| ²é¿´: 1388 | »Ø¸´: 4 | ||
yaoxue1122½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
Çó²éÒ»¸ö»¯ºÏÎï΢Æ×Êý¾Ý
|
| »¯ºÏÎï̼Æ× 18.9,23.9,26.0,36.9,40.9,48.4,51.8,80.4,51.8,80.4,85.1,86.9,89.3,91.3,111.5,170.8 |
» ²ÂÄãϲ»¶
283Çóµ÷¼Á 086004¿¼Ó¢¶þÊý¶þ
ÒѾÓÐ4È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ35È˻ظ´
µ÷¼ÁÇóÊÕÁô
ÒѾÓÐ10È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó 085600 277 12²Ä¿Æ»ùÇóµ÷¼Á
ÒѾÓÐ18È˻ظ´
0831ÉúÒ½¹¤µÚÒ»ÂÖµ÷¼Áʧ°ÜÇóÖú
ÒѾÓÐ9È˻ظ´
ÉúÎïѧ308Çóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©
ÒѾÓÐ6È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ36È˻ظ´
275Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
Çó½âÈ·¶¨Ò»¸ö»¯ºÏÎïµÄÀàÐÍ£¬ÇâÆ×ºÍ·Ö×ÓÁ¿ÒÑÖª...ÏêϸÔÚÌùÖÐ
ÒѾÓÐ5È˻ظ´
¼±Çó΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÇëÇó´ó¼ÒÇóÑéÖ¤Ò»¸ö»¯ºÏÎ¸½ÉÏH1ºÍC13Æ×ͼ£¬Ïà¶Ô½Ï¼òµ¥µÄÒ»¸ö»ÆÍªÜÕÀ໯ºÏÎï¡£
ÒѾÓÐ4È˻ظ´
ÓÐûÓÐÒ»¸ö¿ÉÒÔ²éѯ»¯ºÏÎï±ê׼ͼÆ×µÄÍøÕ¾°¡£¿
ÒѾÓÐ4È˻ظ´
΢Æ×13C NMRÊý¾Ý¿â ²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
Ôõô²éÒ»¸öÒÑÖª½á¹¹»¯ºÏÎïµÄÈ۵㣿
ÒѾÓÐ9È˻ظ´
Çó¸ßÊÖÖ¸Õý¸Ã»¯ºÏÎï½á¹¹½âÎöÊÇ·ñÕýÈ·£¨¸½ÓÐÏêϸµÄ̼¡¢ÇâÆ×Êý¾Ý£©
ÒѾÓÐ7È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄÇâÆ×½âÎö
ÒѾÓÐ11È˻ظ´
ÇóÖú¹ØÓÚ»¯ºÏÎïÀí»¯ÐÔÖʲéѯµÄÍøÕ¾ºÍÊý¾Ý¿â
ÒѾÓÐ9È˻ظ´
ÇóÖú¡¡Î¢Æ×Êý¾Ý¿â £Ã£Î£Í£ÒÊý¾Ý²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
ÇëÎÊÓÐûÓÐÒ»¸ö»¯ºÏÎï±ê×¼Æ×ͼ½âÎöÊý¾Ý¿â£¿
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿¸÷λºÃ£¬ÇëÎÒ¿´Ò»¸ö¼òµ¥»¯ºÏÎïµÄHNMRÆ×ͼ¡£
ÒѾÓÐ20È˻ظ´
¡¾ÇóÖú¡¿ÈçºÎ²éµ½Ò»¸öÒÑÖª»¯ºÏÎïµÄ¾§Ìå½á¹¹Êý¾Ý£¿
ÒѾÓÐ7È˻ظ´
¡¾ÇóÖú¡¿ËÖªµÀÄÄÀï¿ÉÒԲ黯ºÏÎïµÄ̼Æ×°¡£¿
ÒѾÓÐ10È˻ظ´
¡¾Çë½Ì¡¿ÔõÑù²éѯһ¸ö»¯ºÏÎïµ¥¾§Êý¾Ýδ±»±¨µÀ£¿
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú²éSciFinder£¬Çë²éÕÒÒ»¸ö»¯ºÏÎïµÄºÏ³É·ÏߺͼìÑé·½·¨¡£Ð»Ð»£¡
ÒѾÓÐ8È˻ظ´
СÂü1211
ľ³æ (³õÈëÎÄ̳)
- Ó¦Öú: 17 (СѧÉú)
- ½ð±Ò: 1728.9
- ºì»¨: 1
- Ìû×Ó: 46
- ÔÚÏß: 25.3Сʱ
- ³æºÅ: 1533524
- ×¢²á: 2011-12-12
- רҵ: ÖÐÒ©×ÊÔ´
2Â¥2012-04-15 09:15:01
СÂü1211
ľ³æ (³õÈëÎÄ̳)
- Ó¦Öú: 17 (СѧÉú)
- ½ð±Ò: 1728.9
- ºì»¨: 1
- Ìû×Ó: 46
- ÔÚÏß: 25.3Сʱ
- ³æºÅ: 1533524
- ×¢²á: 2011-12-12
- רҵ: ÖÐÒ©×ÊÔ´
3Â¥2012-04-15 09:19:05
yaoxue1122
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 625.4
- É¢½ð: 80
- ºì»¨: 4
- Ìû×Ó: 162
- ÔÚÏß: 44.6Сʱ
- ³æºÅ: 1368226
- ×¢²á: 2011-08-14
- רҵ: Ò©Îﻯѧ
4Â¥2012-04-15 09:25:02
СÂü1211
ľ³æ (³õÈëÎÄ̳)
- Ó¦Öú: 17 (СѧÉú)
- ½ð±Ò: 1728.9
- ºì»¨: 1
- Ìû×Ó: 46
- ÔÚÏß: 25.3Сʱ
- ³æºÅ: 1533524
- ×¢²á: 2011-12-12
- רҵ: ÖÐÒ©×ÊÔ´
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yaoxue1122: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл°¡~~~~ 2012-04-15 13:35:54
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yaoxue1122: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл°¡~~~~ 2012-04-15 13:35:54
|
²éѯ½á¹û£º¹²²éµ½26¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound 4a ÏàËÆ¶È:57.1% Tetrahedron Letters 2004 45 7255-7259 Access to enantiopure polycyclic ¦Â-lactams by Diels-Alder reaction of novel inner-outer-ring 2-(silyloxy)dienes with a carbacepham skeleton Benito Alcaide, Rosa M. de Murga, Carmen Pardo, Carolina Rodr¨ªguez-Ranera Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . merrilliortholactone C15H24O7 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2002 50(1) 133-136 Brine Shrimp Lethality Test Active Constituents and New Highly Oxygenated Seco-prezizaane-Type Sesquiterpenes from Illicium merrillianum Jian-Mei HUANG,Kousuke NAKADE, Mamiko KONDO,Chun-Shu YANG,and Yoshiyasu FUKUYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 5¦Á-acetoxy-1¦Â,8¦Á-bis-cinnamoyl-4¦Á-hydroxydihydroagarofuran C35H40O8 ÏàËÆ¶È:53.3% Phytochemistry 2002 61 93-98 Terpenoids from Tripterygium doianum (Celastraceae) Naonobu Tanaka, Hongquan Duan, Yoshihisa Takaishi,Kazuyoshi Kawazoe, Satoru Goto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 7 C31H35O8N ÏàËÆ¶È:53.3% Phytochemistry 1997 45 617-621 Sesquiterpene alkaloids from Tripterygium hypoglaucum Hongquan Duan, Kazuyoshi Kawazoe, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 1¦Á-benzoyloxy-6¦Â,9¦Â-diacetoxy-4¦Â-hydroxydihydro-¦Â-agarofuran C26H34O8 ÏàËÆ¶È:53.3% Phytochemistry 1988 27 473-477 Sesquiterpenes from Orthosphenia mexicana Antonio G. Gonzalez,Carmen M. Gonza´lez,Angel G. Ravelo,Braulio M. Frag,Xorge A. Dominguez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Compound 5 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry Letters 2009 19 382-385 Synthesis of 10-substituted triazolyl artemisinins possessing anticancer activity via Huisgen 1,3-dipolar cylcoaddition Sungsik Cho, Sangtae Oh, Yumi Um, Ji-Hee Jung, Jungyeob Ham, Woon-Seob Shin, Seokjoon Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Compound 3 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry Letters 1994 4 751-752 Synthesis of a novel ring contracted artemisinin derivative. B. Venugopalan, C.P. Bapat, P.J. Karnik Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (1S,4R,5S,8R,9S,11S,12S)-1,5,9-Trimethyl-10,13,14,15-tetraoxatetracyclo[9.3.1.04,12.08,12]pentadecane-9a-carbaldehyde C15H22O5 ÏàËÆ¶È:53.3% Tetrahedron Letters 2001 42 2125-2127 Ring-contracted artemisinin derivatives: stereoselective reaction of anhydrodihydroartemisinin towards halogenating reagents Fabienne Grellepois, Dani¨¨le Bonnet-Delpon, Jean-Pierre B¨¦gu¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 13a ÏàËÆ¶È:52.9% Tetrahedron Letters 2002 43 7837-7840 Allylic bromination of anhydrodihydroartemisinin and of its 10-trifluoromethyl analogue: a new access to 16-substituted artemisinin derivatives Fabienne Grellepois, Fatima Chorki, Mich¨¨le Our¨¦vitch, Benoit Crousse, Dani¨¨le Bonnet-Delpon, Jean-Pierre B¨¦gu¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3¦Â-tetrahydro-O-acetyl-isophotosantonic lactone C17H26O5 ÏàËÆ¶È:52.9% Tetrahedron 2001 57 1297-1300 Configurations of alcohols obtained from dihydro-O-acetylisophoto-¦Á-santonic lactone B Garcı́a Marrero Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 4a ÏàËÆ¶È:50% Phytochemistry 2004 65 491-496 Fascicularones A and B from a mycelial culture of Naematoloma fasciculare Yoshihito Shiono, Ryutarou Matsuzaka, Hiroko Wakamatsu, Kimiko Muneta,Tetsuya Murayama, Michimasa Ikeda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . russujaponol A C15H24O4 ÏàËÆ¶È:50% Journal of Natural Products 2006 69 1267-1270 Russujaponols A−F, Illudoid Sesquiterpenes from the Fruiting Body of Russula japonica Kazuko Yoshikawa, Azusa Kaneko, Yuki Matsumoto, Hiroshi Hama, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (1S,4R,5S,8R,9S,11S,12S)-1,5,9-trimethyl-10,13,14,15-tetraoxatetracyclo[9.1.3.1.04,12.08,12]pentadecyl-9¦Á-2'-aminoacetonitrile ÏàËÆ¶È:50% Molecules 2007 12 395-405 Functionalisation of Artemisinin and Its Ring-contracted Derivatives Tine Van Neck, Sarah Van Mierloo and Wim Dehaen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (1S,4R,5S,8R,9S,11S,12S)-1,5,9-trimethyl-10,13,14,15-tetraoxatetracyclo[9.1.3.1.0(4),1(2).0(8),1(2)]pentadecyl-9¦Á-2'-hydroxyacetonitrile ÏàËÆ¶È:50% Molecules 2007 12 395-405 Functionalisation of Artemisinin and Its Ring-contracted Derivatives Tine Van Neck, Sarah Van Mierloo and Wim Dehaen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . ent-4¦Â-Hydroxy-10¦Á-methoxyaromadendrane ÏàËÆ¶È:50% Phytochemistry 2000 53 845-849 Sesquiterpenoids and diterpenoids from the Chilean liverwort Lepicolea ochroleuca Huei-Ju Liu, Chia-Li Wu, Hans Becker, Josef Zapp Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 8¦Â-hydroxy phlegmariurine B C16H23NO3 ÏàËÆ¶È:50% Acta Pharmaceutica Sinica 2003 Vol 38 596-598 A novel phlegmariurine type alkaloid from Huperzia serrata (Thunb.)Trev YUAN Shan qin; ZHAO Yi min Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 5¦Î-methoxycarbonyl-3,3,5-trimethyl-2-[2',3'-O-isopropyliden-¦Â-D-ribofuranosyl]-isoxazolidin C16H27NO7 ÏàËÆ¶È:50% Helvetica Chimica Acta 1977 60 426-446 Synthese und Umwandlungen von Isoxazolidin-Nucleosiden Andrea Vasella Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . Kiagiside aglucone acetyl derivative C13H16O7 ÏàËÆ¶È:50% Phytochemistry 1985 24 771-772 Kingiside aglucone, a natural secoiridoid from unripe fruits of strychnos spinosa J. D. Msonthi, C. Galeffi, M. Nicoletti, I. Messana, G. B. Marini-Bettolo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . Kansuenin B ÏàËÆ¶È:50% Archives of Pharmacal Research 2007 30 431-435 A new iridoid and other chemical constituents from pedicularis kansuensis forma albiflora Li. Jun-Gang Yin, Cheng-Shan Yuan and Zhong-Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . compound 3g C14H21NO4 ÏàËÆ¶È:50% Tetrahedron Letters 2001 42 6995-6997 Diastereoselection of the addition of silyloxyfurans to five-, six- and seven-membered N-acyliminium ions Maria da Conceição F de Oliveira, Leonardo Silva Santos, Ronaldo Aloise Pilli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 5',9-anhydro-2',3'-O-isopropylidene-iso xanthosine C13H14N4O5 ÏàËÆ¶È:50% Tetrahedron Letters 2005 46 2825-2827 Synthesis of 5',9-anhydro-3-(¦Â-d-ribofuranosyl)xanthine, and 3,5'-anhydro-xanthosine as potential anti-hepatitis C virus agents Byoung-Kwon Chun, Peiyuan Wang, Abdalla Hassan, Jinfa Du, Phillip M. Tharnish, Lieven J. Stuyver, Michael J. Otto, Raymond F. Schinazi, Kyoichi A. Watanabe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 9-methylene-4¦Á-tert-butyldimethylsilyloxy-6,8-dimethyl-2,7-dioxatricyclo[4.2.1.0(3,8)nonane ÏàËÆ¶È:50% Tetrahedron 2002 58 6199-6206 Synthesis and studies of marine natural products: the dictyoxetane core from 8-oxabicyclo[3.2.1]oct-6-en-3-ones S Proemmel, R Wartchow, H.M.R Hoffmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . (-)-10¦Á-acetoxy-4¦Â-hydroxy-1¦ÁH,5¦ÂH-guaia-6-ene C15H26O2 ÏàËÆ¶È:50% The Journal of Organic Chemistry 2006 71 7866-7869 Syntheses of (+)-Alismoxide and (+)-4-epi-Alismoxide Gonzalo Blay, Begoña Garc¨ªa, Eva Molina, and Jos¨¦ R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . compound 23 C16H22O5 ÏàËÆ¶È:50% Tetrahedron 2000 56 6331-6338 Synthesis of 3-Oxa-guaianolides from Santonin Gonzalo Blay, Luz Cardona, Begoña Garcı́a, Luisa Lahoz, Bel¨¦n Monje, Jos¨¦ R Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 9-methanesulfonyl-DHA C16H26O7S ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 5247-5253 Electronically stabilized versions of the antimalarial acetal trioxanes artemether and artesunate Gary H. Posner, William A. Maio, Alvin S. Kalinda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . 4,6,6-trimethylspiro[bicyclo[3.1.1]hept-3-ene-2,2'-[1,3]dithiolane] 1'-oxide ÏàËÆ¶È:50% Russian Journal of Organic Chemistry 2009 45 581-586 Asymmetric oxidation of verbenone ethylene dithioacetal A. V. Timshina, S. A. Rubtsova, L. L. Frolova, I. N. Alekseev and P. A. Slepukhin, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |
5Â¥2012-04-15 11:55:19













»Ø¸´´ËÂ¥
10