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1 .     glucose
C6H12O6     ÏàËÆ¶È:100%
Chinese Journal of Medicinal Chemistry          2011          21          220-225
Chemical constituents from dried fruits of Rubus chingii
XIAO Hong-ming, ZU Ling-bo, LI Shi-ping, WANG Kai-jin, LI Ning*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     3-azido-3-deoxy-¦Á-D-glucopyranosyl-(1¡ú1')-¦Â-D-glucopyranoside
C12H21N3O10     ÏàËÆ¶È:100%
Tetrahedron          2013          69          816-825
Synthesis of 3,3¡ä-neotrehalosadiamine and related 1,1¡ä-aminodisaccharides using disarmed, armed, and superarmed building blocks
Shazia Anjum, Natasha D. Vetter, Joseph E. Rubin, David R.J. Palmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     inotodisaccharide
    ÏàËÆ¶È:100%
Mycosystema          2010          29          897-910
Metabonomic analysis on production of antioxidant secondary metabolites by two geographically isolated strains of Inonotus obliquus in submerged cultures
ZHENG Wei-Fa DAI Yu-Cheng SUN Jing ZHAO Yan-Xia MIAO Kang-Jie PAN Shen-Yuan ZHANG Mei-Mei WEI Jiang-Chun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     compound 11
    ÏàËÆ¶È:83.3%
Chinese Traditional and Herbal Drugs          2010          41          689-692
Chemical constituents from roots of Tinospora sagittata var. yunnanensis
CHENG Chun-mei; DAI Yun; HUANG Xiang-zhong; ZHU Yun; DAI Jian-hui; LIU Xiao-fang; WANG Jiong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     BMY-28251
C12H24N2O10     ÏàËÆ¶È:83.3%
The Journal of Antibiotics          1986          39          1001-1003
3, 3'-NEOTREHALOSADIAMINE (BMY-28251), A NEW AMINOSUGAR ANTIBIOTIC
TAKASHI TSUNO, CHIHARU IKEDA, KEI-ICHI NUMATA, KOJI TOMITA, MASATAKA KONISHI, HIROSHI KAWAGUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     methyl D-glucoside
    ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin          1983          31          3844-3854
Structural Investigation of the Antibiotic Sporaviridin. VIII. Carbon-13 Nuclear Magnetic Resonance Studies of Viridopentaoses and Related Compounds
KENICHI HARADA,SUSUMU ITO and MAKOTO SUZUKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     6-O-Monoester of Karatavikic acid and Sucrose
    ÏàËÆ¶È:75%
Chemistry of Natural Compounds          1996          32          532-534
MODIFICATIONS BASED ON COUMARINS.I. SYNTHESIS OF MONOESTERS OF KARATAVIKIC AND GALBANIC ACIDS WITH SUCROSE
A. F. Artamonova, K. A. Nusipbekova, F. S. Nigmat-llina,G. K. Nikonov, and B. Zh. Dzhienbaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     6-O-Mouomethyl Ester of Galvanic acid and Sucrose
    ÏàËÆ¶È:75%
Chemistry of Natural Compounds          1996          32          532-534
MODIFICATIONS BASED ON COUMARINS.I. SYNTHESIS OF MONOESTERS OF KARATAVIKIC AND GALBANIC ACIDS WITH SUCROSE
A. F. Artamonova, K. A. Nusipbekova, F. S. Nigmat-llina,G. K. Nikonov, and B. Zh. Dzhienbaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     trans-O-Methylmarmesinic acid
C27H38O15     ÏàËÆ¶È:75%
Chemistry of Natural Compounds          1993          29          84-86
SYNTHESIS OF A MONOESTER OF SUCROSE WITH trans-O-METHYLMARMESINIC ACID
A. F. Artamonov, F. S. Nigmatullina,and G. K. Nikonov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     Sucrose
    ÏàËÆ¶È:75%
Chemistry of Natural Compounds          1993          29          84-86
SYNTHESIS OF A MONOESTER OF SUCROSE WITH trans-O-METHYLMARMESINIC ACID
A. F. Artamonov, F. S. Nigmatullina,and G. K. Nikonov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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