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²éѯ½á¹û£º¹²²éµ½35¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ 11 . Maculalactone A |
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