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C: 20.4,30.3,49.9,62.8,68.3,74.2,126.7,127.2,127.9,128.0,128.1,128.6,135.9,136.6,168.7,174.1    DMSO
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ÒÀÒÀdyq: ½ð±Ò+10 2015-06-17 09:42:41
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1 .     (1R,5R,6S,8R)-3-benzyloxycarbonyl-8-phenyl-3-aza-2,7,9-trioxabicyclo[4.4.0]decan-5-ol
C20H21NO6     ÏàËÆ¶È:68.7%
Australian Journal of Chemistry          2004          57          187-191
The Synthesis of 3-O-(¦Â-D-Glucopyranosyl)- and 3-O-(¦Â-Laminaribiosyl)-isofagomines, Potent Inhibitors of a 1,3-¦Â-D-Glucan endo-Hydrolase
James M. Macdonald, Maria Hrmova, Geoffrey B. Fincher and Robert V. Stick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (2R,3S)-N-Boc-2-acetyl-3-phenylisoserine benzyl ester
C23H27NO6     ÏàËÆ¶È:68.7%
Chinese Journal of Chemistry          2013          31          31-36
An Efficient Semi-Synthetic Method to Construct Docetaxel via Sterically Crowded Linear Side Chain Esterification
Xin Shen, Jidong Yang, Huaxing Zhan, Hu Wang, Shaohong Wu and Zili Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     1-hydroxy-3-[(1R)-2-hydroxy-1-phenylethyl]-4-methylene-1,3,4,5-tetrahydro-3-benzazepin-2-one
C19H19NO3     ÏàËÆ¶È:64.7%
Zeitschrift f¨¹r Naturforschung B          2010          65          191-196
Enantioselective Synthesis of a 2,2-Disubstituted Tetrahydro-3-benzazepine as Novel NMDA Receptor Antagonist
S. M. Husain, R. Fröhlich, D. Schepmann, and B. W¨¹nsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     benzyl [(4RS,5RS)-1-benzyl-3-oxo-5-(propan-2-yl)pyrazolidin-4-yl]carbamate
C21H25N3O3     ÏàËÆ¶È:64.7%
Helvetica Chimica Acta          2014          97          245-267
A Simple Synthesis of Polyfunctionalized 4-Aminopyrazolidin-3-ones as ¡®Aza-deoxa¡¯ Analogs of D-Cycloserine
Ana Novak, Matej Štefanič, Uroš Grošelj, Martina Hrast, Marta Kasunič, Stanislav Gobec, Branko Stanovnik and Jurij Svete
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     cis-Methyl 1-benzamido-2-phenylcyclohexanecarboxylate
C21H23NO3     ÏàËÆ¶È:64.7%
Chirality          2001          13          48-55
Preparative HPLC resolution of the CIS cyclohexane analogs of phenylalanine
Myriam Al¨ªas, Carlos Cativiela, Ana I. Jim¨¦nez, Pilar L¨®pez, Laureano Oliveros and Michel Marraud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 11c
C23H24N2O4     ÏàËÆ¶È:64.7%
Chinese Journal of Organic Chemistry          2013          33          848-853
Synthesis of Chirl N,P-ligands Derived from L-Proline and Its Application to 1,3-Dipolar Cycloaddition
Chen, Hong Chen, Qian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     N,N,N',N'-Tetrabenzyl-3-oxapentandiamid
C32H32N2O3     ÏàËÆ¶È:62.5%
Helvetica Chimica Acta          1980          63          191-196
Ionophore vom Typ der 3-Oxapentandiamide
Ernö Pretsch, Daniel Ammann, Hans F. Osswald, Mare G¨¹ggi, Wilhelm Simon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     4-acetoxystilbene
C16H14O2     ÏàËÆ¶È:62.5%
Natural Product Research          2007          21          564-573
Synthesis of hydroxystilbenes and their derivatives via Heck reaction
Angela Farina; Carolina Ferranti; Carolina Marra; Marcella Guiso; Giulia Norcia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 11
    ÏàËÆ¶È:62.5%
Phytochemistry          1998          47          1117-1123
Stilbenes, monoterpenes, diarylheptanoids, labdanes and chalcones from Alpinia katsumadai
Koon-Sin Ngo, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     1,7-diphenyl-6(E)-hepten-3-one-5-ol
C19H20O2     ÏàËÆ¶È:62.5%
Journal of Natural Products          1994          Vol 57          230
Novel Nematocidal Agents from Curcuma comosa
Tannis M. Jurgens, Easter G. Frazier, James M. Schaeffer, Tracey E. Jones, Deborah L. Zink, Robert P. Borris, Weerachai Nanakorn, Hans T. Beck, Michael J. Balick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Maculalactone A
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