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13C NMR (75 MHz, MeOD) ¦Ä 11.9, 12.1, 15.4, 30.7,  64.2, 65.1, 72.8, 76.3, 84.8, 108.5, 110.4, 131.2, 139.1, 167.5.
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è÷É«ÐÄÇç: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-04-12 19:10:18
1 .     1-(1,3-Anhydro-¦Â-D-psicofuranosyl)thymine
    ÏàËÆ¶È:57.1%
Tetrahedron Letters          2002          43          6553-6555
Synthesis of anhydro psicofuranosyl nucleosides
Jarkko Roivainen, Jouko Vepsäläinen, Alex Azhayev, Igor A. Mikhailopulo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     2,6-dimethyl-2E,6E-octadienoic acid 1,6'-lactone 8-¦Â-D-glucopyranoside
    ÏàËÆ¶È:50%
Chinese Chemical Letters          2000          11          709-710
A New Monoterpene Glycoside from Swertia punicea
Xin MING, Ming Hua QIU, Rui Lin NI',Guo Lin ZHANG
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     3-{[(1Z)-7-hydroxyhexadeca-1-ene-3,5-diynyl]oxy}-1,2-propanediol
C19H30O4     ÏàËÆ¶È:50%
Journal of Natural Products          1990          Vol 53          732
Diyne Enol Ethers of Glycerol from a New Zealand Sponge, Petrosia hebes
Nigd B. Perry, Eleanor G. Becker, John W. Blunt, Robin J. Lake, Murray H. G. Munro
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     2,6-dimethyl-8-hydroxyl-2,6-octadienica cid-8-O-¦Â-D-glucopynanoside
    ÏàËÆ¶È:50%
Chinese Traditional and Herbal Drugs          2004          35          1084-1086
Chemical constituents of Elsholtzia bodinieri
CHEN Ri-lai; ZHOU Chun-xiang; CHEN Hai-yun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     ethyl 1-tert-butyl-1,4-dihydro-4-oxo-3-quinolinecarboxylate
C16H19NO3     ÏàËÆ¶È:50%
Journal of Heterocyclic Chemistry          2011          48          620-625
Ethyl 1,4-dihydro-4-oxo-3-quinolinecarboxylates by a tandem addition-elimination-SNAr reaction
Richard A. Bunce, Eric J. Lee and Matthew T. Grant
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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