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1 .     compound 5a
    ÏàËÆ¶È:58.3%
Tetrahedron Letters          2000          41          8293-8296
Asymmetric synthesis of C-6 substituted pipecolic acid derivatives
Sylvie Carbonnel, Catherine Fayet, Jacques Gelas, Yves Troin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Ethyl 2-piperidinobutanoate
C11H21NO2     ÏàËÆ¶È:54.5%
Molecules          2001          6          892-899
Captodative Formyl Enamines in a New Synthesis of Tertiary ¦Á-Amino Esters
Alexandre Y. Rulev, Lyudmila I. Larina and Mikhail G. Voronkov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (3R,5R)-Methyl 3,5-dihydroxydecanoate
C11H22O4     ÏàËÆ¶È:54.5%
Canadian Journal of Chemistry          2009          87          650-661
Chiral ¦Á-substituted allylboronates in a one-potthree-component asymmetric allylic alkylation/carbonyl allylation reaction sequence -Applications to the syntheses of (+)-(3R,5R)-3-hydroxy-5-decanolide and (-)-massoialactone
Lisa Carosi and Dennis G. Hall
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     methyl (¡À)-2-oxo-1-(3-oxopropyl)cyclohexanecarboxylate
C11H16O4     ÏàËÆ¶È:54.5%
Journal of Heterocyclic Chemistry          2003          40          113-120
N-phenyl-substituted pyrrolidines,piperidines and azabicyclics by a tandem reduction-double reductive amination reaction
Richard A. Bunce,Derrick M. Herron,Jason R. Lewis and Sharadsrikar V. Kotturi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     ethyl 4,6-dimethyl-5,7-diphenyl-6-aza-spiro[2.5]octane-1-carboxylate
C24H29NO2     ÏàËÆ¶È:54.5%
Indian Journal of Chemistry Section B          2007          46B          818-822
4-Piperidone ¨C A synthon for spiro-heterocycles
Padmavathi,V; Reddy,T V Ramana; Reddy,K Audisesha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Compound 1
    ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry Letters          1998          8          2375-2380
Combinatorial chemistry of hydantoins
Astrid Boeijen, John A. W. Kruijtzer, Rob M. J. Liskamp
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (R)-3-Methoxymethyl-2-methyleneoctamide
C11H21NO2     ÏàËÆ¶È:54.5%
Chinese Journal of Chemistry          2002          20          1291-1299
Synthesis of Optically Active ¦Â - Alkyl -¦Á- methylene - ¦Ä - butyro -lactones from Enantioselective Biotransformation of Nitriles, an Unusual Inversion of Enantioselectivity†
Sheng-Min Zhao and Mei-Xiang Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (S)-3-Methoxymethyl-2-methylenecxtanoic acid
C11H18O3     ÏàËÆ¶È:54.5%
Chinese Journal of Chemistry          2002          20          1291-1299
Synthesis of Optically Active ¦Â - Alkyl -¦Á- methylene - ¦Ä - butyro -lactones from Enantioselective Biotransformation of Nitriles, an Unusual Inversion of Enantioselectivity†
Sheng-Min Zhao and Mei-Xiang Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3-[(1R,2S)-1-hydroxy-2-methylbutyl]-4-methylfuran-2(5H)-one
C10H16O3     ÏàËÆ¶È:54.5%
Tetrahedron          2003          59          3237-3251
Bioactive butenolides from Streptomyces antibioticus T¨¹ 99: absolute configurations and synthesis of analogs
Gilles Grossmann, Marc Poncioni, Marc Bornand, Benoı̂t Jolivet, Markus Neuburger, Urs S¨¦quin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3-[(1R,2S)-1-hydroxy-2-methylbutyl]-4-methylfuran-2(5H)-one
C10H16O3     ÏàËÆ¶È:54.5%
Tetrahedron          2003          59          3237-3251
Bioactive butenolides from Streptomyces antibioticus T¨¹ 99: absolute configurations and synthesis of analogs
Gilles Grossmann, Marc Poncioni, Marc Bornand, Benoı̂t Jolivet, Markus Neuburger, Urs S¨¦quin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 60
    ÏàËÆ¶È:54.5%
Tetrahedron          1995          51          8835-8852
Synthesis of tricyclopentanoid sesquiterpenes via rearrangement routes: (¡À)-modhephene, (¡À)-epimodhephene and (¡À)-isocomene
Lutz Fitjer, Marita Majewski, Honorato Monz¨®-Oltra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     permetin A
    ÏàËÆ¶È:54.5%
The Journal of Antibiotics          1985          38          1610-1613
ABSOLUTE CONFIGURATION OF THE ¦Â-HYDROXYL FATTY ACID CONSTITUENT OF PERMETIN A
ASAO MURAI, YUSUKE AMINO, TOSHIHIKO ANDO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ethyl 3-hydroxy-3-methylheptanoate
    ÏàËÆ¶È:54.5%
Journal of Chemical Ecology          1996          22          2233-2249
Identification of sex pheromones from cowpea weevil,Callosobruchus maculatus, and related studies withC. analis (coleoptera: Bruchidae)
Thomas W. Phillips, Joel K. Phillips, Francis X. Webster, Rong Tang and Wendell E. Burkholder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     2-methyl-2,5-bornandiol
    ÏàËÆ¶È:54.5%
Annals of Microbiology          2010          60          249-253
Chemical constitutes from endophytic Streptomyces sp. W5 isolated from Trewia nudiflora L.
Guozhu Wei, Na Zhu, Ying Zeng, Yuemao Shen, Peiji Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     1-(tert-butyldimethylsilyloxy)-3,3-bis(methoxymethyl)hex-5-yne
C16H32O3Si     ÏàËÆ¶È:54.5%
Tetrahedron          2013          69          7659-7669
Cyclopropanes in Nicholas reaction: formation of spiroketals with a five-membered and a seven- or an eight-membered ring
Chisato Mukai, Takahiro Kojima, Takamasa Kawamura, Fuyuhiko Inagaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     tetrabutylammonium bis(sec-heptyl)phosphate
    ÏàËÆ¶È:54.5%
Tetrahedron          2013          69          9947-9950
A convenient two-step synthesis of dialkylphosphate ionic liquids
Justyna Kotlarska, Koen Binnemans, Wim Dehaen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (R)-3-(((tert-butyldimethylsilyl)oxy)methyl)-3-methylpentan-1-ol
C13H30O2Si     ÏàËÆ¶È:54.5%
Molecules          2014          19          2213-2225
Synthesis of ∆3-2-Hydroxybakuchiol Analogues and Their Growth Inhibitory Activity against Rat UMR106 Cells
Qun Zhao, Qianqian Xu, Guangsheng Shan, Chao Dong, Hong Zhang and Xinsheng Lei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     n-propyl-3-hydroxyoctanoate
    ÏàËÆ¶È:54.5%
Applied Microbiology and Biotechnology          2013          97          211-222
Polyester hydrolytic and synthetic activity catalyzed by the medium-chain-length poly(3-hydroxyalkanoate)depolymerase from Streptomyces venezuelae SO1
Marta Santos, Joana Gangoiti, Helmut Keul, Martin Möller, Juan L. Serra, Mar¨ªa J. Llama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     3-(1-Hydroxy-2-methylbutyl)-4-methyl-2(5H)-franone
    ÏàËÆ¶È:54.5%
FEMS Microbiology Letters          1995          126          37-42
New butenolides from the photoconductivity screening of Streptomyces antibioticus (Waksman and Woodruff) Waksman and Henrici 1948
Dieter Braun, Niklaus Pauli, Urs Sequin and Hans Zähner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     rac-N-methyl-5-hydroxydecanamide
    ÏàËÆ¶È:54.5%
Flavour and Fragrance Journal          2007          22          531-539
Asymmetric synthesis of ¦Ä-lactones with lipase catalyst
Yasutaka Shimotori, Kazuki Sekine and Tetsuo Miyakoshi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     Ethyl 3-Hydroxy-3-methylheptanoate
    ÏàËÆ¶È:54.5%
Journal of Chemical Ecology          1996          22          2233-2249
Identification of sex pheromones from cowpea weevil,Callosobruchus maculatus, and related studies withC. analis (coleoptera: Bruchidae)
Thomas W. Phillips, Joel K. Phillips, Francis X. Webster, Rong Tang, Wendell E. Burkholder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     ¦Á-{3-[2-hydroxy-3-(N-methyl-N-hydroxyethylcmino)propoxy]propyl}-w-butylpolydimethylsiloxane
    ÏàËÆ¶È:53.8%
Chinese Chemical Letters          2008          19          1196-1198
Synthesis and characterization of ¦Á-{3-[2-hydroxy-3-(N-methyl-N-hydroxy-ethylamino)propoxy]propyl} -w-butylpolydimethylsiloxanes
Hai Feng Sun, Qing Si Zhang , Meng Zhang , Yi Tao Yu, Jian Ping Zong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     compound 1b
    ÏàËÆ¶È:53.8%
Magnetic Resonance in Chemistry          1985          23          137-138
Carbon-13 NMR study of some new macrocycles. 13C chemical shifts of nactin antibiotic models
M. El Malouli Bibout, A. Samat, R. Faure and J. Elguero
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     compound 4
C12H24N4O2     ÏàËÆ¶È:50%
Tetrahedron Letters          2002          43          3935-3937
A convenient synthesis of chiral dioxocyclens and application as chiral solvating agents
Quan Yuan, Enqin Fu, Xiaojun Wu, Maohai Fang, Peng Xue, Chengtai Wu, Jiahua Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     diethyl 4-methylenespiro[4.5]decane-2,2-dicarboxylate
C17H26O4     ÏàËÆ¶È:50%
Molecules          2012          17          4313-4325
Communication: New Methodology for the Synthesis of Thiobarbiturates Mediated by Manganese(III) Acetate
Ahlem Bouhlel, Christophe Curti and Patrice Vanelle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     2-[2-(octylamino)-2-oxoethoxy]acetic acid
C12H22NO4     ÏàËÆ¶È:50%
European Journal of Organic Chemistry          2011                   3959-3969
Hydrolysis and Radiation Stability of m-Xylylene Bis-diglycolamide: Synthesis and Quantitative Study of Degradation Products by HPLC¨CAPCI+
Hitos Gal¨¢n, Mar¨ªa Teresa Murillo, Rosa Sedano, Ana N¨²ñez, Javier de Mendoza, Amparo Gonz¨¢lez-Espartero and Pilar Prados
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     compound S7
C15H34O3Si     ÏàËÆ¶È:50%
Journal of the American Chemical Society          2006          128          11906-11915
Synthetic Studies of Complex Immunostimulants from Quillaja saponaria:  Synthesis of the Potent Clinical Immunoadjuvant QS-21Aapi
Yong-Jae Kim, Pengfei Wang, Mauricio Navarro-Villalobos, Bridget D. Rohde, JohnMark DerryBerry, and David Y. Gin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     2-O-(1',2'-dipentanoyl-sn-glycero)-2-thioxo-2¦Ë5-[1,3,2]-dithiaphospholane
C15H27O5PS3     ÏàËÆ¶È:50%
The Journal of Organic Chemistry          2003          68          7298-7307
Design, Synthesis, and Evaluation of Water-Soluble Phospholipid Analogues as Inhibitors of Phospholipase C from Bacillus cereus
Christopher L. Franklin, Hui Li, and Stephen F. Martin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     TFA¡¤Me2N-D-Ile-Hic-OH
C14H27NO4     ÏàËÆ¶È:50%
Chemistry-A European Journal          2011          17          13544-13552
Total Synthesis, Stereochemical Assignment, and Antimalarial Activity of Gallinamide A
Trent Conroy, Jin T. Guo, Prof. Roger G. Linington, Prof. Nicholas H. Hunt and Dr. Richard J. Payne
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     (4R,2'S)-4-(2'-Hydroxyheptyl)-N(5)-methyl-1,5-diazocan-2-one
C14H28N2O2     ÏàËÆ¶È:50%
The Journal of Organic Chemistry          2012          77          9724-9737
Absolute Configuration Assignment by Asymmetric Syntheses of the Homalium Alkaloids (−-(R,R,R)-Hoprominol and (−-(4¡äS,4¡åR,2‴R)-Hopromalinol
Stephen G. Davies, James A. Lee, Paul M. Roberts, Jeffrey P. Stonehouse, and James E. Thomson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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