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4ºÅ
13C NMR (101 MHz, MeOD) ¦Ä 170.89 (s, 7H), 153.34 (s, 14H), 144.41 (s, 9H), 128.43 (s, 15H), 112.50 (s, 8H), 105.09 (s, 1H), 100.96 (s, 3H), 100.12 (s, 16H), 98.16 (s, 15H), 78.02 (s, 13H), 77.99 ¨C 77.35 (m, 22H), 75.09 ¨C 74.42 (m, 20H), 73.25 (s, 6H), 71.67 ¨C 71.08 (m, 20H), 62.46 (d, J = 8.7 Hz, 21H), 61.27 (s, 16H), 57.33 (s, 1H), 55.49 (s, 3H), 49.87 (s, 1H), 49.74 (d, J = 20.6 Hz, 12H), 49.32 (d, J = 21.5 Hz, 43H), 49.03 (s, 7H), 49.03 (s, 19H), 49.07 ¨C 48.52 (m, 94H), 48.57 (s, 14H), 48.47 (d, J = 21.5 Hz, 23H), 46.78 (s, 16H), 39.52 (s, 15H), 36.37 (s, 15H).

5ºÅ
13C NMR (101 MHz, MeOD) ¦Ä 150.78 (s, 2H), 148.91 (d, J = 26.6 Hz, 3H), 147.32 (t, J = 13.6 Hz, 3H), 137.35 (d, J = 9.5 Hz, 2H), 133.67 (s, 2H), 131.26 (s, 1H), 120.46 ¨C 119.60 (m, 6H), 119.35 (s, 1H), 117.83 (s, 3H), 116.09 (s, 5H), 111.54 (d, J = 5.9 Hz, 3H), 110.97 (s, 3H), 110.53 (s, 1H), 102.68 (s, 3H), 88.92 (s, 1H), 87.36 (s, 3H), 86.98 (s, 2H), 83.43 (s, 1H), 78.04 (s, 4H), 77.69 (s, 5H), 74.80 (s, 5H), 72.60 (d, J = 4.8 Hz, 6H), 71.97 (s, 2H), 71.23 (s, 4H), 70.64 (s, 2H), 62.42 (s, 4H), 56.74 (s, 5H), 56.44 (s, 7H), 55.58 (s, 2H), 55.27 (d, J = 17.6 Hz, 5H), 51.12 (s, 1H), 49.64 (s, 5H), 49.47 (s, 2H), 49.32 (d, J = 21.5 Hz, 41H), 49.00 (s, 32H), 48.83 (s, 4H), 48.68 (d, J = 21.4 Hz, 38H), 48.36 (s, 5H).

6ºÅ
13C NMR (101 MHz, MeOD) ¦Ä 78.04 (s, 2H), 77.72 (s, 2H), 77.39 (s, 2H), 48.59 (s, 1H), 48.37 (s, 3H), 48.16 (s, 5H), 47.95 (s, 6H), 47.74 (s, 5H), 47.52 (s, 3H), 47.31 (s, 1H).

7ºÅ
13C NMR (101 MHz, MeOD) ¦Ä 105.51 (s, 1H), 104.56 (s, 2H), 101.22 (s, 3H), 99.68 (d, J = 5.4 Hz, 3H), 77.86 (s, 8H), 76.10 (s, 2H), 75.00 (s, 10H), 73.39 (d, J = 16.8 Hz, 14H), 71.80 (s, 5H), 71.46 (s, 9H), 69.79 (s, 1H), 67.28 (s, 2H), 62.40 (s, 10H), 57.63 (d, J = 9.2 Hz, 1H), 55.80 (s, 2H), 49.53 (d, J = 21.4 Hz, 15H), 49.42 ¨C 49.40 (m, 4H), 49.12 (d, J = 17.4 Hz, 40H), 49.04 (s, 4H), 48.89 (d, J = 21.5 Hz, 63H), 48.61 (s, 3H), 48.47 (d, J = 21.4 Hz, 18H).

8ºÅ
13C NMR (101 MHz, MeOD) ¦Ä 196.26 (s, 1H), 156.30 (s, 1H), 126.69 (s, 1H), 125.16 (s, 2H), 116.66 (s, 2H), 112.18 (s, 1H), 56.50 (s, 1H), 49.64 (s, 9H), 49.42 (s, 31H), 49.21 (s, 32H), 49.00 (s, 51H), 48.79 (s, 33H), 48.57 (s, 18H), 48.36 (s, 7H).

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À×»À: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл£¡ 2015-03-28 16:41:50
44

1 .     genameside C
C23H34O15     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          2005          53(10)          1342-1344
Iridoid Glucosides from the Fruit of Genipa americana
Masateru ONO,Masami UENO,Chikako MASUOKA,Tsuyoshi IKEDA,and Toshihiro NOHARA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     10,6'-di-O-(1-methoxy-1-methylethyl)-geniposide
C25H40O12     ÏàËÆ¶È:57.1%
Journal of Natural Products          1999          62          1646-1654
Stereoselective Hydrogenation and Ozonolysis of Iridoids. Conversion into Carbocyclic Nucleoside Analogues
Henrik Franzyk, and Frank R. Stermitz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     Genipin 1-O-¦Â-D-isomaltoside
C23H34O15     ÏàËÆ¶È:57.1%
Phytochemistry          2009          70          779-784
Iridoid glycosides from Gardeniae Fructus for treatment of ankle sprain
Quan Cheng Chen, Wei Yun Zhang, UiJoung Youn, HongJin Kim, IkSoo Lee, Hyun-Ju Jung, MinKyun Na, Byung-Sun Min, KiHwan Bae
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     genipin-gentiobioside
    ÏàËÆ¶È:57.1%
Journal of Chinese Medicinal Materials          2012          35          1950-1952
Study on the Chemical Constituents of Fructus Gardeniae
HUANG Tao, MU Shu-zhen, HAO Xiao-jiang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     genipin-gentiobioside
    ÏàËÆ¶È:57.1%
Chinese Traditional and Herbal Drugs          2014          45          16-22
Chemical constituents from root tubers of Rehmannia glutinosa
LIU Yan-fei, LIANG Dong, LUO Huan, HAO Zhi-you, WANG Yan, ZHANG Chun-lei, CHEN Ruo-yun, YU De-quan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     genameside C
    ÏàËÆ¶È:57.1%
Chinese Traditional and Herbal Drugs          2014          45          16-22
Chemical constituents from root tubers of Rehmannia glutinosa
LIU Yan-fei, LIANG Dong, LUO Huan, HAO Zhi-you, WANG Yan, ZHANG Chun-lei, CHEN Ruo-yun, YU De-quan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     6''-O-trans-Sinapoylgenipin gentiobioside
C34H44O19     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          2011          59          803-833
Naturally Occurring Iridoids and Secoiridoids. An Updated Review, Part 4
Biswanath DINDA, Sudhan DEBNATH, and Rajarshi BANIK
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     scyphiphorins B
C26H38O12     ÏàËÆ¶È:53.5%
Helvetica Chimica Acta          2007          Vol. 90          1718
Scyphiphorins A and B, Two New Iridoid Glycosides from the Stem Bark of a Chinese Mangrove Scyphiphora hydrophyllacea
Shu-Hong Tao, Jun Wu, Shu-Hua Qi, Si Zhang, Min-Yi Li, and Qing-Xin Li
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
55

1 .     Mananthoside K
C36H44O15     ÏàËÆ¶È:57.8%
Journal of Asian Natural Products Research          2008          10          228-232
Three new lignan glycosides from Mananthes patentiflora
Jun-Mian Tian, Hong-Ping He, Ying-Tong Di, Xian-Wen Yang, Zhu-Lin Gao and Xiao-Jiang Hao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     zanthpodocarpin E
C41H40O15     ÏàËÆ¶È:56.0%
Bioorganic & Medicinal Chemistry Letters          2014          24          4667-4671
Characterization and biological evaluation of six new dimeric lignans with an unusual ¦Á,¦Â-unsaturated ketone motif from Zanthoxylum simulans
Jun-Feng Wang, Yi-Hui Deng, Sheng-Hui Yang, Yan-Qun Liu, Yue-Hu Wang, Wei-Wei Pan, Xiao-Jiang Zhou
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     pinoresinol O-[6-O-(E)-caffeoyl]-¦Â-D-glucopyranoside
C35H38O14     ÏàËÆ¶È:55.2%
Chemical & Pharmaceutical Bulletin          2002          50(5)          583-589
Studies on the Constituents from the Aerial Part of Baccharis dracunculifolia DC. II
Yoshimi NAGATANI, Tsutomu WARASHINA, and Tadataka NORO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     (+)-pinoresinol 4'-O-¦Â-D-glucopyranosyl(1¡ú2)-O-[¦Â-D-glucopyranosyl(1¡ú6)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:55.2%
Heterocycles          1993          36          933-936
Structure of Novel Antioxidative Lignan Triglucoside Isolated from Sesame Seed
Hirotaka Katsuzaki, Shunro Kawakishi, and Toshihiko Osawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     samsesquinoside
C37H46O16     ÏàËÆ¶È:55.2%
Fitoterapia          2014          94          29-35
New lignans from the bioactive fraction of Sambucus williamsii Hance and proliferation activities on osteoblastic-like UMR106 cells
Hui-hui Xiao, Yi Dai, Man-sau Wong, Xin-sheng Yao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     compound 1
C36H40O14     ÏàËÆ¶È:55.2%
Journal of Agricultural and Food Chemistry          2007          55          6460-6465
Inhibitory Activity against Tobacco Mosaic Virus (TMV) Replication of Pinoresinol and Syringaresinol Lignans and Their Glycosides from the Root of Rhus javanica var. roxburghiana
Ming-An Ouyang, Yung-Shung Wein, Zhen-Kun Zhang, and Yueh-Hsiung Kuo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     dracunculifoside R
C36H44O15     ÏàËÆ¶È:52.6%
Chemical & Pharmaceutical Bulletin          2002          50(5)          583-589
Studies on the Constituents from the Aerial Part of Baccharis dracunculifolia DC. II
Yoshimi NAGATANI, Tsutomu WARASHINA, and Tadataka NORO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     incanoside D
C37H50O20     ÏàËÆ¶È:52.6%
Chemical & Pharmaceutical Bulletin          2000          48(7)          1075-1078
Three New Phenylethanoid Glycosides from Caryopteris incana and Their Antioxidative Activity
JianJun GAO,Kiharu IGARASHI,and Manabu NUKINA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     chionoside B
C36H48O20     ÏàËÆ¶È:52.6%
Chemical & Pharmaceutical Bulletin          2010          58          703-711
Phenylethanoid and Iridoid Glycosides in the New Zealand Snow Hebes (Veronica, Plantaginaceae)
Rilka M. Taskova, Tetsuo Kokubun, Ken G. Ryan, Phil John Garnock-Jones and Soren Rosendal Jensen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

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À×»À: ½ð±Ò+30, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл£¡ 2015-03-28 16:42:08
66

1 .     compound 5
C6H13N2O2PS     ÏàËÆ¶È:50%
Tetrahedron Letters          2000          41          3073-3076
Alkylthiylation of triquinphosphoranes by disulfides: an entry to chiral thiatriquinphosphoranes
Caroline Marchi, G¨¦rard Buono
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     (3R,4S,5R)-5-amino-1-(tert-butoxycarbonyl)-3,4-dihydroxypiperidine
C10H20O4N2     ÏàËÆ¶È:50%
European Journal of Organic Chemistry          2011                   2230-2234
Concise Route to (¨C)- and (+)-Aphanorphine
Mohamed Medjahdi, Jos¨¦ C. Gonz¨¢lez-G¨®mez, Francisco Foubelo and Miguel Yus
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     compound 39
    ÏàËÆ¶È:50%
European Journal of Organic Chemistry          2010                   5263-5273
An Anomeric Effect Drives the Regiospecific Ring-Opening of 1,3-Oxazolidines under Acetylating Conditions
R. Fernando Mart¨ªnez, Mart¨ªn ¨¢valos, Reyes Babiano, Pedro Cintas, Jos¨¦ L. Jim¨¦nez, Mark E. Light, Juan C. Palacios and Esther M. S. P¨¦rez
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

77
1 .     compound 5
    ÏàËÆ¶È:59.0%
Magnetic Resonance in Chemistry          1993          31          599-605
1H and 13C NMR data for 2-O-, 3-O-and 2,3-di-O-glycosylated methyl ¦Á-and ¦Â-D-galactopyranosides
Alexander S. Shashkov, Nikolay E. Nifant'ev, Vera Yu. Amochaeva and Nikolay K. Kochetkov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     2,6-dimethoxy-4[(1E)-prop-1-enyl]phenyl O-¦Á-L-rhamnopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside
C23H34O12     ÏàËÆ¶È:54.5%
Helvetica Chimica Acta          2006          Vol. 89          884
Study on the Chemical Constituents of Daphniphyllum angustifolium
Haiyun Bai and Lihong Hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     rhyncoside D
C21H32O13     ÏàËÆ¶È:54.5%
Chemical & Pharmaceutical Bulletin          2007          55(8)          1175-1180
Rhyncosides A¡ªF, Phenolic Constituents from the Chinese Mangrove Plant Bruguiera sexangula var. rhynchopetala
Shuyun BAO,Yi DING,Zhiwei DENG,Peter PROKSCH,d an Wenhan LIN
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     methyl gentiobioside
    ÏàËÆ¶È:54.5%
Chemical & Pharmaceutical Bulletin          1989          37          2727-2730
Two New Triterpenoid Glycosides from the Leaves of Schefflera octophylla
Junichi KITAJIMA and Yasuko TANAKA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     6'-O-¦Â-D-Glucopyranosyltheviridoside
C23H34O16     ÏàËÆ¶È:54.5%
Phytochemistry          1995          38          793-794
Minor iridoids from Thevetia peruviana
Fumiko Abe, Tatsuo Yamauchi, Shoji Yahara, Toshihiro Nohara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     5-O-Allosylantirrinoside
    ÏàËÆ¶È:54.5%
Phytochemistry          1993          32          1068-1070
5-O-Allosylantirrinoside from Linaria species
Emilia Ilieva, Nedjalka Handjieva, Stefan Spassov, Simeon Popov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     3-O-[¦Â-D-glucopyranosyl (1¡ú3)-¦Á-L-rhamnopyranosyl (1¡ú4)-¦Â-D-xylopyranosyl] hederagenin
    ÏàËÆ¶È:54.5%
Turkish Journal of Chemistry          2002          26          947-954
New Triterpenic Saponins from Cephalaria transsylvanica
S¨¹HEYLA KIRMIZIG¨¹L, H¨¹SEYİN ANIL
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     compound 2
    ÏàËÆ¶È:54.5%
Canadian Journal of Chemistry          1990          68          1238-1250
NMR and conformational study of branched oligosaccharides containing 2,3-disubstituted residues of ¦Á-L-rhamnose
Grigory M. Lipkind, Nikolay E. Nifant'ev, Alexander S. Shashkov, Nikolay K. Kochetkov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     8-methoxycarbonyloctyl O-(2-acetamido-2-deoxy-¦Â-D-glucopyranosyl)-(1¡ú2)-O-(3,4-di-O-benzyl-¦Á-L-rhamnopyranosyl)-(1¡ú2)-3,4-di-O-benzyl-¦Á-L-rhamnopyranoside
C58H77NO16     ÏàËÆ¶È:54.5%
Canadian Journal of Chemistry          1979          57          3073-3079
Artificial carbohydrate antigens: the synthesis of the tetrasaccharide repeating unit of Shigella flexneri O antigen
Staffan Josephson, David R. Bundle
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
88

1 .     ferulaldehyde
C10H10O3     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2009          45          234-236
MONO-AROMATIC CONSTITUENTSOF Dendrobium longicornu
Jiang-Tao Li, Ben-Lin Yin, Ying Liu, Li-Qin Wang, and Ye-Gao Chen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     Coniferaldehyde
    ÏàËÆ¶È:50%
Korean Journal of Pharmacognosy          2009          40(4)          326-333
Phytochemical Studies on Lonicera Caulis (2) - Aliphatic and Phenolic Compounds
Kim, Ju-Sun; Yean, Min-Hye; Seo, Hyun-Kyu; Lee, Je-Hyun; Kang, Sam-Sik
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     acetovanillone
    ÏàËÆ¶È:50%
Chinese Traditional and Herbal Drugs          2005          36          1604-1607
Effect of phenolic acids isolated from Sambucus williamsii on proliferation and differentiation of rat osteoblastic UMR106 cells
YANG Xu-juan; WONG Man-sau; WANG Nai-li; CHAN Sun-chi; YAO Xin-sheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     coniferyl aldehyde
    ÏàËÆ¶È:50%
Chinese Traditional and Herbal Drugs          2011          42          437-439
Chemical constituents of Opuntia milpa (I)
LUO Chuan, ZHANG Wan-nian
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     coniferyl aldehyde
C11H11O3     ÏàËÆ¶È:50%
Natural Product Research and Development          2014          26          1780-1784
Chemical Constituents from the Fruits of Capparis masaikai
LIAO Jin-hua, HU Xu-jia*, YUAN Chun-mao, HE Hong-ping, DI Ying-tong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     4-Phenylphenol
    ÏàËÆ¶È:50%
Molecules          2012          17          12121-12139
Suzuki-Miyaura Reactions Catalyzed by C2-Symmetric Pd-Multi-Dentate N-Heterocyclic Carbene Complexes
Lan Jiang, Fengjun Shan, Zhengning Li and Defeng Zhao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     coniferyl aldehyde
    ÏàËÆ¶È:50%
Chinese Traditional and Herbal Drugs          2012          43          2346-2350
Chemical constituents from fruits of Vitex negundo
ZHAO Xiang-xiang; ZHENG Cheng-jian; QIN Lu-ping
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     2-ôÇ»ù-5-¼×Ñõ»ù-±½±ûϩȩ
    ÏàËÆ¶È:50%
China Journal of Chinese Materia Medica          2012          37          2092-2099
Non-anthraquinones constituents from the roots of Knoxia valerianoides
ZHAO Feng; WANG Sujuan; WU Xiuli; YU Yang; YUE Zhenggang; LIU Bo; LIN Sheng; ZHU Chenggen; YANG Yongchun; SHI Jiangong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     coniferaldehyde
    ÏàËÆ¶È:50%
Journal of the Korean Society for Applied Biological Chemistry          2012          55          433-437
Cytotoxic Compounds from the Fruits of Vitex rotundifolia against Human Cancer Cell Lines
Haejin Kim, Jin-Mu Yi, No Soo Kim, You Jin Lee, Jinhee Kim, Dal-Seok Oh, Se-Mi Oh, Ok-Sun Bang, Jun Lee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     aldehyde
    ÏàËÆ¶È:50%
Chinese Traditional and Herbal Drugs          2014          45          1373-1377
Chemical constituents from Gnaphlium affine
LI Sheng-hua
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
ÄáºÕ
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