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jinweiyang

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[ÇóÖú] ÇóÖú B-27µÄ½á¹¹ ÒÑÓÐ2È˲ÎÓë

13C NMR (101 MHz, CDCl3) ¦Ä
11.76,14.27,16.07,19.74,25.96,42.59,46.47,46.56,51.53,60.87,68.55,107.69,213.35
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jinweiyang: ½ð±Ò+6, ¡ïÓаïÖú 2014-12-16 21:37:39
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1 .     (1S*,2S*,5R*,6R*,8S*,9R*)-8-bromo-2,5,6,9-tetramethyltricyclo-[7.2.0.0(1,6)]undecane-3-one
C15H23OBr     ÏàËÆ¶È:60%
Tetrahedron          2002          58          6749-6755
Halogenated sesquiterpenes from the red alga Laurencia obtusa
Dimitra Iliopoulou, Vassilios Roussis, Christophe Pannecouque, Erik De Clercq, Constantinos Vagias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     diethyl (1,3,3-trimethylbicyclo[2.2.1]heptan-2-ylidene)methanephosphonate
    ÏàËÆ¶È:53.8%
Heterocycles          2007          72          541-552
Formation of Phosphonylated Thiiranes in the Reaction of a Diazomethanephosphonate and Cycloaliphatic Thioketones
Grzegorz Mloston, Katarzyna Urbaniak, Stanislaw Lesniak, Piotr Wasiak, and Heinz Heimgartner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (¡À)-N,N-Dipropyl [(N'-ethoxycarbonyl)piperidine]-2-car-boxamide
C15H28N2O3     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry          2000          8          591-600
Syntheses of R and S isomers of AF-DX 384, a selective antagonist of muscarinic M2 receptors
Juliette Martin, Annamaria Deagostino, C¨¦cile Perrio, François Dauphin, Christophe Ducandas, Christophe Morin, Paul-Louis Desb¨¨ne, Marie Claire Lasne
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     exo-Bornyl chloride
C10H17Cl     ÏàËÆ¶È:53.8%
Zeitschrift f¨¹r Naturforschung B          2009          64          25-40
Formation of Quaternary Stereogenic Centers by Wagner-Meerwein Rearrangement - Synthesis of Optically Active Cyclopentadienyl Complexes from Borneol and Fenchol
C. Färber, G. Wolmershäuser, and H. Sitzmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (1R*,5R*)-Ethyl 3-ethyl-9-oxo-3-azabicyclo[3.3.1]nonane-1-carboxylate
    ÏàËÆ¶È:53.8%
Tetrahedron          2012          68          1017-1028
An efficient synthesis of 3-alkyl-1,5,3-dioxazepanes and their use as electrophiles in double-Mannich reactions
Kevin Sparrow, David Barker, Margaret A. Brimble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     4¦Á-eudesmene-1¦Â,6¦Á-diol
C15H26O3     ÏàËÆ¶È:53.3%
Phytochemistry          2002          59          811-815
Sesquiterpenoids of Torilis japonica fruit
Junichi Kitajima, Nobuyuki Suzuki, Mituru Satoh, Mitsuo Watanabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     pulioplopanone B
C15H26O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2005          68          523-531
Sesquiterpenoids from Pulicaria canariensis and Their Cytotoxic Activities
Jorge Triana, Mariana Lpez, Francisco J. Prez, Javier Gonzlez-Platas,Jos Quintana, Francisco Estvez, Francisco Len, and Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     methyl 2¦Á-hydroxy-6-oxo-11-pinguisanoate
CI6H26O4     ÏàËÆ¶È:50%
Phytochemistry          1996          43          1249-1253
Pinguisane and sacculatane terpenoids from the liverwort Porella platyphylla
Malcolm S. Buchanan, Joseph D. Connolly, David S. Rycroft
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     5-oxo-5.6H-silphiperfolen
    ÏàËÆ¶È:50%
Phytochemistry          1980          19          579-582
Neue sesquiterpene aus Liabum-arten
Ferdinand Bohlmann, Christa Zdero, Rolf Bohlmann, Robert M. King, Harold Robinson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     5,9,10-trimethyl-4-oxahexacyclo[5.4.1.0(2,6).0(3,10).0(5,9).0(8,11)]dodecan-3-ol
C14H18O2     ÏàËÆ¶È:50%
Heterocycles          2000          52          451-457
Reactions of Cage-annulated 2-Methyl-5-(trifluoromethanesulfonyloxy)furans with Lithium Diisopropylamide. Evidence for Nucleophilic Reactivity of LDA
Alan P. Marchand* and Irishi Narayanan Narayanan Namboothiri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     methyl 7¦Á-hydroxy-13-oxopodocarpan-18-oate
    ÏàËÆ¶È:50%
Magnetic Resonance in Chemistry          1990          28          529-532
13C nuclear magnetic resonance spectra of several podocarpane and cassane diterpenoids
A. Abad, C. Agull¨®, M. Arn¨®, L. R. Domingo and R. J. Zaragoz¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound 26
    ÏàËÆ¶È:50%
Magnetic Resonance in Chemistry          1992          30          183-185
13C NMR chemical shift assignments for substituted 2-azabicyclo[3.3.1] nonan-7-ones
N¨²ria Casamitjana, Josep Bonjoch, Jordi Gr¨¤cia and Joan Bosch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     1-O-[(tert-butyl)diphenylsilyl]-2,4-dideoxy-2-ethyl-4-methyl-l-arabinitol
C24H36O3Si     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2014          97          868-880
Olefin Cross-Metathesis: Studies towards the Total Synthesis of (+)-Bitungolide F
Gandrath Dayaker and Palakodety Radha Krishna
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2014-12-15 23:12:28
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seuseasoar

ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

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1 .     colomitide A
C13H22O3     ÏàËÆ¶È:100%
Chemistry & Biodiversity          2009          6          1216-1223
Colomitides A and B: Novel Ketals with an Unusual 2,7-Dioxabicyclo[3.2.1]octane Ring System from the Aquatic Fungus YMF 1.01029
Jin-Yan Dong, Li-Mei Wang, Hong-Chuang Song, Kai-Ze Shen, Yong-Ping Zhou, Le Wang, and Ke-Qin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (1S*,2S*,5R*,6R*,8S*,9R*)-8-bromo-2,5,6,9-tetramethyltricyclo-[7.2.0.0(1,6)]undecane-3-one
C15H23OBr     ÏàËÆ¶È:60%
Tetrahedron          2002          58          6749-6755
Halogenated sesquiterpenes from the red alga Laurencia obtusa
Dimitra Iliopoulou, Vassilios Roussis, Christophe Pannecouque, Erik De Clercq, Constantinos Vagias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     diethyl (1,3,3-trimethylbicyclo[2.2.1]heptan-2-ylidene)methanephosphonate
    ÏàËÆ¶È:53.8%
Heterocycles          2007          72          541-552
Formation of Phosphonylated Thiiranes in the Reaction of a Diazomethanephosphonate and Cycloaliphatic Thioketones
Grzegorz Mloston, Katarzyna Urbaniak, Stanislaw Lesniak, Piotr Wasiak, and Heinz Heimgartner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (¡À)-N,N-Dipropyl [(N'-ethoxycarbonyl)piperidine]-2-car-boxamide
C15H28N2O3     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry          2000          8          591-600
Syntheses of R and S isomers of AF-DX 384, a selective antagonist of muscarinic M2 receptors
Juliette Martin, Annamaria Deagostino, C¨¦cile Perrio, François Dauphin, Christophe Ducandas, Christophe Morin, Paul-Louis Desb¨¨ne, Marie Claire Lasne
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     exo-Bornyl chloride
C10H17Cl     ÏàËÆ¶È:53.8%
Zeitschrift f¨¹r Naturforschung B          2009          64          25-40
Formation of Quaternary Stereogenic Centers by Wagner-Meerwein Rearrangement - Synthesis of Optically Active Cyclopentadienyl Complexes from Borneol and Fenchol
C. Färber, G. Wolmershäuser, and H. Sitzmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (1R*,5R*)-Ethyl 3-ethyl-9-oxo-3-azabicyclo[3.3.1]nonane-1-carboxylate
    ÏàËÆ¶È:53.8%
Tetrahedron          2012          68          1017-1028
An efficient synthesis of 3-alkyl-1,5,3-dioxazepanes and their use as electrophiles in double-Mannich reactions
Kevin Sparrow, David Barker, Margaret A. Brimble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Methyl 4-(bromomethyl)-7,7-dimethyl-2,3-dioxobicyclo[2.2.1] heptane-1-carboxylate
C12H15BrO4     ÏàËÆ¶È:53.8%
Tetrahedron          2012          68          1972-1978
A route to a wide range of cyclopentanecarboxylic acids via 4-substituted camphors
Volodymyr O. Knizhnikov, Zoya V. Voitenko, Vladimir B. Golovko, Marian V. Gorichko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     4¦Á-eudesmene-1¦Â,6¦Á-diol
C15H26O3     ÏàËÆ¶È:53.3%
Phytochemistry          2002          59          811-815
Sesquiterpenoids of Torilis japonica fruit
Junichi Kitajima, Nobuyuki Suzuki, Mituru Satoh, Mitsuo Watanabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     pulioplopanone B
C15H26O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2005          68          523-531
Sesquiterpenoids from Pulicaria canariensis and Their Cytotoxic Activities
Jorge Triana, Mariana Lpez, Francisco J. Prez, Javier Gonzlez-Platas,Jos Quintana, Francisco Estvez, Francisco Len, and Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     cytochalasin N
C30H39NO5     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1987          35          902-905
THREE NEW 10-PHENYL- [11] CYTOCHALASANS, CYTOCHALASINS N, O, AND P FROM PHOMOPSIS SP
Takako Tomioka,Yoshihiko Izawa,Kiyotaka Koyama and Shinsaku Natori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     methyl 2¦Á-hydroxy-6-oxo-11-pinguisanoate
CI6H26O4     ÏàËÆ¶È:50%
Phytochemistry          1996          43          1249-1253
Pinguisane and sacculatane terpenoids from the liverwort Porella platyphylla
Malcolm S. Buchanan, Joseph D. Connolly, David S. Rycroft
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     5-oxo-5.6H-silphiperfolen
    ÏàËÆ¶È:50%
Phytochemistry          1980          19          579-582
Neue sesquiterpene aus Liabum-arten
Ferdinand Bohlmann, Christa Zdero, Rolf Bohlmann, Robert M. King, Harold Robinson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     5,9,10-trimethyl-4-oxahexacyclo[5.4.1.0(2,6).0(3,10).0(5,9).0(8,11)]dodecan-3-ol
C14H18O2     ÏàËÆ¶È:50%
Heterocycles          2000          52          451-457
Reactions of Cage-annulated 2-Methyl-5-(trifluoromethanesulfonyloxy)furans with Lithium Diisopropylamide. Evidence for Nucleophilic Reactivity of LDA
Alan P. Marchand* and Irishi Narayanan Narayanan Namboothiri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     methyl 7¦Á-hydroxy-13-oxopodocarpan-18-oate
    ÏàËÆ¶È:50%
Magnetic Resonance in Chemistry          1990          28          529-532
13C nuclear magnetic resonance spectra of several podocarpane and cassane diterpenoids
A. Abad, C. Agull¨®, M. Arn¨®, L. R. Domingo and R. J. Zaragoz¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     compound 26
    ÏàËÆ¶È:50%
Magnetic Resonance in Chemistry          1992          30          183-185
13C NMR chemical shift assignments for substituted 2-azabicyclo[3.3.1] nonan-7-ones
N¨²ria Casamitjana, Josep Bonjoch, Jordi Gr¨¤cia and Joan Bosch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     1-O-[(tert-butyl)diphenylsilyl]-2,4-dideoxy-2-ethyl-4-methyl-l-arabinitol
C24H36O3Si     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2014          97          868-880
Olefin Cross-Metathesis: Studies towards the Total Synthesis of (+)-Bitungolide F
Gandrath Dayaker and Palakodety Radha Krishna
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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3Â¥2014-12-15 23:12:28
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