| ²é¿´: 580 | »Ø¸´: 3 | ||||
·½Ð¡Æ½½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¨307-75a£© ÒÑÓÐ1È˲ÎÓë
|
|
13C NMR (126 MHz, MeOD) ¦Ä 30.31,61.34, 110.87, 141.16,170.60, 176.68. ÏàËÆ¶ÈÒªÇó>60% ÈܼÁ£ºë®´ú¼×´¼ лл£¡ |
» ²ÂÄãϲ»¶
085700×ÊÔ´Óë»·¾³308Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
265Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
279·ÖÇóµ÷¼Á Ò»Ö¾Ô¸211
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸¼ªÁÖ´óѧ²ÄÁÏѧ˶321Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
286·ÖÈ˹¤ÖÇÄÜרҵÇëÇóµ÷¼ÁÔ¸Òâ¿ç¿¼£¡
ÒѾÓÐ3È˻ظ´
329Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
ÉêÇë»Ø¸åÑÓÆÚÒ»¸öÔ£¬±à¼Í¬ÒâÁË¡£µ«ÏµÍ³ÉϵÄʱ¼äû±ä£¬¸ø±à¼ÓÖдÓʼþÁË£¬Ã»»Ø¸´
ÒѾÓÐ4È˻ظ´
²ÄÁÏѧ˶318Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸Öйúº£Ñó´óѧ£¬ÉúÎïѧ£¬301·Ö£¬Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú¡¢¡¢¡¢Ð»Ð»´óÉñ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¼±£¡Ð»Ð»£¡
ÒѾÓÐ5È˻ظ´
ÇóÖúÌìȻҩÎﻯѧÌáÈ¡·ÖÀëÒ»¸ö»¯ºÏÎïµÄ΢Æ×
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú3¸ö΢ÆÕÊý¾Ý
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
΢Æ×Êý¾Ý¡£Ç󻯺ÏÎï½âÎö
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÈË΢Æ×²éѯ£¬¼±£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
·½Ð¡Æ½: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-09-04 19:35:01
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
·½Ð¡Æ½: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-09-04 19:35:01
|
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 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½35¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 5-hydroxymethylfuran-3-carboxylic acid C6H6O4 ÏàËÆ¶È:83.3% Phytochemistry 2002 61 25-30 Identification of the major glucosinolate (4-mercaptobutyl glucosinolate) in leaves of Eruca sativa L. (salad rocket) Richard N. Bennett, Fred A. Mellon, Nigel P. Botting, John Eagles,Eduardo A.S. Rosa, Gary Williamson Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Flufuran C6H6O4 ÏàËÆ¶È:83.3% Chemistry & Biodiversity 2009 6 328-334 Flufuran, an Antifungal 3,5-Disubstituted Furan Produced by Aspergillus flavus Link Antonio Evidente, Gennaro Cristinzio, Biancavaleria Punzo, Anna Andolfi, Antonino Testa, and Dominique Melck Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2-hydroxymethyl-5-hydroxy-¦Ã-pyrone ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2010 41 1787-1790 ëËὬËÞÝàµÄ»¯Ñ§³É·ÖÑо¿ ÕÅ»Ô;³ÂÖØ;ÀîÏÄ;ÀîЦȻ;ÐíÇíÃ÷;ÑîÊÀÁÖ Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Methyl 5-(Hydroxymethyl)furan-3-carboxylate ÏàËÆ¶È:71.4% Chemistry & Biodiversity 2009 6 328-334 Flufuran, an Antifungal 3,5-Disubstituted Furan Produced by Aspergillus flavus Link Antonio Evidente, Gennaro Cristinzio, Biancavaleria Punzo, Anna Andolfi, Antonino Testa, and Dominique Melck Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . bergenin C8H8O5 ÏàËÆ¶È:66.6% Phytochemistry 1989 28 1289-1290 A bacterial cleavage of the C-glucosyl bond of mangiferin and bergenin Masao Hattori,Yue-Zhong Shu,Tsuyoshi Tomimori,Kyoichi Kobashi,Tsuneo Namba Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . gallic acid ÏàËÆ¶È:50% Helvetica Chimica Acta 2004 Vol. 87 758 Chemical Constituents from the Pericarp of Trewia nudiflora Zhi-Zhi Du, Hong-Ping He, Bin Wu, Yue-Mao Shen, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . trans-3-methylsulfonyl-2-propenol(1a) C6H11O4S ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2003 51(12) 1423-1425 Sulfur-Containing Compounds from Clinacanthus siamensis Pittaya TUNTIWACHWUTTIKUL,Yupa POOTAENG-ON,a Pootchana PANSA, Thongchai SRISANPANG,and Walter Charles TAYLOR Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ÇúËá C5H8N2O2 ÏàËÆ¶È:50% Chinese Journal of Marine Drugs 2005 24(2) 9-12 Studies on the chemical constituents of the fermentation liquid from marine bacterium Bacillus sp. ZHANG Hai-long, FU Hong-wei, TIAN Li, HUA Hui-ming, PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (S)-¦Á-Methylaspartic Acid C5H9NO4 ÏàËÆ¶È:50% The Journal of Organic Chemistry 2011 76 1621-1633 Asymmetric Synthesis of r-Methyl-r-Amino Acids via Diastereoselective Alkylation of (1S)-(+)-3-Carene Derived Tricyclic Iminolactone Ta-Jung Lu and Cheng-Kun Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3,3'-(4-Hydroxypyridine-2,6-diyl)dipropanoic Acid Hydrochloride C11H14ClNO5 ÏàËÆ¶È:50% Helvetica Chimica Acta 2012 95 197-210 Trinuclear Non-Heme Iron Complexes Based on 4-Substituted 2,6-Diacylpyridine Ligands as Catalysts in Aerobic Allylic Oxidations Volker Rabe, Wolfgang Frey, Angelika Baro, and Sabine Laschat Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . dimethyl 2-cyanomalonate(enol-form) C6H7NO4 ÏàËÆ¶È:50% Heterocycles 2003 59 161-167 3-Cyano-2-(N-cyanoimino)thiazolidine (3-cyano-NCT): An Efficient Electrophilic Cyanating Agent for Activated Methylene Compounds Naoyoshi Maezaki, Akemi Furusawa, Shuji Uchida, and Tetsuaki Tanaka* Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . N-[¦Á-Ethylbenzyl]-N'-[2-(thiazo-lyl)]thiourea ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2001 11 523-528 Anti-HIV activity of aromatic and heterocyclic Thiazolyl Thiourea compounds T. K. Venkatachalam, Elise A. Sudbeck, Chen Mao, Fatih M. Uckun Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 4-Azido-5-hydroxypipecolate C6H10N4O3 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 1998 8 739-744 Epoxide derivatives of pipecolic acid and proline are inhibitors of pipecolate oxidase Bin Ho, T. Mark Zabriskie Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 4u ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 3203-3207 Chemical versus enzymatic acetylation of ¦Á-bromo-¦Ø-hydroxyaldehydes: decyclization of hemiacetals by lipase Ly Villo, Andrus Metsala, Omar Parve, Tõnis Pehk Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 5a ÏàËÆ¶È:50% Tetrahedron Letters 2003 44 3101-3104 The tricyclo[2.1.0.02,5]pentan-3-one system: a new probe for the study of ¦Ð-facial selectivity in nucleophilic additions Goverdhan Mehta, S.Robindro Singh, U.Deva Priyakumar, G.Narahari Sastry Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 5 C14H22N2O3 ÏàËÆ¶È:50% Tetrahedron Letters 2003 44 9213-9217 Synthesis of new conformationally rigid paramagnetic ¦Á-amino acids M¨¢ria Balog, Tam¨¢s K¨¢lai, J¨®zsef Jekő, Zolt¨¢n Berente, Heinz-J¨¹rgen Steinhoff, Martin Engelhard, K¨¢lm¨¢n Hideg Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-09-04 18:35:35
·½Ð¡Æ½
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 2407.1
- ºì»¨: 1
- Ìû×Ó: 149
- ÔÚÏß: 54Сʱ
- ³æºÅ: 2474109
- ×¢²á: 2013-05-21
- ÐÔ±ð: GG
- רҵ: ϸ°ûÉú³¤Óë·ÖÁÑ
3Â¥2014-09-04 19:05:31
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ

4Â¥2014-09-04 19:23:29













»Ø¸´´ËÂ¥