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32.0,34.3,35.2,42.9,49.1,53.7,55.8,56.0,56.1,60.6,63.4,87.3,110.7,112.8,113.3,115.5,115.7,116.8,118.9,121.6,129.5,132.6,133.0,135.5,143.8,144.7,145.9,147.7,147.9
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1 .     Spathulatol
    ÏàËÆ¶È:76.6%
Acta Botanica Yunnanica          2010          32          281-284
One New Sesqui-lignan from Illicium spathulatum (Ill iciaceae)
LAI Guo-Fang, DONG Xu-Jun, YANG Jian-Kun , LUO Huai-Rong, WANG Yi-Fen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     lappaol A
    ÏàËÆ¶È:76.6%
Chinese Pharmaceutical Journal          2009          44          1287-1290
Studies on Chemical Constituents from Rhaponticum carthamoides (Willd.) Iljin
HUANG Min-fang, LI Ning, NI Hui, JIA Xiao-guang*, LI Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     3-hydroxymethyl-5-(3-hydroxypropyl)-7-methoxy-2-{3-methoxy-4-[1-(3,4-dimethoxybenzyl)-2-hydroxyethyl]phenyl}-2,3-dihydrobenzofuran
C31H38O8     ÏàËÆ¶È:74.1%
Journal of Natural Products          1999          62          1371-1375
New Metabolites from Onopordum illyricum
Alessandra Braca, Nunziatina De Tommasi, Ivano Morelli, and Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     sesquipinsapol B
    ÏàËÆ¶È:72.4%
Chinese Traditional and Herbal Drugs          2010          41          533-536
Â黯¸ùµÄ»¯Ñ§³É·ÖÑо¿
ÌÕ»ªÃ÷;ÍõÁ¥Êé;´ÞÕ¼³¼;ÕÔ´óÇì;ÁõÓÀºê
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     Seslignanoccidentaliol A
C31H38O11     ÏàËÆ¶È:70%
Helvetica Chimica Acta          2010          93          1795-1802
Anthraquinones and Lignans from Cassia occidentalis
Shi-Fei Li, Ying-Tong Di, Yue-Hu Wang, Cheng-Jian Tan, Xin Fang, Yu Zhang, Yong-Tang Zheng, Ling Li, Hong-Ping He, Shun-Lin Li and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     compound 5
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1993          41          1774-1779
Studies on Differentiation-Inducers from Arctium Fructus
Kaoru UMEHARA,Ariko SUGAWA,Masanori KUROYANAGI,Akira UENO and Takao TAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     compound 6
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1993          41          1774-1779
Studies on Differentiation-Inducers from Arctium Fructus
Kaoru UMEHARA,Ariko SUGAWA,Masanori KUROYANAGI,Akira UENO and Takao TAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     (7R, 8R)-7-(4-hydroxy-3-methoxyphenyl)-8-(4-(3-(hydroxymethyl)-5-(3-(E)-hydroxyprop-1-enyl)-7-methoxybenzofuran-2-yl)-2-methoxyphenoxy)propane-7,9-diol
C30H32O10     ÏàËÆ¶È:66.6%
Fitoterapia          2009          80          320-326
Three lignans and one coumarinolignoid with quinone reductase activity from Eurycorymbus cavaleriei
Zhongjun Ma, Xiaoyu Zhang, Lin Cheng, Peng Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     lappaol A
    ÏàËÆ¶È:66.6%
Chinese Journal of Natural Medicines          2006          4          444-447
Chemical Constituents of Antihyperglycemic Active Fraction from Arctium lappa
XU Zhao-Hui; ZHAO Ai-Hua; GAO Xian-Fu; JIA Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     7'-Hydroxyisolappaol A
    ÏàËÆ¶È:66.6%
Pharmazie          2004          59          972-976
Sesquiterpenes, lignans and other constituents from Saussurea macrota
Min Yang, Chun-Ming Wang, Qi Zhang, Yi-Feng Han, and Zhong-Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     trans-5-(3-hydroxypropyl)-7-methoxy-2-[2,3-dihydro-3-hydroxymethyl-7-methoxy-2-(3-methoxy-4-hydroxyphenyl)-benzofuran-5-yl]benzofuran
C29H30O8     ÏàËÆ¶È:65.5%
Planta Medica          2005          71          847-851
Four New Benzofurans from Seeds of Styrax perkinsiae
Qi-Lin Li,Bo-Gang Li,Hua-Yi Qi,Xiao-Ping Gao,Guo-Lin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     erythro¨Cguaiacylglycerol-¦Â-O-4'-(5')-methoxylariciresinol
C31H38O11     ÏàËÆ¶È:65.5%
Natural Product Research          2008          22          990-995
Sesquilignans and dilignans from Campylotropis hirtella (Franch.) Schindl.
Hui-Ying Han; Hong-Wei Liu; Nai-Li Wang; Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     acernikol
    ÏàËÆ¶È:65.5%
Chinese Traditional and Herbal Drugs          2010          41          863-866
Chemical constituents in stems of Schima superba
XU Wen; ZHOU Guang-xiong; DAI Yi; YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     (7R,8S)-dihydrodehydrodiconiferyl alcohol 9'-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:65.5%
Chinese Traditional and Herbal Drugs          2009          40          1039-1042
ɽ·¯µÄ»¯Ñ§³É·ÖÑо¿
»ô³¤ºç;Áººè;ÕÅÇìÓ¢;Íõß“;ÕÔÓñÓ¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     2,3-dihydro-2-(4'-O-¦Â-D-glucopyranosyl-3'-methoxy-phenyl)-3-hydroxymethyl-5-(3-hydroxypropyl)-7-methoxybenzofuran
    ÏàËÆ¶È:65.5%
Chinese Traditional and Herbal Drugs          2003          34          496-498
Studies on water-soluble constituents in rhizome of Polygonum cuspidatum
XIAO Kai; XUAN Li-jiang; XU Ya-ming; BAI Dong-lu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     deltoignan B
C29H30O9     ÏàËÆ¶È:65.5%
Fitoterapia          2012          83          1125-1130
Cytotoxic sesquiterpenes and lignans from Saussurea deltoidea
Jun-Ju Xu, Huo-Qiang Huang, Guang-Zhi Zeng, Ning-Hua Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     (7'R,8'S)-dihydrodehydrodiconiferyl alcohol 4'-O-¦Â-Dglucopyranoside
    ÏàËÆ¶È:65.5%
Chinese Traditional and Herbal Drugs          2011          42          25-30
Lignans and flavonoids from rhizome of Drynaria fortunei
LIANG Yong-hong, YE Min, HAN Jian, WANG Bao-rong, GUO De-an
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     berbikonol
C32H40O11     ÏàËÆ¶È:64.5%
Bioorganic & Medicinal Chemistry Letters          2011          21          2270-2273
Biological evaluation of phenolic constituents from the trunk of Berberis koreana
Ki Hyun Kim,Eunjung Moon,Sang Un Choi , Sun Yeou Kim , Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     compound 4
    ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          1993          41          1774-1779
Studies on Differentiation-Inducers from Arctium Fructus
Kaoru UMEHARA,Ariko SUGAWA,Masanori KUROYANAGI,Akira UENO and Takao TAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     compound 3a
    ÏàËÆ¶È:63.3%
Acta Botanica Sinica          1998          40          466-469
Studies on the Lignans of Polygonum Orientale
ZHENG Shang-Zhen, WANG Ding-Yong, MENG Jun-Cai, SHEN Xu-Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     vitrifol A
C30H34O9     ÏàËÆ¶È:63.3%
Journal of Asian Natural Products Research          2008          10          499-502
One new dihydrobenzofuran lignan from Vitex trifolia
Qiong Gu, Xue-Mei Zhang, Jun Zhou, Sheng-Xiang Qiu and Ji-Jun Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     (7R,8S)-7-(4-hydroxy-3-methoxyphenyl)-8-(4-(3-(hydroxymethyl)-5-(3-(E)-hydroxyprop-1-enyl)-7-methoxybenzofuran-2-yl)-2-methoxyphenoxy)propane-7,9-diol
C30H32O10     ÏàËÆ¶È:63.3%
Fitoterapia          2009          80          320-326
Three lignans and one coumarinolignoid with quinone reductase activity from Eurycorymbus cavaleriei
Zhongjun Ma, Xiaoyu Zhang, Lin Cheng, Peng Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

23 .     picrasmalignan A
C30H30O9     ÏàËÆ¶È:63.3%
Chemistry & Biodiversity          2011          Vol.8          1163-1169
A New Neolignan and a New Sesterterpenoid from the Stems of Picrasma quassioides Bennet
Wei-Hua Jiao, Hao Gao, Feng Zhao, Fei He, Guang-Xiong Zhou, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

24 .     clinopodic acid H
C29H26O12     ÏàËÆ¶È:62.0%
Journal of Natural Products          2009          72          1379-1384
Matrix Metalloproteinase-2 Inhibitors from Clinopodium chinense var. parWiflorum
Toshihiro Murata,Kenroh Sasaki,Kumiko Sato, Fumihiko Yoshizaki, Haruna Yamada, Hiromichi Mutoh, Kaoru Umehara,Toshio Miyase,Tsutomu Warashina,Hiroaki Aoshima, Homare Tabata, and Kouichi Matsubara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

25 .     dihydrodehydrodiconiferyl alcohol 4'-O-¦Â-D-glucoside
C20H24O6     ÏàËÆ¶È:62.0%
Chemical & Pharmaceutical Bulletin          1986          34          4340-4345
Lignans from Trachelospermum asiaticum (Tracheolospermum. II)
FUMIKO ABE and TATSUO YAMAUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

26 .     dihydrodehydrodiconiferyl alcohol 9'-O-glucoside
C26H34O11     ÏàËÆ¶È:62.0%
Chemical & Pharmaceutical Bulletin          1986          34          4340-4345
Lignans from Trachelospermum asiaticum (Tracheolospermum. II)
FUMIKO ABE and TATSUO YAMAUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

27 .     hanultarin
C30H34O9     ÏàËÆ¶È:62.0%
Natural Product Sciences          2009          15          17-21
Lignans from the Roots of Berberis amurensis
Park, Hyun-Bong; Lee, Kyu-Ha; Kim, Ki-Hyun; Lee, Il-Kyun; Noh, Hyung-Jun; Choi, Sang-Un; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

28 .     (7S,8R)-dihydrodehydrodiconiferyl alcohol 4-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:62.0%
Chinese Traditional and Herbal Drugs          2009          40          1039-1042
ɽ·¯µÄ»¯Ñ§³É·ÖÑо¿
»ô³¤ºç;Áººè;ÕÅÇìÓ¢;Íõß“;ÕÔÓñÓ¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

29 .     2,3-¶þÇâ-2-(4-O-¦Â-D ßÁà«ÆÏÌÑÌÇ»ù-3'-¼×Ñõ»ù-±½»ù)-3-ôǼ׻ù-5-(3'-ôÇ»ù±û»ù)-7-¼×Ñõ»ù±½ßòß»à«
    ÏàËÆ¶È:62.0%
Journal of Shenyang Pharmaceutical University          2009          26          279-281
Chemical constituents of the leaves of Crataegus pinnatifida Bge.
HAO Dong-fang, YANG Rui-ping, ZHOU Yu-zhi, CHEN Huan, LI Zhi-feng, PEI Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

30 .     compound 13
    ÏàËÆ¶È:62.0%
Journal of Agricultural and Food Chemistry          2003          51          6165-6172
Lignans and Neolignans from Brassica fruticulosa:  Effects on Seed Germination and Plant Growth
Francesca Cutillo, Brigida D'Abrosca, Marina DellaGreca, Antonio Fiorentino, and Armando Zarrelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

31 .     dihydrodehydrodiconiferylalcohol-¦Â-D-(2'-O-p-hydroxybenzoyl)glucoside
C33H38O13     ÏàËÆ¶È:60.6%
Chemical & Pharmaceutical Bulletin          1998          46          655-662
Pharmacologically Active Components of Viticis Fructus (Vitex rotundifolia). II. The Component Having Analgesic Effects
Emi OKUYAMA,Shigeru FUJIMORI,Mikio YAMAZAKI and Takeshi DEYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

32 .     dumosaol
C30H32O10     ÏàËÆ¶È:60%
Acta Botanica Yunnanica          2005          27(2)          217-222
A New Sesquilignan from Tsuga dumosa
ZHAO You-Xing, LI Cheng-Sen, LUO Xiao-Dong,LIU Yu-Qing,ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

33 .     7',8'-didehydroherpetotriol
C30H30O9     ÏàËÆ¶È:60%
Chinese Chemical Letters          2008          19          1215-1217
Two new lignans from Dipteronia dyeriana
Rong Guo, Min Luo, Chun Lin Long, Ma Lin Li, Zhi Qin Ouyang, Yi Ping Zhou, Yue Hu Wang , Xing Yu Li , Ya Na Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

34 .     L'herpetotriol
C27H19O2(OCH3)3(OH)4     ÏàËÆ¶È:60%
Tetrahedron letters          1978          19          4111-4112
Structure de l'herpetotriol, sesquilignane trimere de l'alcool coniferylique, isole d'herpetospermum caudigerum wall.
Jean Favre-Bonvin, Mourad Kaouadji, Anne-Marie Mariotte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

35 .     (+)lariciresinol-9¡¯-ferulate
C30H32O9     ÏàËÆ¶È:60%
Chemistry & Biodiversity          2011          8          2299-2309
Phenolic Compounds of Abies nephrolepis and Their NO Production Inhibitory Activities (pages 2299¨C2309)
Yong-Li Li, Liang Wu, Dan-Wei Ouyang, Ping Yu, Jia-Han Xia, Yue-Xing Pan, Xian-Wen Yang, Hua-Wu Zeng, Xiang-Rong Cheng, Hui-Zi Jin and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

36 .     saccharumoside A
C34H40O14     ÏàËÆ¶È:58.8%
Journal of Natural Products          2011          74          2472-2476
Phenolic Glycosides from Sugar Maple (Acer saccharum) Bark
Tao Yuan, Chunpeng Wan, Antonio Gonz¨¢lez-Sarr¨ªas, Vamsikrishna Kandhi, Nadja B. Cech, and Navindra P. Seeram
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

37 .     3-benzofuranmethanol-2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-4-methoxy-6-[tetrahydro-2-(3-hydroxy-4-methoxyphenyl)-3-methanol]-2-furanmethyl
C30H35O9     ÏàËÆ¶È:58.6%
Chemical & Pharmaceutical Bulletin          2006          54(11)          1592-1594
Hepatitis B Virus Inhibiting Constituents from Herpetospermum caudigerum
Hai-Long YUAN,Ming YANG,Xian-Yi LI,Rong-Hui YOU,Yi LIU,Jun ZHU,Huan XIE,and Xiao-He XIAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

38 .     grossamide K
C28H29NO7     ÏàËÆ¶È:58.6%
Phytochemistry          2001          58          1219-1223
Lignanamides and other phenolic constituents from the bark of kenaf (Hibiscus cannabinus)
Ana M. L. Seca, Artur M. S. Silva, Armando J. D. Silvestre, Jos¨¦. A. S. Cavaleiro,Fernando M. J. Domingues, Carlos Pascoal-Neto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

39 .     agastinol
C27H28O8     ÏàËÆ¶È:58.6%
Journal of Natural Products          2002          65          414-416
Agastinol and Agastenol, Novel Lignans from Agastache rugosa and Their Evaluation in an Apoptosis Inhibition Assay
Choonghwan Lee, Hyuna Kim, and Yunghee Kho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

40 .     compound 4
    ÏàËÆ¶È:58.6%
Chemical & Pharmaceutical Bulletin          1984          32          4653-4657
Effects of O-Methylation and O-Glucosylation on Carbon-13 Nuclear Magnetic Resonance Chemical Shifts of Matairesinol, (+)-Pinoresinol and (+)-Epipinoresinol
SANSEI NISHIBE,HIROKI TSUKAMOTO and SUEO HISADA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

41 .     herpetin
    ÏàËÆ¶È:58.6%
Journal of Chinese Pharmaceutical Sciences          2005          14          140-143
Herpetin, a New Bioactive Lignan Isolated from Herpetospermum caudigerum
YUAN Hai-long; LIU Yi; ZHAO Yan-ling; and XIAO Xiao-he
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

42 .     isoriccardinquinone B
C29H24O5     ÏàËÆ¶È:58.6%
Natural Product Research          2002          16          167-171
Two New Cyclic Bis(Bibenzyl)s, Isoriccardinquinone A and B from the Liverwort Marchantia Paleacea
May-Ling So; Wing-Hong Chan; Ping-Fang Xia; Yuxin Cui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

43 .     umbroside
C25H32O11     ÏàËÆ¶È:58.6%
Acta Pharmaceutica Sinica          1999          Vol 34          297-300
CHEMICAL CONSTITUENTS FROM THE RHIZOMES OF PHLOMIS UMBROSA TURCZ
Fu Hongzheng (Fu HZ); Liu Shiwang (Liu SW) and Lin Wenhan (Lin WH)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

44 .     cerberalignan E
C30H34O10     ÏàËÆ¶È:58.6%
Phytochemistry          1988          27          3627-3631
Sesqui-,sester-and trilignans from stems of Cerbera manghas and C. odollam
Fumiko Abe,Tatsuo Yamauchi,Alfred S.C. Wan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

45 .     epipinoresinol 4'-O-glucoside
    ÏàËÆ¶È:58.6%
Phytochemistry          1990          29          1971-1980
Lignans of Forsythia intermedia
Maiada M.A. Rahman,Paul M. Dewick,David E. Jackson,John A. Lucas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

46 .     quinquenin L1
    ÏàËÆ¶È:58.6%
Chinese Traditional and Herbal Drugs          2001          32          15-17
Î÷Ñó²Î¾¥Ò¶ÖеÄÒ»ÖÖÄ¾Ö¬ËØ
Íõ½ð»Ô,ºî°ØÁá,Àîϳ,ɳÒÊ!±¾Ð£·ÖÎö²âÊÔÖÐÐÄ,ÀîÎÄ!±¾Ð£·ÖÎö²âÊÔÖÐÐÄ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

47 .     (+)lariciresinol 4-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:58.6%
Chinese Journal of Natural Medicines          2003          1          199-203
Studies on Lignan Constituents of Clematis armandii Franch
HUANG Wen-Wu; KONG De-Yun; YANG Pei-Ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

48 .     woonenoside XI
    ÏàËÆ¶È:58.6%
Chinese Journal of Medicinal Chemistry          2010          20          304-309
The lignans from Daphne giraldii Nitsche
LIU Wen-juan, WANG Li-bo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

49 .     N-(2,5-dimethoxyphenyl)methyl-N-methyl-trans-3-phenylsulfanylacrylamide
C19H21NO3S     ÏàËÆ¶È:58.6%
Heterocycles          2002          57          1063-1077
Synthesis of 1,2-Dihydrobenz[c]azepin-3-one via Acid-catalyzed Cyclization of N-Arylmethyl-N-methyl-3-phenylsulfanylacrylamide
Yoshie Horiguchi,* Toshiaki Saitoh, Tomoko Kashiwagi, Lisa Katura, Mayumi Itagaki, Jun oda, and Takehiro Sano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

50 .     compound 7
C33H34O6Br2     ÏàËÆ¶È:58.6%
Heterocycles          2001          54          259-274
Total Syntheses of Plagiochins A and D, Macrocyclic Bis(bibenzyls), by Pd(0) Catalyzed Intramolecular Stille-Kelly Reaction1
Yoshiyasu Fukuyama,* Hideyuki Yaso, Takashi Mori, Hironobu Takahashi, Hiroyuki Minami, and Mitsuaki Kodama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

51 .     acernikol
C31H38O11     ÏàËÆ¶È:58.0%
Chemical & Pharmaceutical Bulletin          2003          51(1)          62-67
Medicinal Foodstuffs. XXXI. Structures of New Aromatic Constituents and Inhibitors of Degranulation in RBL-2H3 Cells from a Japanese Folk Medicine, the Stem Bark of Acer nikoense
Toshio MORIKAWA, Jing TAO, Kazuho UEDA, Hisashi MATSUDA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

52 .     3-[2-(3,4-dimethoxyphenyl)ethyl]-3,4-dihydro-1-(3-hydroxy-4-methoxyphenyl)-8-methoxy-4-oxo-[1]benzopyrano[3,4-b]pyrrol-7-yl 2,2,2-trichloroethyl sulfate
C31H28Cl3NO11S     ÏàËÆ¶È:58.0%
Bioorganic & Medicinal Chemistry          2011          19          7541-7550
Synthesis, structure¨Cactivity relationships, and mechanism of action of anti-HIV-1 lamellarin ¦Á 20-sulfate analogues
Haruka Kamiyama, Yoshinao Kubo, Hironori Sato, Naoki Yamamoto, Tsutomu Fukuda, Fumito Ishibashi, Masatomo Iwao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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