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1 .     methyl 2-ethyl-5-oxopyrrolidine-3-carboxylate
C8H13NO3     ÏàËÆ¶È:62.5%
Journal of Heterocyclic Chemistry          2008          45          1251-1253
Convenient preparations of 2-alkyl-5-oxopyrrolidine-3-carboxylic acids
Anna D. Photiadou,Christos I. Stathakis and John K. Gallos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Compound 6c
C24H37N3SO5     ÏàËÆ¶È:61.5%
Bioorganic & Medicinal Chemistry Letters          2006          16          2067-2070
Fluorescent glycosidase inhibiting 1,5-dideoxy-1,5-iminoalditols
Peter Greimel, Herwig Häusler, Inge Lundt, Karen Rupitz, Arnold E. St¨¹tz, Chris A. Tarling, Stephen G. Withers, Tanja M. Wrodnigg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Ethyl (1S*,5S*,6S*)-6-methoxy-3-azabicyclo[3.3.1]nonane-1-carboxylate
C12H21NO3     ÏàËÆ¶È:61.5%
Tetrahedron          2012          68          5759-5778
A tandem Diels¨CAlder/Mannich approach to the synthesis of AE and ABE ring analogues of Delphinium alkaloids
Kirsten J. Goodall, Margaret A. Brimble, David Barker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (¡À) 2-(2-hydroxy-3-(octylsulfonamido)-cyclopentyl)-acetic acid
C15H29NO5S     ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry          2010          18          6470-6479
Design, synthesis, and biological evaluation of conformationally constrained glycerol 3-phosphate acyltransferase inhibitors
Edward A. Wydysh, Aravinda Vadlamudi, Susan M. Medghalchi, Craig A. Townsend
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     methyl (1R,2R,5R)-1-[(1,3-dioxolan-2-yl)methyl]-2-isopropyl-5-methylcyclopentanecarboxylate
C14H22O4     ÏàËÆ¶È:57.1%
European Journal of Organic Chemistry          2011                   5167-5175
Enantioselective Synthesis of the Unnatural Enantiomers of the Fungal Sesquiterpenoids Acorenone and Trichoacorenol
Nelson L. Brock and Jeroen S. Dickschat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (2R,3S)-1-(tert-butoxycarbonyl)-2-hexylpyrrolidine-3-carboxylic a cid
C16H29NO4     ÏàËÆ¶È:57.1%
European Journal of Organic Chemistry          2010                   3395-3406
Diastereoselective Access to Enantiomerically Pure cis-2,3-Disubstituted Pyrrolidines
Pierre-Olivier Delaye, Tarun K. Pradhan, ¨¦milie Lambert, Jean-Luc Vasse and Jan Szymoniak
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (2R,3S,5S,6R)-cis-2,3-cis-5,6-diepoxyheptadecanol
C17H32O3     ÏàËÆ¶È:57.1%
Journal of Chemical Ecology          2004          30          1225-1244
Chiral Synthesis of (Z)-3-cis-6,7-cis-9, 10-Diepoxyhenicosenes, Sex Pheromone Components of the Satin Moth, Leucoma salicis
Priyantha D. C. Wimalaratne, Keith N. Slessor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     1-n-Butyl-4-(5'-formyl-2'-furyl)methyl succinate
C14H18O6     ÏàËÆ¶È:57.1%
Journal of Agricultural and Food Chemistry          2006          54          6398-6402
New Constituents from Noni (Morinda citrifolia) Fruit Juice
Volodymyr Samoylenko, Jianping Zhao, D. Chuck Dunbar, Ikhlas A. Khan, James W. Rushing, and Ilias Muhammad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     hexyl-6-(2,5-dioxopyrrolidin-1-yl)-2-(2-oxopyrrolidin-1-yl)hexanoate
C20H32O5N2     ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2010          18          73-79
Synthesis, physico-chemical properties and penetration activity of alkyl-6-(2, 5-dioxopyrrolidin-1-yl)-2-(2-oxopyrrolidin-1-yl)hexanoates as potential transdermal penetration enhancers
Katerina Brychtova, Josef Jampilek, Radka Opatrilova, Ivan Raich, Oldrich Farsa, Jozef Csollei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     andrachcinidine
C13H25NO2     ÏàËÆ¶È:53.8%
Journal of Natural Products          2000          63          762-764
Alkaloids of Andrachne aspera
Sibel Mill and Claude Hootele
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     cyclopropanes IIIa
    ÏàËÆ¶È:53.8%
Chemistry of Natural Compounds          1989          25          231-236
13C NMR SPECTRA OF BIOLOGICALLY ACTIVE COMPOUNDS. Vll. STEREOISOMERS OF CYCLOPROPANECARBOXYLIC ESTERS OF THE PYRETHROID SERIES
L. M. Khalilov, A. A. Fatykhov,V. S. Sultanova, F. Z. Makaev,F. Z. Galin, G. A. Tolstikov, and A. A. Panasenko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     1,5,5,9-Tetramethylspiro[3.5]nonan-l-ol
C13H24O     ÏàËÆ¶È:53.8%
Helvetica Chimica Acta          1980          63          154-190
Photochemische Reaktionen. 106. Mitteilung. Zur Photochemie tetraalkylsubstituierter ¦Ã-Keto-olefine
Jacob Berger, Michikazu Yoshioka, Markus P. Zink, Hans R. Wolf, Oskar Jeger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (N2-(2'S)-Bis(1',3'-methoxycarbonyl)ethyl),N5-tert-butyloxycarbonyl)-1,2,5-thiadiazolidine-1,1-dioxide
C13H22 N2O8S     ÏàËÆ¶È:53.8%
Molecules          2005          10          1387-1398
N, N¡¯-Substituted 1, 2, 5 Thiadiazolidine 1, 1-Dioxides: Synthesis, Selected Chemical and Spectral Proprieties and Antimicrobial Evaluation
A. Bendjeddou, R. Djeribi, Z. Regainia and N. Aouf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Ethyl-6-(2,5-dioxopyrrolidin-1-yl)-2-(2-oxopyrrolidin-1-yl)hexanoate
C16H24O5N2     ÏàËÆ¶È:53.8%
Molecules          2009          14          3019-3029
Coupling Reactions of ¦Á-Bromocarboxylate with Non-Aromatic N-Heterocycles
Katerina Brychtova, Barbora Slaba, Lukas Placek, Josef Jampilek, Ivan Raich and Jozef Csollei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3-cyclohexyl-1-methyl-2-(2-propyl)imidazolidin-4-one
C10H20N2O     ÏàËÆ¶È:53.8%
Heterocycles          2004          63          1165-1173
A Solvent-free Method for Substituted Imidazolidin-4-ones Synthesis
Jir¨ª Posp¨ªsil and Milan Pot¨¢cek*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Compound 12
    ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry Letters          2000          10          1585-1588
4-Amino-1,2-dithiolane-4-carboxylic acid (Adt) as cysteine conformationally restricted analogue. synthetic protocol for Adt containing peptides
Enrico Morera, Marianna Nalli, Francesco Pinnen, Domenico Rossi, Gino Lucente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Compound 1d
C29H40N4O7S     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry Letters          2006          16          2067-2070
Fluorescent glycosidase inhibiting 1,5-dideoxy-1,5-iminoalditols
Peter Greimel, Herwig Häusler, Inge Lundt, Karen Rupitz, Arnold E. St¨¹tz, Chris A. Tarling, Stephen G. Withers, Tanja M. Wrodnigg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Compound 2d
C29H40N4O7S     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry Letters          2006          16          2067-2070
Fluorescent glycosidase inhibiting 1,5-dideoxy-1,5-iminoalditols
Peter Greimel, Herwig Häusler, Inge Lundt, Karen Rupitz, Arnold E. St¨¹tz, Chris A. Tarling, Stephen G. Withers, Tanja M. Wrodnigg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Compound 9a
    ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry Letters          1998          8          705-710
Syntheses and kinetic evaluation of hydroxamate-based peptide inhibitors of glyoxalase I
Hoa D. Ly, Susan L. Clugston, Peter B. Sampson, John F. Honek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     1,1,1-Tris-(Boc-L-methioninemehyl)-ethane
    ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry Letters          1999          9          781-786
Synthesis and electrochemical study of a new chiral tris-catecholamide analogue of enterobactin
N. Cheraïti, M. E. Brik, A. Gaudemer, G. Kunesh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-12-10 10:08:39
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