| ²é¿´: 351 | »Ø¸´: 1 | |||
badhuster½ð³æ (ÕýʽдÊÖ)
ѧǰ°à°à³¤
|
[ÇóÖú]
±ÏÒµÔÚ¼´¡£Î¢Æ×ÇóÖú¡£¡£Ð»Ð»´ó¼Ò£¡ ÒÑÓÐ1È˲ÎÓë
|
|
(xjc-44) 13C NMR (CDCl3, 101 MHz) ¦Ä 15.93, 20.63, 55.83, 62.68, 63.88, 74.29, 80.31, 101.23, 108.17, 108.34, 110.25, 118.64, 119.66, 121.38, 127.44, 127.53, 127.55, 130.43, 131.07, 132.05, 139.08, 139.49, 147.43, 147.71, 147.87, 151.07, 166.47, 167.66. |
» ²ÂÄãϲ»¶
һ־Ը³¶«´óѧ071000ÉúÎïѧѧ˶³õÊÔ·ÖÊý276Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó 085600 277 12²Ä¿Æ»ùÇóµ÷¼Á
ÒѾÓÐ33È˻ظ´
Ò»Ö¾Ô¸Öйú¿ÆÑ§ÔºÉϺ£ÓлúËù£¬Óлú»¯Ñ§356·ÖÕÒµ÷¼Á
ÒѾÓÐ12È˻ظ´
071000ÉúÎïѧ£¬Ò»Ö¾Ô¸ÉîÛÚ´óѧ296·Ö£¬Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
0854µ÷¼Á
ÒѾÓÐ12È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ37È˻ظ´
271Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
²ÄÁÏÏà¹Ø×¨Òµ344Çóµ÷¼ÁË«·Ç¹¤¿ÆÑ§Ð£»ò¿ÎÌâ×é
ÒѾÓÐ11È˻ظ´
»¯¹¤Ñ§Ë¶294·Ö£¬Çóµ¼Ê¦ÊÕÁô
ÒѾÓÐ14È˻ظ´
2026 WRÇà°Î
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»°ïÖú¡£
ÒѾÓÐ3È˻ظ´
ÇóÖú3¸ö΢Æ×£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл¸÷λ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл´ó¼Ò
ÒѾÓÐ3È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¼±£¡Ð»Ð»£¡
ÒѾÓÐ5È˻ظ´
European Journal of Wood and Wood Products
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
Óнð±Ò£¬½ô¼±ÇóÖú£¡£¡springer ÆìÏÂÆÚ¿¯ my publication ÇóÖú£¬Ð»Ð»´ó¼Ò£¡£¡
ÒѾÓÐ10È˻ظ´
΢Æ×Ò»¸ö£¬ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»df12
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
СµÜÃ÷ÌìÔçÉϱÏÒµ´ð±ç£¬ÇóÖúϺìÍ⣬лл
ÒѾÓÐ6È˻ظ´
Ͷ·ÖÎö¿ÆÑ§Ñ§±¨ÇóÖú£¬¼±¼±¼±£¡£¡£¡Ð»Ð»´ó¼ÒÁË
ÒѾÓÐ4È˻ظ´
RUSSIAN CHEMICAL BULLETIN
ÒѾÓÐ5È˻ظ´

seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48433.9
- ºì»¨: 52
- Ìû×Ó: 6749
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
badhuster: ½ð±Ò+10 2015-04-08 21:50:50
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
badhuster: ½ð±Ò+10 2015-04-08 21:50:50
|
1 . ethyl 4-[1-(1,3-benzodioxol-5-yl)-9H-¦Â-carbolin-3-yl]-2-oxo-6-phenyl-1,2,3,4-tetrahydropyrimidine-5-carboxylate C31H24N4O5 ÏàËÆ¶È:58.6% Tetrahedron 2014 70 5711-5719 Convenient synthesis of 1-aryl-9H-¦Â-carboline-3-carbaldehydes and their transformation into dihydropyrimidinone derivatives by Biginelli reaction P¨¦ter ¨¢br¨¢nyi-Balogh, Andr¨¢s Dancs¨®, D¨¢vid Frigyes, Bal¨¢zs Volk, György Keglevich, M¨¢ty¨¢s Milen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . rhaponticin 6''-O-gallate C28H28O13 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 1984 32 3501-3517 Studies on Rhubarb (Rhei Rhizoma). VI. Isolation and Characterization of Stilbenes YOSHIKI KASHIWADA,GENICHIRO NONAKA and ITSUO NISHIOKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . guaiacylglycerol-¦Â-O-6'-(2-rnethoxy)cinnamyl alcohol ether tetraacetate ÏàËÆ¶È:57.1% Phytochemistry 1996 43 409-412 A lignan and four terpenoids from Brucea javanica that induce differentiation with cultured HL-60 promyelocytic leukemia cells Lumonadio Luyengi, Nanjoo Suh, Harry H. S. Fong, John M. Pezzuto, A. Douglas Kinghorn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . cis-N-[9,10-dimethoxy-2-(3'',4''-methylenedioxyphenyl)-4-oxo-1-phenyl-3,4,6,7-tetrahydro-2H-pyrido[2,1-a]isoquinolin-3-yl]acetamide C30H28N2O6 ÏàËÆ¶È:57.1% Tetrahedron 2012 68 2864-2875 Synthesis of benzoindoloquinolizines via a Cu(I)-mediated C¨CN bond formation Rattana Worayuthakarn, Prattya Nealmongkol, Somsak Ruchirawat, Nopporn Thasana Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . trans-N-[9,10-dimethoxy-2-(3'',4''-methylenedioxyphenyl)-4-oxo-1-phenyl-3,4,6,7-tetrahydro-2H-pyrido[2,1-a]isoquinolin-3-yl]acetamide C30H28N2O6 ÏàËÆ¶È:57.1% Tetrahedron 2012 68 2864-2875 Synthesis of benzoindoloquinolizines via a Cu(I)-mediated C¨CN bond formation Rattana Worayuthakarn, Prattya Nealmongkol, Somsak Ruchirawat, Nopporn Thasana Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (2R,3R,3aR,11aR)-10-[(1,3-benzodioxol-5-yl)methyl]-2,3-(isopropylidenedioxy)-4-(p-tolylsulfonyl)-3a,4,5,10,11,11a-hexahydrofuro[3,2-b][1,5]benzodiazocine C30H32N2O7S ÏàËÆ¶È:57.1% European Journal of Organic Chemistry 2010 1754-1762 Palladium-Catalyzed Intramolecular Aryl Amination Reaction: An Expeditious Approach to the Synthesis of Chiral Benzodiazocine Derivatives Nirmal Das Adhikary and Partha Chattopadhyay Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ethyl 4-[1-(1,3-benzodioxol-5-yl)-9H-¦Â-carbolin-3-yl]-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate C26H22N4O5 ÏàËÆ¶È:57.1% Tetrahedron 2014 70 5711-5719 Convenient synthesis of 1-aryl-9H-¦Â-carboline-3-carbaldehydes and their transformation into dihydropyrimidinone derivatives by Biginelli reaction P¨¦ter ¨¢br¨¢nyi-Balogh, Andr¨¢s Dancs¨®, D¨¢vid Frigyes, Bal¨¢zs Volk, György Keglevich, M¨¢ty¨¢s Milen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . methyl 4-[1-(1,3-benzodioxol-5-yl)-9H-¦Â-carbolin-3-yl]-6-(1-methylethyl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate C27H24N4O5 ÏàËÆ¶È:57.1% Tetrahedron 2014 70 5711-5719 Convenient synthesis of 1-aryl-9H-¦Â-carboline-3-carbaldehydes and their transformation into dihydropyrimidinone derivatives by Biginelli reaction P¨¦ter ¨¢br¨¢nyi-Balogh, Andr¨¢s Dancs¨®, D¨¢vid Frigyes, Bal¨¢zs Volk, György Keglevich, M¨¢ty¨¢s Milen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . trans-N-[2-(3'',4''-dimethoxyphenyl)-9,10-dimethoxy-4-oxo-1-phenyl-3,4,6,7-tetrahydro-2H-pyrido[2,1-a]isoquinolin-3-yl]benzamide C36H34N2O6 ÏàËÆ¶È:55.1% Tetrahedron 2012 68 2864-2875 Synthesis of benzoindoloquinolizines via a Cu(I)-mediated C¨CN bond formation Rattana Worayuthakarn, Prattya Nealmongkol, Somsak Ruchirawat, Nopporn Thasana Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . phyllamyricin E C22H18O7 ÏàËÆ¶È:53.5% Journal of Natural Products 1996 59 1061-1065 Six Lignans from Phyllanthus myrtifolius Shoei-Sheng Lee, Mei-Tsu Lin, Chao-Lin Liu, Yung-Yaw Lin, and Karin C. S. Chen Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 1a C31H26O11 ÏàËÆ¶È:53.5% Chemical & Pharmaceutical Bulletin 1991 39 1466-1472 Studies on Nepalese Crude Drugs. XIV. New Flavonoids from the Root of Scutellaria prostrata JACQ. ex BENTH. Yuichi KIKUCHI,Yukinori MIYAICHI and Tsuyoshi TOMIMORI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . mananthoside A C27H26O11 ÏàËÆ¶È:53.5% Chinese Chemical Letters 2002 13 959-962 Two New Arylnaphthalene Lignan Glycosides from Mananthes patentiflora Bin CHEN, Yan LIU, Chun FENG, Bo Gang LI, Guo Lin ZHANG Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . mono-O-acetyldaurinol glucoside ÏàËÆ¶È:53.5% Phytochemistry 1990 29 2659-2661 Two arylnaphthalene lignans from Haplophyllum buxbaumii Yousef Al-Abed,Salim Sabri,Musa Abu Zarga,Zahir Shah,Atta-Ur-Rahman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (E)-3(5)-[¦Â-(4-hydroxy-3-methoxyphenyl)-ethenyl]-5(3)-phenyl-1H-pyrazole C18H16N2O2 ÏàËÆ¶È:53.5% Bioorganic & Medicinal Chemistry 2009 17 1290-1296 Synthesis and biological evaluation of curcuminoid pyrazoles as new therapeutic agents in inflammatory bowel disease: Effect on matrix metalloproteinases R.M. Claramunt, L. Bouissane, M.P. Cabildo, M.P. Cornago, J. Elguero, A. Radziwon, C. Medina Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 11b C30H28N2O6 ÏàËÆ¶È:53.5% Tetrahedron 2012 68 2864-2875 Synthesis of benzoindoloquinolizines via a Cu(I)-mediated C¨CN bond formation Rattana Worayuthakarn, Prattya Nealmongkol, Somsak Ruchirawat, Nopporn Thasana Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 11e C28H23BrN2O4 ÏàËÆ¶È:53.5% Tetrahedron 2012 68 2864-2875 Synthesis of benzoindoloquinolizines via a Cu(I)-mediated C¨CN bond formation Rattana Worayuthakarn, Prattya Nealmongkol, Somsak Ruchirawat, Nopporn Thasana Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-12 10:13:23













»Ø¸´´ËÂ¥