| ²é¿´: 998 | »Ø¸´: 3 | ||
341176½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
̼Æ×ÇóÖú ¼±Óà ÒÑÓÐ1È˲ÎÓë
|
| ̼Æ×Êý¾Ý£ºÈܼÁ,ë®´ú¼×´¼£º167.82, 158.70, 156.26, 137.30, 131.18, 104.36, 102.04, 81.25, 78.73, 74.48, 60.73, 56.25, 39.01, 38.04, 19.13, 13.97 |
» ²ÂÄãϲ»¶
070300»¯Ñ§Ñ§Ë¶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
0854¿ØÖƹ¤³Ì 359Çóµ÷¼Á ¿É¿çרҵ
ÒѾÓÐ8È˻ظ´
¹ú×Ô¿ÆÃæÉÏ»ù½ð×ÖÌå
ÒѾÓÐ6È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁÏÓ뻯¹¤Ò»Ö¾Ô¸Äϲý´óѧ327Çóµ÷¼ÁÍÆ¼ö
ÒѾÓÐ8È˻ظ´
0703 ÎïÀí»¯Ñ§µ÷¼Á
ÒѾÓÐ5È˻ظ´
»¯Ñ§¹¤³Ì321·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
0703»¯Ñ§µ÷¼Á 290·ÖÓпÆÑоÀú£¬ÂÛÎÄÔÚͶ
ÒѾÓÐ7È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¡¼±£¡Ð»Ð»£¡
ÒѾÓÐ5È˻ظ´
ºË´ÅÇâÆ×µÄ·ÖÎö
ÒѾÓÐ5È˻ظ´
Ç×°®µÄ³æÓÑÃÇ ¹òÇó½âÆ×(̼Æ× ÇâÆ× ÖÊÆ×£© ¼±
ÒѾÓÐ19È˻ظ´
άÆÕÇóÖú£¬Ð»Ð»£¡£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
ÇóÖúÇâÆ×̼Æ× ·ÖÎö~~~
ÒѾÓÐ4È˻ظ´
ºË´Å̼Æ×·åÖµ²»Ã÷ÏÔµÄÔÒò¼°½â¾ö·½·¨
ÒѾÓÐ6È˻ظ´
¡¾ÇóÖú¡¿·ÖÀëÌá´¿µÃµ½µÄ»¯ºÏÎï¼òµ¥ÇâÆ×ºÍ̼Æ×½âÎö
ÒѾÓÐ10È˻ظ´
ÄÄÀïÄÜ¿ìËÙ´òÇâÆ× ̼Æ× ¼±Óà ÎÒÃǺ˴ݵÁË Ð»Ð»
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿Çë³æÓÑÃǰï°ï½âÒ»ÏÂÕâ¸ö»¯ºÏÎï°¡£¬ÓÐÇâÆ×£¬Ì¼Æ×ºÍÖÊÆ×Êý¾Ý
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿¹ØÓÚ̼Æ×Öп¨±ö̼µÄλÖÃ
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿¼±£¡£¡£¡¼±£¡£¡ÇóÖúºË´Å¹²ÕñµÄ̼Æ×ÇâÆ×½âÎö
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿ë®´ø»¯ºÏÎï̼Æ× Çó½âÊÍ
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú¸÷λ ̼Æ×ÉϵĶ˻ù̼ºÍÌǵÄ×Ü̼Êý¶Ô²»ÉÏÊÇÔõô»ØÊ ÏÈлÀ²£¡
ÒѾÓÐ26È˻ظ´
¡¾ÇóÖú¡¿Çë½ÌÓÃʲôÈí¼þ¿ÉÒÔÐÞ¸ÄÇâÆ×ºÍ̼Æ×µÄÆ×ͼ£¿
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿Ì¼Æ×ÖÐȱÉÙÒÔôÊ»ù̼Êý¾Ý
ÒѾÓÐ12È˻ظ´
¡¾ÇóÖú¡¿Ì¼Æ×È¥ñîÎÊÌâ
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú¡¿ºË´ÅÇâÆ×»òÕß̼Æ×ÈçºÎ¿´º¬Á¿
ÒѾÓÐ12È˻ظ´
¡¾ÇóÖú¡¿²úÆ·ºË´ÅÇâÆ×̼Æ×´ò³öÀ´¶¼¶Ô£¬µ«ÊÇÒºÏà´ò³öÀ´ÂÒÆß°ËÔã
ÒѾÓÐ21È˻ظ´
¡¾ÇóÖú¡¿´ò̼Æ×ºÍÇâÆ×£¬ÎÒµÄÑùÆ·¹»²»¹»°¡
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú¡¿Çë¸ßÊÖ°ïÎÒÕÒѪ½ßºìËØ£¨dracorubin£©µÄ̼Æ×¼°ÇâÆ×£¬ºìÍâͼÆ×£¡
ÒѾÓÐ5È˻ظ´
·çÐÐÕß007
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
341176: ½ð±Ò+2, ¡ïÓаïÖú, ¸Ð¾õ²»ÊǺÜÏêϸ£¬²»¹ý»¹ÊÇллÁË£¬ÐÁ¿àÁË 2014-07-02 10:28:21
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
341176: ½ð±Ò+2, ¡ïÓаïÖú, ¸Ð¾õ²»ÊǺÜÏêϸ£¬²»¹ý»¹ÊÇллÁË£¬ÐÁ¿àÁË 2014-07-02 10:28:21
|
²éѯ½á¹û£º¹²²éµ½1¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . drimane-3,8,11,12-tetraol C15H28O4 ÏàËÆ¶È:50% Mycology 2011 2 30-36 New sesquiterpenes from Marasmius cladophyllus Jin Meng, Yao-Yao Li, Yi-Xin Ou, Long-Feng Song, Chun-Hua Lu & Yue-Mao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-07-02 10:08:46
341176
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 30 (СѧÉú)
- ½ð±Ò: 1006.9
- É¢½ð: 295
- ºì»¨: 9
- Ìû×Ó: 410
- ÔÚÏß: 238.5Сʱ
- ³æºÅ: 1145937
- ×¢²á: 2010-11-13
- ÐÔ±ð: GG
- רҵ: º£ÑóÒ©Îï
3Â¥2014-07-02 10:16:18
·çÐÐÕß007
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
|
ÈܼÁÊÇë®´ú¼×´¼²éµ½µÄÖ»ÓÐÒ»ÖÖ£¬ÎÒÏÖÔÚ¸øÄãÓÃÈ«²¿ÈܼÁ²éµÄ½á¹û ²éѯ½á¹û£º¹²²éµ½35¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . monocerin ÏàËÆ¶È:100% Journal of Natural Products 2008 71(6) 1078-1081 Bioactive Isocoumarins Isolated from the Endophytic Fungus Microdochium bolleyi Wen Zhang, Karsten Krohn, Siegfried Draeger, and Barbara Schulz Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . monocerin C16H20O6 ÏàËÆ¶È:100% Journal of Natural Products 2008 71(9) 1657-1659 11-Hydroxymonocerin from the Plant Endophytic Fungus Exserohilum rostratum Ruengrit Sappapan, Damrong Sommit, Nattaya Ngamrojanavanich, Somchai Pengpreecha, Suthep Wiyakrutta, Nongluksna Sriubolmas, and Khanitha Pudhom Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (12S)-12-hydroxymonocerin C16H20O7 ÏàËÆ¶È:81.2% Journal of Natural Products 2008 71(6) 1078-1081 Bioactive Isocoumarins Isolated from the Endophytic Fungus Microdochium bolleyi Wen Zhang, Karsten Krohn, Siegfried Draeger, and Barbara Schulz Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (12S)-12-hydroxymonocerin C16H20O7 ÏàËÆ¶È:81.2% Tetrahedron 2013 69 11025-11030 Biomimetically inspired total synthesis of (12S)-12-hydroxymonocerin and (12R)-12-hydroxymonocerin Bowen Fang, Xingang Xie, Peng Jing, Changgui Zhao, Huilin Li, Haichen Ma, Xuegong She Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (12S)-12-hydroxymonocerin ÏàËÆ¶È:81.2% RSC Advances 2013 3 17717-17725 Total synthesis of (12R)- and (12S)-12-hydroxymonocerins: stereoselective oxylactonization using a chiral hypervalent iodine(III) species Morifumi Fujita, Kazuhiro Mori, Mio Shimogaki and Takashi Sugimura Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (12R)-12-hydroxymonocerin C16H20O7 ÏàËÆ¶È:75% Journal of Natural Products 2008 71(6) 1078-1081 Bioactive Isocoumarins Isolated from the Endophytic Fungus Microdochium bolleyi Wen Zhang, Karsten Krohn, Siegfried Draeger, and Barbara Schulz Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (12R)-12-hydroxymonocerin C16H20O7 ÏàËÆ¶È:75% Tetrahedron 2013 69 11025-11030 Biomimetically inspired total synthesis of (12S)-12-hydroxymonocerin and (12R)-12-hydroxymonocerin Bowen Fang, Xingang Xie, Peng Jing, Changgui Zhao, Huilin Li, Haichen Ma, Xuegong She Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (12R)-12-hydroxymonocerin ÏàËÆ¶È:75% RSC Advances 2013 3 17717-17725 Total synthesis of (12R)- and (12S)-12-hydroxymonocerins: stereoselective oxylactonization using a chiral hypervalent iodine(III) species Morifumi Fujita, Kazuhiro Mori, Mio Shimogaki and Takashi Sugimura Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . isocoumarin C16H22O7 ÏàËÆ¶È:68.7% Journal of Natural Products 2008 71(6) 1078-1081 Bioactive Isocoumarins Isolated from the Endophytic Fungus Microdochium bolleyi Wen Zhang, Karsten Krohn, Siegfried Draeger, and Barbara Schulz Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 11-hydroxymonocerin C16H20H7 ÏàËÆ¶È:68.7% Journal of Natural Products 2008 71(9) 1657-1659 11-Hydroxymonocerin from the Plant Endophytic Fungus Exserohilum rostratum Ruengrit Sappapan, Damrong Sommit, Nattaya Ngamrojanavanich, Somchai Pengpreecha, Suthep Wiyakrutta, Nongluksna Sriubolmas, and Khanitha Pudhom Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . diethyl 1-(4-methoxyphenyl)-2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate C26H28N2O7 ÏàËÆ¶È:56.2% Tetrahedron 2013 69 5242-5247 Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . diethyl 4-(4-chlorophenyl)-1-(4-methoxy-phenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate C26H28ClNO5 ÏàËÆ¶È:56.2% Tetrahedron 2013 69 5242-5247 Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . diethyl 4-(furan-2-yl)-1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate C24H27NO6 ÏàËÆ¶È:56.2% Tetrahedron 2013 69 5242-5247 Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 4 C18H22O7 ÏàËÆ¶È:55.5% Journal of Natural Products 2008 71(9) 1657-1659 11-Hydroxymonocerin from the Plant Endophytic Fungus Exserohilum rostratum Ruengrit Sappapan, Damrong Sommit, Nattaya Ngamrojanavanich, Somchai Pengpreecha, Suthep Wiyakrutta, Nongluksna Sriubolmas, and Khanitha Pudhom Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . diethyl 4-(2-cyanophenyl)-1-(4-methoxy-phenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate C27H28N2O5 ÏàËÆ¶È:52.9% Tetrahedron 2013 69 5242-5247 Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 8¦Á,9¦Á-epoxyparthenolide C15H18O4 ÏàËÆ¶È:50% Fitoterapia 2004 75 573-576 Germacranolides from Anvillea radiata B. El Hassany, F. El Hanbali, M. Akssira, F. Mellouki,A. Haidourb, A.F. Barrero Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 6-methyl-7-acetyl-1,8-dihydroxy-3-methoxy naphthalene-1-O-¦Â-D(L)-glucoside C20H25O9 ÏàËÆ¶È:50% Molecules 2012 17 843-850 Two Novel Naphthalene Glucosides and an Anthraquinone Isolated from Rumex dentatus and Their Antiproliferation Activities in Four Cell Lines Hui Zhang, Zengjun Guo, Nan Wu, Wenming Xu, Ling Han, Nan Li and Yanxia Han Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . diethyl 1,4-dihydro-2,6-dimethyl-4-(4-methoxyphenyl)pyridine-3,5-dicarboxylate C20H25NO5 ÏàËÆ¶È:50% Indian Journal of Chemistry Section B 2007 46B 331-335 Cu(OTf)₂ Catalyzed high yield synthesis of Hantzsch 1,4-dihydropyridines Paraskar,Abhimanyu S; Sudalai,Arumugam Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . diethyl 1,4-dihydro-2,6-dimethyl-4-(2-methoxyphenyl)pyridine-3,5-dicarboxylate C20H25NO5 ÏàËÆ¶È:50% Indian Journal of Chemistry Section B 2007 46B 331-335 Cu(OTf)₂ Catalyzed high yield synthesis of Hantzsch 1,4-dihydropyridines Paraskar,Abhimanyu S; Sudalai,Arumugam Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ethyl 6-methoxy-3-methylquinaldate C14H15NO3 ÏàËÆ¶È:50% Heterocycles 2005 66 611-619 One-Step Synthesis of Ethyl Quinaldates by Lewis Acid Catalyzed Three-Component Coupling Reaction of Aromatic Amines, Aliphatic Aldehydes and Ethyl Glyoxylate Takashi Inada, Takayuki Nakajima, and Isao Shimizu* Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . torachrysone-8-O-¦Â-D-glucopyranoside ÏàËÆ¶È:50% Journal of Shenyang Pharmaceutical University 2009 26 536-538 Chemical cnstituents of Caulis Polygoni Multiflori (the stem of Polygonum multif lorum Thunb.) LIANG Yan, TIAN Wei-xi, MA Xiao-feng Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Phomopsinone A C12H16O4 ÏàËÆ¶È:50% European Journal of Organic Chemistry 2012 1783-1789 Phomopsinones A¨CD: Four New Pyrenocines from Endophytic Fungus Phomopsis sp. Hidayat Hussain, Karsten Krohn, Ishtiaq Ahmed, Siegfried Draeger, Barbara Schulz, Sebastiano Di Pietro and Gennaro Pescitelli Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . curvupallide A C14H17NO5 ÏàËÆ¶È:50% Tetrahedron 1995 51 4947-4952 Curvupallides, a new class of alkaloids from the fungus Curvularia pallescens Wolf-Rainer Abraham, Holger Meyer, Dawit Abate Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 6-(4-bromobenzyl)-5-ethyl-2-(4-methoxyphenylcarbonylmethylthio)pyrimidin-4(3H)-one C22H21BrN2O3S ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 3887-3894 Synthesis and biological evaluation of novel 6-substituted 5-alkyl-2-(arylcarbonylmethylthio)pyrimidin-4(3H)-ones as potent non-nucleoside HIV-1 reverse transcriptase inhibitors Yue-Ping Wang, Fen-Er Chen, Erik De Clercq, Jan Balzarini, Christophe Pannecouque Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . (R)-ethyl 2-(3-methoxyphenoxy)propanoate ÏàËÆ¶È:50% European Journal of Organic Chemistry 2011 176-182 Preparation of Novel Chiral Non-Racemic Diselenides and Applications in Asymmetric Synthesis Liwei Zhao, Zhong Li and Thomas Wirth Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 8 C21H26O9S ÏàËÆ¶È:50% European Journal of Organic Chemistry 2010 5100-5107 Formal Total Synthesis of (¨C)-Raphidecursinol B Sanjit Kumar Das, Sajal Kumar Das and Gautam Panda Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 4-ethyl 3,5-dimethyl 1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,4,5-tricarboxylate C21H25NO7 ÏàËÆ¶È:50% Tetrahedron 2013 69 5242-5247 Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . triethyl 1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,4,5-tricarboxylate C23H29NO7 ÏàËÆ¶È:50% Tetrahedron 2013 69 5242-5247 Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 4-ethyl 3,5-diisopropyl 1-(4-methoxyphen-yl)-2,6-dimethyl-1,4-dihydropyridine-3,4,5-tricarboxylate C25H33NO7 ÏàËÆ¶È:50% Tetrahedron 2013 69 5242-5247 Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 3,5-dibenzyl 4-ethyl 1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,4,5-tricarboxylate C33H33NO7 ÏàËÆ¶È:50% Tetrahedron 2013 69 5242-5247 Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng, Run-tao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . drimane-3,8,11,12-tetraol C15H28O4 ÏàËÆ¶È:50% Mycology 2011 2 30-36 New sesquiterpenes from Marasmius cladophyllus Jin Meng, Yao-Yao Li, Yi-Xin Ou, Long-Feng Song, Chun-Hua Lu & Yue-Mao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . ethyl 3-(4-cyano-3-hydroxy-5-{[(4-methylphenyl)methyl]sulfanyl}thiophen-2-yl)-3-oxopropanoate C18H17NO4S2 ÏàËÆ¶È:50% Tetrahedron 2013 69 9648-9655 New regio-selective method of combinatorial synthesis of substituted thiophenes, thieno[3,2-b]pyridines and other heterocycles via combination of ¡®domino¡¯-type reactions Original Research Article Andrey A. Zubarev, Anatoliy M. Shestopalov, Natalia A. Larionova, Lyudmila A. Rodinovskaya, Alexander A. Shestopalov Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . N,N-diethyl-4-(tert-butyldimethylsilyloxy)-6-iodo-1,3-benzodioxole-5-carboxamide C18H28INO4Si ÏàËÆ¶È:50% European Journal of Organic Chemistry 2009 2009 4666-4673 Convergent Synthesis of Pancratistatin from Piperonal and Xylose Johan Hygum Dam and Robert Madsen Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . 2-¦Â-D-glucopyranosyloxy-6-methoxybenzoate ÏàËÆ¶È:50% Shoyakugaku Zasshi 1991 45 255-260 Studies on the Chemical Constituents of Gloriosa rothschildiana and Colchicum autumnale MIMAKI YOSHIHIRO, ISHIBASHI NAOKO, KOMATSU MUTSUMI, SASHIDA YUTAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . compound 7d ÏàËÆ¶È:50% Chemical Journal of Chinese Universities 2013 34 2745-2751 Design, Synthesis and Activity Evaluation of N-Substituted Phthalimide Derivatives QIN Si-Ning, Lv Wen-Wen, WANG Quan, ZHAO Qing-Chun*, XU Yong-Nan, * Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2014-07-02 10:36:41













»Ø¸´´ËÂ¥
20