËÆ¶È:80% Magnetic Resonance in Chmesitry 2005 43 1057-1062 Complete 1H and 13C NMR spectral assignment of N-aralkylsulfonamides, N-sulfonyl-1, 2, 3, 4-tetrahydroisoquinolines and N-sulfonyl-2, 3, 4, 5-tetrahydro-1H-2-benzazepines. Conformational analysis of N-[((3', 4'-dichlorophenyl)methyl)sulfonyl]-3-methyl-2, Jorge L. Jios, Gustavo P. Romanelli, Juan Carlos Autino, H¨¦ctor E. Giaccio, Helmut Duddeck and Michael Wiebcke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 2-hydroxy-1-(naphthalen-2-yl)-2-phenylethanone C18H14O2 ÏàËÆ¶È:80% Tetrahedron 2008 64 7929-7936 Enantioselective monoreduction of different 1,2-diaryl-1,2-diketones catalysed by lyophilised whole cells from Pichia glucozyma Pilar Hoyos, Giacomo Sansottera, Mar¨ªa Fern¨¢ndez, Francesco Molinari, Jos¨¦ Vicente Sinisterra, Andr¨¦s R. Alc¨¢ntara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound IIk ÏàËÆ¶È:80% Russian Journal of Organic Chemistry 2001 37 1463-1475 Tributyltin Aryl Selenides as Efficient Arylselenating Agents. Synthesis of Diaryl and Aryl Organyl Selenides I. P. Beletskaya, A. S. Sigeev, A. S. Peregudov and P. V. Petrovskii Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 2-allyl-6-methylphenyl benzoate C17H16O2 ÏàËÆ¶È:80% Tetrahedron 2012 68 2611-2620 A general route for the stereoselective synthesis of (E)-(1-propenyl)phenyl esters by catalytic CC bond isomerization Alba E. D¨ªaz-Álvarez, Pascale Crochet, Victorio Cadierno Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 2g C20H16O3 ÏàËÆ¶È:77.7% Indian Journal of Chemistry 2011 50B 593-604 Solvent free synthesis, spectral studies and antioxidant activities of some 6-substituted w-bromo-2-naphthyl ketones and their esters Thirunarayanan, G; Vanangamudi, G; Sathiyendran, V; Ravi, K Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3-{[4-Chloroyphenyl)methylene]amino}-2-phenylquinazolin-4(3H)-one C21H14N3OCl ÏàËÆ¶È:76.4% Molecules 2007 12 2413-2426 Antibacterial Activity of Some 3-(Arylideneamino)-2-phenylquinazoline-4(3H)-ones: Synthesis and Preliminary QSAR Studies Ashis K. Nanda, Subarna Ganguli and Ranadhir Chakraborty Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 2-phenyl-4-o-tolyl-2H-phthalazin-1-one C21H16N2O ÏàËÆ¶È:76.4% Chinese Chemical Letters 2010 21 538-541 An efficient chemo-and regioselective three-component synthesis of pyridazinones and phthalazinones using activated KSF L.Zare;N.O.Mahmoodi;A.Yahyazadeh;M.Mamaghani;K.Tabatabaeian; Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 2-phenyl-4-o-tolyl-2H phthalazin-1-one C21H16N2O ÏàËÆ¶È:76.4% Journal of Heterocyclic Chemistry 2011 48 864-867 An efficient one-pot synthesis of pyridazinones and phthalazinones using HY-zeolite Leila Zare, Nosratollah Mahmoodi, Asieh Yahyazadeh, Manouchehr Mamaghani and Khalil Tabatabaeian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 3-Hydroxy-4-phenyl-1H,3H-benzo[de]isochromen-1-one C18H12O3 ÏàËÆ¶È:75% Records of Natural Products 2010 4 26-30 Phenylphenalenones from Musa cv. ¡®Thepanom¡¯ (BBB) Kusuma Jitsaeng, Christian Paetz and Bernd Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 1-benzenesulfonyloxy-2,4,7-tris(N,N-dimethylaminosulfonyl)naphtha-lene C22H27N3O9S4 ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 2009 57 1257-1266 Photochemical Cleavage Reactions of 8-Quinolinyl Sulfonates in Aqueous Solution Yoshiyuki Kageyama, Ryosuke Ohshima, Kazusa Sakurama, Yoshihisa Fujiwara, Yoshifumi Tanimoto, Yasuyuki Yamada and Shin Aoki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 1-benzyl-2-bromo-4,5-diphenylimidazole C22H17BrN2 ÏàËÆ¶È:75% Journal of Heterocyclic Chemistry 2005 42 1369-1379 New calcineurin inhibiting 3-dimethylaminopropyl substituted diarylheterocycles by sonogashira reactions and catalytic hydrogenation Lunxiang Yin,J¨¹rgen Liebscher and Frank Erdmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (Z)-2-acetylamino-N-benz yl-3-(3-chl orophenyl)-2-propenamide C18H17N2O2Cl ÏàËÆ¶È:75% Heterocycles 2003 60 637-654 meta-Substituent Effects on the Photocyclization of Aryl-substituted N-Acyl-¦Á-dehydroalanine Derivatives Kei Maekawa, Hiroo Kajiwara, Yoshiyuki Iseya, Tetsutaro Igarashi, and Tadamitsu Sakurai* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . Compound 7 C16H11N3O ÏàËÆ¶È:75% Bioorganic & Medicinal Chemistry Letters 2003 13 653-656 Protective effect of imidazolopyrazinone antioxidants on ischemia/reperfusion injury Axelle Arrault, Marl¨¨ne Dubuisson, Sonia Gharbi, C¨¦cile Marchand, Tony Verbeuren, Alain Rupin, Alex Cordi, Eliete Bouskela, Jean-François Rees, Jacqueline Marchand-Brynaert Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . compound 3a C18H14F2O3S ÏàËÆ¶È:75% Tetrahedron Letters 2005 46 8273-8277 Nucleophilic difluoromethylation of carbonyl compounds using TMSCF2SO2Ph and Mg0-mediated desulfonylation Chuanfa Ni, Jinbo Hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 3,4-Diphenylpyrido[1,2-a]pyrimidinium perchlorate C20H15N2O4Cl ÏàËÆ¶È:75% Zeitschrift f¨¹r Naturforschung B 2004 59 424-430 Reactions of 3-Chloropropeniminium Salts with Aminopyridines. Synthesis of N-Pyridylpyridinium and Pyrido[1,2-a]pyrimidinium Salts U. Girreser, D. Heber, M. Rostaie-Gerylow, and M. Sch¨¹tt Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . phenyl-[2-(2-sulfanylphenylsulfanyl)phenyl]-methanol C19H14S2 ÏàËÆ¶È:75% Tetrahedron 2003 59 2083-2092 Dibenzothiepins, phthalans and phthalides from 4-heterosubstituted dibenzothiins Miguel Yus, Francisco Foubelo, Jos¨¦ V Ferr¨¢ndez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 2-hydroxy-1-(naphthalen-1-yl)-2-phenylethanone C18H14O2 ÏàËÆ¶È:75% Tetrahedron 2008 64 7929-7936 Enantioselective monoreduction of different 1,2-diaryl-1,2-diketones catalysed by lyophilised whole cells from Pichia glucozyma Pilar Hoyos, Giacomo Sansottera, Mar¨ªa Fern¨¢ndez, Francesco Molinari, Jos¨¦ Vicente Sinisterra, Andr¨¦s R. Alc¨¢ntara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 4-(2-chlorophenyl)-2-phenyl-2H phthalazin-1-one C20H13ClN2O ÏàËÆ¶È:75% Journal of Heterocyclic Chemistry 2011 48 864-867 An efficient one-pot synthesis of pyridazinones and phthalazinones using HY-zeolite Leila Zare, Nosratollah Mahmoodi, Asieh Yahyazadeh, Manouchehr Mamaghani and Khalil Tabatabaeian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . acridin-4-ylmethyl 4-chlorobenzoate C21H14NO2Cl ÏàËÆ¶È:73.6% Heterocycles 2003 60 1653-1672 Synthesis and Crystallographic Studies of New Acridinic Esters and Amides: An Efficient Synthetic Route to 4-Methyl Functionalized Acridines Julien Chiron* and Jean-Pierre Galy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . E-2,3-diphenylpropenoate C19H20O2 ÏàËÆ¶È:73.3% Molecules 2004 9 256-263 Preparation of New 2, 3-Diphenylpropenoic Acid Esters ¨C Good Yields Even for the More Hindered Z Isomers L¨¢szl¨® Boros, K¨¢roly Felföldi and Istv¨¢n P¨¢link¨® Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . 3,5-Dichloro-2-(naphthalen-1-yl)pyridine C15H9Cl2N ÏàËÆ¶È:73.3% Molecules 2009 14 3153-3160 Synthesis of Novel 3, 5-Dichloro-2-arylpyridines by Palladium Acetate-Catalyzed Ligand-Free Suzuki Reactions in Aqueous Media Huanan Hu, Changhua Ge, Anjiang Zhang and Lisheng Ding Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . 3-Benzyl-6-(3-chlorophenyl)-1,2,4-triazolo[3,4-b] [1,3,4] thiadiazole C16H11ClN4S ÏàËÆ¶È:73.3% Chemical Research in Chinese Universities 2002 18 280-283 Preparation and Spectral Characterization of 3-Benzyl-6-aryl-1,2,4-triazolo[3, 4-b][1,3,4] thiadiazoles ZHANG Li-xue, ZHANG An-jiang, CHEN Guang,CHEN Fei-yu, JIANG Yi-ping and ZHANG Zi-yi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . 1-(4-Chlorophenyl)-3-(2,4-dichlorophenyl)-2-nitro-1-propene C15H10NO2Cl3 ÏàËÆ¶È:73.3% Bioorganic & Medicinal Chemistry 2011 19 1328-1348 Synthesis and serotonin transporter activity of 1,3-bis(aryl)-2-nitro-1-propenes as a new class of anticancer agents Yvonne M. McNamara , Suzanne M. Cloonan, Andrew J. S. Knox, John J. Keating, Stephen G. Butler,G¨¹nther H. Peters, Mary J. Meegan, D. Clive Williams Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . 2-Chloro-N-[[(2-chlorobenzoyl)amino](4-chlorophenyl)methyl]benzamide C21H15N2O3Cl3 ÏàËÆ¶È:73.3% Canadian Journal of Chemistry 2008 86 32-38 A convenient and efficient protocol for the synthesis of symmetrical |
2Â¥2012-06-09 10:12:07
³æ³æÄ¾Ä¾Ð¡
гæ (СÓÐÃûÆø)
- Ó¦Öú: 24 (СѧÉú)
- ½ð±Ò: 520.3
- ºì»¨: 2
- Ìû×Ó: 69
- ÔÚÏß: 16.7Сʱ
- ³æºÅ: 1651062
- ×¢²á: 2012-02-28
- רҵ: Ò©Îﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
wei537113: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2012-06-09 17:16:05
wei537113: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2012-06-09 17:16:05
|
Öмä·Ö¿ªµÄ£¬Ç°16¸öÊǵÚÒ»¸ö»¯ºÏÎïµÄ£¬ºóÃæ´Ó4¿ªÊ¼Êǵڶþ¸ö»¯ºÏÎïµÄ£¬ÎÒÏÖÔڰѵڶþ¸ö»¯ºÏÎïµÄ1-3¸øÄ㸽ÉÏ¡£ÁíÍ⣬ÒÔºó±£ÁôСÊýµãһ룬Á½Î»ºÜÂý¡£ ²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 127.49,127.68,128.68,128.91,129.04,129.18,130.19,130.55,131.96,133.49,134.27,136.09,139.17,147.34,165.50 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½5920¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 2-Chloro-N-[[(2-chlorobenzoyl)amino](2,4-dichlorophenyl)methyl]benzamide C21H14N2O2Cl4 ÏàËÆ¶È:80% Canadian Journal of Chemistry 2008 86 32-38 A convenient and efficient protocol for the synthesis of symmetrical N,N'-alkylidine bisamides by sulfamic acid under solvent-free conditions Nagarajan Panneer Selvam, Sundar Saranya, and Paramasivan T. Perumal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 2-Chloro-N-[[(2-chlorobenzoyl)amino](2-chlorophenyl)methyl]benzamide C21H15N2O3Cl3 ÏàËÆ¶È:80% Canadian Journal of Chemistry 2008 86 32-38 A convenient and efficient protocol for the synthesis of symmetrical N,N'-alkylidine bisamides by sulfamic acid under solvent-free conditions Nagarajan Panneer Selvam, Sundar Saranya, and Paramasivan T. Perumal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . N-Benzoylamino(4-fluorophenyl)methyl benzamide C21H17FN2O2 ÏàËÆ¶È:80% Canadian Journal of Chemistry 2011 89 555¨C561 Silica-supported barium chloride (SiO2¨CBaCl2) ¡ªEfficient and heterogeneous catalyst for the environmentally friendly preparation of N, N'-alkylidene bisamides under solvent-free conditions Mohammad Reza Mohammad Shafiee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 2-methyl-4-oxo-3-(1-phenyl-2-amino)vinyl-3,4-dihydroquinazoline C17H15N3O ÏàËÆ¶È:80% Journal of Heterocyclic Chemistry 2000 37 831-837 Preparation of 2-phenyl-2-hydroxymethyl-4-oxo-1,2,3,4-tetrahydroquinazoline and 2-methyl-4-oxo-3,4-dihydroquinazoline derivatives formation Pavel Hradil, Lubom¨ªr Kvapil, Jan Hlav¨¢č, Tom¨¢Š Weidlich, Anton¨ªn Lyčka and Karel Lemr Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 11-chloro-1H-dibenzo[2,3:6,7]thiepino[4,5-d]imidazole C15H10ClN2S ÏàËÆ¶È:80% Journal of Heterocyclic Chemistry 2010 47 640-656 Novel tetracyclic imidazole derivatives: Synthesis, dynamic NMR study, and anti-inflammatory evaluation Renata Rupčić, Marina Modrić, Antun Hutinec, Ana Čikoš, Barbara Stanić, Milan Mesić, Dijana Pešić and Mladen Merćep Structure 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2012-06-09 13:07:36













»Ø¸´´ËÂ¥