Znn3bq.jpeg
±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 172  |  »Ø¸´: 1

jlh84466939

½ð³æ (³õÈëÎÄ̳)

[ÇóÖú] ÇóһάÆÕÊý¾Ý

13C NMR (126 MHz, CDCl3) ¦Ä 191.0, 151.8, 147.2, 145.0, 144.6, 143.6, 132.4, 131.9, 129.9, 129.9, 127.6, 116.6, 115.9, 115.2, 115.0, 114.7, 114.4, 109.5, 108.9, 56.1, 56.0, 51.6
ÓÉÓÚÆäÖÐÓÐÔÓÖÊ£¬¿ÉÄÜÎó°ÑÔÓÖÊ·åËãÈ룬¹Ê¸½ÉϺ˴ÅÔ­Æ×£¬Çë´óÏÀÖ¸½Ì¡£Ð»Ð»¡£
»Ø¸´´ËÂ¥

» ±¾Ìû¸½¼þ×ÊÔ´Áбí

  • »¶Ó­¼à¶½ºÍ·´À¡£ºÐ¡Ä¾³æ½öÌṩ½»Á÷ƽ̨£¬²»¶Ô¸ÃÄÚÈݸºÔð¡£
    ±¾ÄÚÈÝÓÉÓû§×ÔÖ÷·¢²¼£¬Èç¹ûÆäÄÚÈÝÉæ¼°µ½ÖªÊ¶²úȨÎÊÌ⣬ÆäÔðÈÎÔÚÓÚÓû§±¾ÈË£¬Èç¶Ô°æÈ¨ÓÐÒìÒ飬ÇëÁªÏµÓÊÏ䣺xiaomuchong@tal.com
  • ¸½¼þ 1 : Document1.mnova
  • 2013-05-02 22:46:38, 417.78 K

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

ÈËÉúûÓÐÍêÃÀ£¬Ö»Ðè×öµ½ÎÊÐÄÎÞÀ¢£¡
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

wm0629

Ìú¸Ëľ³æ (ÖøÃûдÊÖ)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
PSA: ½ð±Ò+1, лл 2013-05-03 08:47:54
jlh84466939: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-05-03 20:24:14
1 .     xylobuxin
C21H22O7     ÏàËÆ¶È:66.6%
Journal of Natural Products          1995          Vol 58          786-789
Isolation and Structure Elucidation of Xylobuxin, a New Neolignan from Xylopia buxifolia
Anne Wahl, François Roblot, Andr¨¦ Cav¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     imperanene
C19H22O5     ÏàËÆ¶È:61.9%
Journal of Natural Products          1995          Vol 58          138-139
Imperanene, a Novel Phenolic Compound with Platelet Aggregation Inhibitory Activity from Imperata cylindrica
Kimihiro Matsunaga, Masaoki Shibuya, Yasushi Ohizumi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Iryantheral
C18H20O6     ÏàËÆ¶È:57.1%
Biochemical Systematics and Ecology          2009          37          772-775
Chemical constituents from Iryanthera ulei Warb
Freddy Alexander Bernal, Luis Enrique Cuca Su¨¢rez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (E)-3'-hydroxy-4'-(1''-hydroxyethyl)-phenyl-4-methoxycinnamate
C18H18O5     ÏàËÆ¶È:57.1%
Natural Product Research          2007          21          736-741
New cinnamic acid esters from Ocimum basilicum
Bina S. Siddiqui; Huma Aslam; Sabira Begum; Syed Tariq Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     perseal A
C18H20O6     ÏàËÆ¶È:57.1%
Phytochemistry          1996          43          1261-1263
Cytotoxic neolignans from Persea obovatifolia
Ian-Lih Tsai, Chih-Feng Hsieh, Chang-Yih Duh, Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     perseal B
C18H20O6     ÏàËÆ¶È:57.1%
Phytochemistry          1996          43          1261-1263
Cytotoxic neolignans from Persea obovatifolia
Ian-Lih Tsai, Chih-Feng Hsieh, Chang-Yih Duh, Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 2j
C16H14O5NBr     ÏàËÆ¶È:57.1%
Canadian Journal of Chemistry          2008          86          142-145
Ring opening of , -epoxy phenyl ketones with ceric ammonium nitrate (CAN) and potassium bromide
Zhou Lu, Wentao Wu, Lijun Peng, and Longmin Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     verrucosin
    ÏàËÆ¶È:57.1%
Bioscience, Biotechnology, and Biochemistry          2007          71          1028-1035
Antifungal Activity of Tetra-Substituted Tetrahydrofuran Lignan, (−-Virgatusin, and Its Structure-Activity Relationship
Koichi AKIYAMA, Satoshi YAMAUCHI, Tomofumi NAKATO, Masafumi MARUYAMA, Takuya SUGAHARA and Taro KISHIDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     isoshonanin
    ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry          2009          17          5676-5682
A novel and efficient synthesis of highly oxidized lignans by a methyltrioxorhenium/hydrogen peroxide catalytic system. Studies on their apoptogenic and antioxidant activity
Roberta Bernini, Giampiero Gualandi, Claudia Crestini, Maurizio Barontini, Maria Cristina Belfiore, Stefan Willför, Patrik Eklund, Raffaele Saladino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     6-fluoro-2-(4-methoxyphenyl)-4-phenylquinoline
C22H16FNO     ÏàËÆ¶È:57.1%
Heterocycles          2012          85          639-649
Efficient Synthesis of 2,4-Diarylquinolines via Fe(III) Trifluoroacetate Catalyzed Three-Component Reactions under Solvent-Free Conditions
Min Zhang,* Ting Wang, Biao Xiong, Fengxia Yan, Xiaoting Wang, Yuqiang Ding, and Qijun Song
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     2-(3-methoxy-4-hydroxyphenyl)-7-methoxy-5-vinyl-2,3-dihydrobenzofuran
C18H18O4     ÏàËÆ¶È:57.1%
Tetrahedron          2013          69          653-657
Cerium ammonium nitrate-mediated the oxidative dimerization of p-alkenylphenols: a new synthesis of substituted (¡À)-trans-dihydrobenzofurans
Po-Yuan Chen, Yi-Hua Wu, Mon-Huei Hsu, Tzu-Pin Wang, Eng-Chi Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     1-(4-aminobenzyl)-6,7-dimethoxy-3,4-dihydroisoquinoline
C18H20N2O2     ÏàËÆ¶È:54.5%
Heterocycles          2006          68          369-374
One-Pot Synthesis of 1-(2-, 3- or 4-Aminophenyl)- and 1-(4-Aminobenzyl)-3,4-dihydroisoqunolines
Iliyan Ivanov,* Stoyanka Nikolova, and Stela Statkova-Abeghe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3,6-bis-(3-hydroxy-4-methoxyphenyl)-thieno[2,3-b]pyrrolizin-8-one
C23H17NO5S     ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry          2009          17          7783-7788
Synthesis, reactivity and biological evaluation of novel halogenated tripentones
Vittoria Perri, Christophe Rochais, Thierry Cresteil, Patrick Dallemagne, Sylvain Rault
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 18
C22H21O8     ÏàËÆ¶È:54.5%
Journal of the American Chemical Society          2009          131          1745-1752
Explorations into Neolignan Biosynthesis: Concise Total Syntheses of Helicterin B, Helisorin, and Helisterculin A from a Common Intermediate
Scott A. Snyder and Ferenc Kontes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     4-[5-(2-Allyl-3,4-dimethoxy-phenyl)-3-phenyl-pyrazol-1-yl]-benzaldehyde
C27H24N2O3     ÏàËÆ¶È:54.5%
Tetrahedron          2012          68          7941-7948
Synthesis of 1,3-diaryl-1H-benzo[g]indazoles
Meng-Yang Chang, Hang-Yi Tai, Yeh-Long Chen, Ru-Ting Hsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     isolicarinA
C20H22O4     ÏàËÆ¶È:52.3%
Helvetica Chimica Acta          2007          Vol. 90          1491
Three New Neolignans from the Aril of Myristica fragrans
Fei Li and Xiu-Wei Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     vitexdoin C
C19H16O5     ÏàËÆ¶È:52.3%
Journal of Natural Products          2009          72          1627-1630
Nitric Oxide Scavenging Lignans from Vitex negundo Seeds
Cheng-Jian Zheng, Bao-Kang Huang, Ting Han, Qiao-Yan Zhang,Hong Zhang, Khalid Rahman, and Lu-Ping Qin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     kadsuralignan C
C21H26O5     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          2006          54(7)          1022-1025
New Lignans from Kadsura coccinea and Their Nitric Oxide Inhibitory Activities
He-Ran LI,Yu-Lin FENG,Zhi-Gang YANG,Jue WANG,Akihiro DAIKONYA,Susumu KITANAKA,Li-Zhen XU,and Shi-Lin YANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     odoratisol B
C20H24O5     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          2006          54(3)          380-383
New Neolignans and Lignans from Vietnamese Medicinal Plant Machilus odoratissima NEES
PHAN Minh Giang,PHAN Tong Son,Katsuyoshi MATSUNAMI,and Hideaki OTSUKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     odoratisol C
C20H24O5     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          2006          54(3)          380-383
New Neolignans and Lignans from Vietnamese Medicinal Plant Machilus odoratissima NEES
PHAN Minh Giang,PHAN Tong Son,Katsuyoshi MATSUNAMI,and Hideaki OTSUKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (+)-pinoresinol
    ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          2004          52(10)          1265-1267
A New Lignan from Balanophora abbreviata and Inhibition of Lipopolysaccharide (LPS)-induced Inducible Nitric Oxide Synthase(iNOS) Expression
Akihiro HOSOKAWA,Megumi SUMINO, Tomonori NAKAMURA,Shingo YANO, Toshikazu SEKINE,Nijsiri RUANGRUNGSI, Kazuko WATANABE,and Fumio IKEGAMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     angeliferulate
C21H24O8     ÏàËÆ¶È:52.3%
Journal of Natural Products          2006          69(4)          536-541
Serotonergic Activity-Guided Phytochemical Investigation of the Roots of Angelica sinensis
Shixin Deng, Shao-Nong Chen, Ping Yao, Dejan Nikolic, Richard B. van Breemen, Judy L. Bolton, Harry H. S. Fong, Norman R. Farnsworth, and Guido F. Pauli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     prostephabyssine a
    ÏàËÆ¶È:52.3%
Journal of Natural Products          2005          68          1201-1207
Hasubanan Type Alkaloids from Stephania longa
Hua Zhang, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     (2aS,3S,8aR)-5-Hydroxy-3-(4-hydroxy-3-methoxyphenyl)-6-methoxy-2,2a,8,8a-tetrahydronaphthalene[2,3-c]tetrahydrofuran
C26H22O5     ÏàËÆ¶È:52.3%
Journal of Natural Products          2005          68          1459-1470
Effect of Benzylic Oxygen on the Antioxidant Activity of Phenolic Lignans
Satoshi Yamauchi, Yoshimasa Hayashi, Yuki Nakashima,Takuya Kirikihira, Kazuki Yamada, and Toshiya Masuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     3-methoxy-4-hydroxylonchocarpin
C22H24O4     ÏàËÆ¶È:52.3%
Journal of Natural Products          1999          62          205-210
New Bioactive Flavonoids and Stilbenes in Cub¨¦ Resin Insecticide
Nianbai Fang and John E. Casida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
¼èÄÑÀ§¿à£¬ÓñÈêÓڳɡ£
2Â¥2013-05-03 07:46:51
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ jlh84466939 µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 273Çóµ÷¼Á +40 ÂóС¶£µ± 2026-04-06 47/2350 2026-04-08 13:02 by grayjzr
[¿¼ÑÐ] 297Çóµ÷¼Á +16 GENJIOW 2026-04-07 17/850 2026-04-08 11:05 by ÄæË®³Ë·ç
[¿¼ÑÐ] 368»¯Ñ§Çóµ÷¼Á +4 wwwwabcde 2026-04-07 5/250 2026-04-07 22:51 by wwwwabcde
[¿¼ÑÐ] 259Çóµ÷¼Á +5 ¾Í°®³ÔÍÁ¶¹Ñ½Ñ½ 2026-04-07 5/250 2026-04-07 22:40 by JourneyLucky
[¿¼ÑÐ] 326Çóµ÷¼Á +5 9ahye 2026-04-02 6/300 2026-04-07 21:37 by lijunpoly
[¿¼ÑÐ] 305Çóµ÷¼Á +4 77Qi 2026-04-06 4/200 2026-04-07 20:06 by shanqishi
[¿¼ÑÐ] ÐŹ¤Ëù11408 340·Ö ±¾¿ÆÎ÷°²½»´ó×Ô¶¯»¯ +3 moontrek 2026-04-06 3/150 2026-04-07 09:56 by chongya
[¿¼ÑÐ] ²ÄÁÏÓ뻯¹¤363ÇóÍÆ¼ö +11 zh096 2026-04-04 11/550 2026-04-06 19:14 by guanxin1001
[¿¼ÑÐ] ÇóÖú +3 ¿¨¿¨¶«88 2026-04-06 4/200 2026-04-06 15:28 by going home
[¿¼ÑÐ] Çóµ÷¼Á +5 wos666 2026-04-03 5/250 2026-04-06 10:13 by À¶ÔÆË¼Óê
[¿¼ÑÐ] Çóµ÷¼Á +7 ÕÅ.1 2026-04-05 7/350 2026-04-05 20:40 by à£à£à£0119
[¿¼ÑÐ] 327Çóµ÷¼Á +4 ʰ¹âÈÎȾ 2026-04-05 4/200 2026-04-05 20:16 by ÄϺ½~ÍòÀÏʦ
[¿¼ÑÐ] µ÷¼Á +3 ºÃºÃ¶ÁÊé¡£ 2026-04-02 3/150 2026-04-05 13:02 by arrow8852
[¿¼ÑÐ] µç×ÓÐÅÏ¢µ÷¼Á½»²æÑ§¿ÆÓÐÍÆ¼öÂð +6 jhtfeybgj 2026-04-01 9/450 2026-04-05 11:13 by Öí»á·É
[¿¼ÑÐ] 353Çóµ÷¼Á +10 MayUxw1 2026-04-03 10/500 2026-04-05 09:23 by Î޼ʵIJÝÔ­
[¿¼ÑÐ] 323Çóµ÷¼Á +8 Àî¼ÑÀÖ1 2026-04-04 8/400 2026-04-04 22:26 by hemengdong
[¿¼ÑÐ] ¿¼Ñе÷¼Á +5 ËÄ´¨ÍõÌÎ 2026-04-04 5/250 2026-04-04 22:18 by à£à£à£0119
[¿¼ÑÐ] ÊýÒ»Ó¢Ò»285Çóµ÷¼Á +7 AZMK 2026-04-03 9/450 2026-04-03 13:03 by ms629
[¿¼ÑÐ] 320Çóµ÷¼Á +3 ũҵ¹¤³ÌÓëÐÅÏ¢¼ 2026-04-03 3/150 2026-04-03 11:40 by ÍÁľ˶ʿÕÐÉú
[¿¼ÑÐ] Ò»Ö¾Ô¸±±¾©¿Æ¼¼²ÄÁÏ¿ÆÑ§Ó빤³Ì288·Ö£¬Çóµ÷¼Á +14 Êdz½°¡ 2026-04-02 14/700 2026-04-02 21:10 by dongzh2009
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û