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13C NMR (126 MHz, MeOD) ¦Ä
5.16,9.58,12.58,17.64,21.91,22.20,23.11,26.43,28.29,28.64,28.92,29.78, 31.24,38.32,44.73,46.67,46.84,47.01,47.19, 47.36, 47.53,47.70,67.30,68.71,68.78,93.02,100.80,101.70, 103.34,105.64,114.34,114.49,115.11,128.03, 129.06,130.57,130.77, 131.73,155.71,156.43,160.49,161.01,164.03,167.54,198.47

[ Last edited by ׿Խ_ÏÈ·æ on 2015-6-4 at 13:07 ]
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xieliting: ½ð±Ò+10 2015-06-04 19:23:07
²éѯ½á¹û£º¹²²éµ½3¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     desmodianone E
C26H24O6     ÏàËÆ¶È:60.8%
Phytochemistry          2003          64          599-602
Three isoflavanones with cannabinoid-like moieties from Desmodium canum
B. Botta, E. Gacs-Baitz, V. Vinciguerra, G. Delle Monache
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     Compound 4
C46H62O14     ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry Letters          2007          17          5101-5106
OSW-1 analogues: Modification of the carbohydrate moiety
Theophile Tschamber, Solange Adam, Yuji Matsuya, Seiji Masuda, Noriko Ohsawa, Sakiko Maruyama, Keiichi Kamoshita, Hideo Nemoto, Jacques Eustache
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     benzyl 7¦Á-benzoyloxy-3¦Á-[N-Boc-N,O-(4-methoxybenzylidene)-¦Â-phenylisoserinoyl]-12¦Á-trifluoroacetoxy-5¦Â-cholan-24-oate
C62H72F3NO12     ÏàËÆ¶È:60%
European Journal of Organic Chemistry          2005          2005          3952-3961
The Design and Synthesis of New Steroidal Compounds as Potential Mimics of Taxoids
Fanny Roussi, Quoc Anh Ngo, Sylviane Thoret, Françoise Gu¨¦ritte and Daniel Gu¨¦nard
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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