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13C NMR:  28.25, 28.47, 29.97, 52.07, 52.93, 56.51, 57.12, 68.46, 70.73, 71.85, 74.13, 96.30, 104.02, 126.18, 126.98, 127.87, 128.37, 128.87, 129.87, 133.96, 141.30, 159.10, 168.48, 196.28
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1 .     Compound 8
C28H32F3N6O7     ÏàËÆ¶È:62.5%
Chemistry ¨C An Asian Journal          2011          6          3260-3269
Thermoresponsive Supramolecular Dendronized Polymers
Jiatao Yan, Wen Li, Kun Liu, Dalin Wu, Feng Chen, Peiyi Wu, and Afang Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     compound 30
C31H33O6N     ÏàËÆ¶È:55.5%
Phytochemistry          2001          58          775-787
Synthesis and antifeedant properties of N-benzoylphenylisoserinates of Lactarius sesquiterpenoid alcohols
Piotr Kopczacki, Maria Gumu ka, Marek Masnyk, Halina Grabarczyk,Gerard Nowak, W odzimierz M. Daniewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     [2aR,4aS,5S,7aS,8S(R),10R,10aS,10bR]dimethyl 5-benzyloxy-4-methyl-2a,4a,7a,8,9,10,10a,10b-octahydro-8,10-phenylmethylenedioxynaphto[1,8-bc:4,4a-c']difuran-5,10a-dicarboxylate
C32H34O9     ÏàËÆ¶È:55.5%
Tetrahedron          1995          51          2077-2090
Chemistry of insect antifeedants from Azadirachta Indica (part 18): Demethylation and methylation of the C-8 position of the decalin portion of azadirachtin
Wim-Jan Koot, Steven V. Ley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     N-((S)-2-tert-Butoxycarbonyl-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-L-valine methylester
    ÏàËÆ¶È:54.1%
Bioorganic & Medicinal Chemistry          2011          19          871-882
2-Substituted (S)-2-(3,3-dimethyl-1-oxo-10,10a-dihydroimidazo[1,5-b]isoquinolin-2(1H,3H,5H)-yl)acetic acids: Conformational prediction, synthesis,anti-thrombotic and vasodilative evaluation
Hong Wang, Le Peng, Ming Zhao , Jiawang Liu, Xiaoyi Zhang, Yuji Wang, Jianhui Wu, Li Li, Shiqi Peng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     cis-N-Benzyl-3-methoxy-3,4-dihydrospiro[[2]benzopyran-1,1'-cyclohexan]-4'-amine
    ÏàËÆ¶È:54.1%
Bioorganic & Medicinal Chemistry          2011          19          3141-3151
Design, synthesis and pharmacological evaluation of spirocyclic r1 receptor ligands with exocyclic amino moiety (increased distance 1)
Elisabeth Rack ,Roland Fröhlich, Dirk Schepmann , Bernhard W¨¹nsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Compound 7
C33H37N4O8     ÏàËÆ¶È:54.1%
Chemistry ¨C An Asian Journal          2011          6          3260-3269
Thermoresponsive Supramolecular Dendronized Polymers
Jiatao Yan, Wen Li, Kun Liu, Dalin Wu, Feng Chen, Peiyi Wu, and Afang Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     8-H©q2PF6
    ÏàËÆ¶È:54.1%
Organic letters          1999          1          129-132
Triphenylphosphonium-Stoppered [2]Rotaxanes
Stuart J. Rowan, Stuart J. Cantrill, and J. Fraser Stoddart
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     4-(12-azidododecyl)-4-benzyl-2-phenyl-1,3-oxazol-5(4H)-one
    ÏàËÆ¶È:54.1%
Heterocycles          2009          79          985-1005
Synthesis of Macrocyclic Lactams from 2-(¦Ø-Aminoalkyl)-2-benzoylamino-3-phenyl-N,N-dimethylpropanamides via Direct Amide Cyclization
Stephan P. Fritschi, Anthony Linden, and Heinz Heimgartner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     4-(11-azidoundecyl)-4-benzyl-2-phenyl-1,3-oxazol-5(4H)-one
    ÏàËÆ¶È:54.1%
Heterocycles          2009          79          985-1005
Synthesis of Macrocyclic Lactams from 2-(¦Ø-Aminoalkyl)-2-benzoylamino-3-phenyl-N,N-dimethylpropanamides via Direct Amide Cyclization
Stephan P. Fritschi, Anthony Linden, and Heinz Heimgartner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     4-(10-azidodecyl)-4-benzyl-2-phenyl-1,3-oxazol-5(4H)-one
    ÏàËÆ¶È:54.1%
Heterocycles          2009          79          985-1005
Synthesis of Macrocyclic Lactams from 2-(¦Ø-Aminoalkyl)-2-benzoylamino-3-phenyl-N,N-dimethylpropanamides via Direct Amide Cyclization
Stephan P. Fritschi, Anthony Linden, and Heinz Heimgartner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     compound 4
C25H30N2O8     ÏàËÆ¶È:54.1%
Heterocycles          2003          59          107-113
Toward the Assignment of Liposidomycin Stereochemistry: Synthesis of 1,4-Diazepan-3-One Analogues by Reductive Amination Approach
Noriyuki Nakajima,* Takahiro Isobe, Shiro Irisa, and Makoto Ubukata*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     (4aR,8aR)-2-benzenesulfonyl-8a-[(4R)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]meth-yl-1,2,3,4,4a,5,6,8a-octahydroisoquinoline-1,6-dione
C27H30O7N2S2     ÏàËÆ¶È:54.1%
Heterocycles          2003          59          721-733
Practical Synthesis of A 3,4,4a,5,8,8a-Hexahydro-2H-isoquinolin-1, 6-dione Ring System by the Diels-Alder Reaction of an Optically Active Dienophile, a 5, 6-Dihydro-1H-pyridin-2-one Derivative, with Siloxydiene
Masako Nakagawa,* Hideharu Uchida, Koji Ono, Yoshiyuki Kimura, Mariko Yamabe, Takeshi Watanabe, Riichiro Tsuji, Masakatsu Akiba, Yukiyoshi Terada, Dai Nagaki, Sachiko Ban, Naoki Miyashita, Takuya Kano, Chumpol Theeraladanon, Keisuke Hatakeyama, Mitsuhiro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     Pent-4-enyl 2-acetamido-4-O-acetyl-3,6-di-O-benzyi-2-deoxy-¦Â-D-glucopyranoside
C29H38NO7     ÏàËÆ¶È:54.1%
Bioorganic & Medicinal Chemistry          1996          4          1909-1918
N-tetrachlorophthaloyl (TCP) for ready protection/deprotection of amino sugar glycosides
John S Debenham, Sheryl D Debenham, Bert Fraser-Reid
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     4-Pentenyl 2-O-benzoyl-3-O-benzyl-6-(4-methoxybenzyl)-4-O-methyl-¦Á-D-mannopyranoside
C34H40O8     ÏàËÆ¶È:54.1%
Bioorganic & Medicinal Chemistry          1996          4          2011-2022
New synthetic trisaccharide inhibitors for N-acetylglucosaminyltransferase-V
Pu-Ping Lu, Ole Hindsgaul, Catharine A. Compston, Monica M. Palcic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     compound 3(n=2)
C45H49NO9     ÏàËÆ¶È:54.1%
Heterocycles          2002          58          393-403
Formation of Heterocyclic Derivatives of ¦Á-Amino Acids Using Vicinal Tricarbonyl Methodology
Harry H. Wasserman,* Yun Oliver Long, Rui Zhang, and Jonathan Parr
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     compound 6b
C34H42N2O10     ÏàËÆ¶È:54.1%
Heterocycles          2002          58          393-403
Formation of Heterocyclic Derivatives of ¦Á-Amino Acids Using Vicinal Tricarbonyl Methodology
Harry H. Wasserman,* Yun Oliver Long, Rui Zhang, and Jonathan Parr
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     N-(3S-N-boc-L-histidinyl-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-L-histidine benzylester
C34H39N7O6     ÏàËÆ¶È:54.1%
Bioorganic & Medicinal Chemistry          2010          18          1536-1554
2, 3-Diamino acid modifying 3S-tetrahydroisoquinoline-3-carboxylic acids: Leading to a class of novel agents with highly unfolded conformation, selective in vitro anti-platelet aggregation and potent in vivo anti-thrombotic activity
Xiaoyi Zhang, Wei Wang, Shenling Cheng, Ming Zhao, Meiqing Zheng, Heng Wei Chang, Jianhui Wu, Shiqi Peng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     bis-(R)-MPA ester of 6-[(1'S,2'S)-dihydroxypentyl]-2H-pyran-2-one
C28H30O8     ÏàËÆ¶È:54.1%
Tetrahedron          2009          65          4834-4840
Hemisynthesis and absolute configuration of novel 6-pentyl-2H-pyran-2-one derivatives from Trichoderma spp.
Mourad Daoubi, Cristina Pinedo-Rivilla, M. Bel¨¦n Rubio, Rosa Hermosa, Enrique Monte, Josefina Aleu, Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     bis-(S)-MPA ester of 6-[(1'R,2'R)-dihydroxypentyl]-2H-pyran-2-one
C28H30O8     ÏàËÆ¶È:54.1%
Tetrahedron          2009          65          4834-4840
Hemisynthesis and absolute configuration of novel 6-pentyl-2H-pyran-2-one derivatives from Trichoderma spp.
Mourad Daoubi, Cristina Pinedo-Rivilla, M. Bel¨¦n Rubio, Rosa Hermosa, Enrique Monte, Josefina Aleu, Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     6-[(1'S,2'S)-dihydroxypentyl]-2H-pyran-2-one bis-(R)-MPA ester
C28H30O8     ÏàËÆ¶È:54.1%
Tetrahedron          2009          65          4834-4840
Hemisynthesis and absolute configuration of novel 6-pentyl-2H-pyran-2-one derivatives from Trichoderma spp.
Mourad Daoubi, Cristina Pinedo-Rivilla, M. Bel¨¦n Rubio, Rosa Hermosa, Enrique Monte, Josefina Aleu, Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-05-14 18:27:27
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