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1 .     1,2,3,6-tetra-O-acetyl-5-deoxy-¦Á,¦Â-L-arabino-hexofuranose(¦Â-anomer)
C14H20O9     ÏàËÆ¶È:61.5%
Bioorganic & Medicinal Chemistry          2010          18          5339-5345
Synthesis of 5-deoxy-¦Â-d-galactofuranosides as tools for the characterization of ¦Â-d-galactofuranosidases
Andrea Bordoni, Rosa M. de Lederkremer, Carla Marino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     1¦Â,6¦Á,8¦Â-trihydroxy-11,13-dihydroeudesm-4-en-6-olide 8-acetate
C17H24O5     ÏàËÆ¶È:58.8%
Phytochemistry          1990          29          1689-1690
Eudesmanolides from Stevia aff. tomentosum
Mariano Mart¨ªnez-Vazquez,Rosa Elena Gallegos,Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     1-C-(R-Propan-2'-ol)-3,5-di-O-acetyl-2,2'-anhydro-¦Á-D-ribofuranoside
    ÏàËÆ¶È:58.3%
Canadian Journal of Chemistry          2006          84          597-602
Stereoselective synthesis of dioxabicycles from 1-C-allyl-2-O-benzyl-glycosides - An intramolecular cyclization between 2-O-benzyl oxygen and the allyl double bond1
An-Tai Wu, Tian Yi, Huawu Shao, Shih-Hsiung Wu, and Wei Zou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (-)-p-menthanetriol
    ÏàËÆ¶È:58.3%
Bioscience, Biotechnology, and Biochemistry          2003          67          475-479
(+)-Menthol and Its Hydroxy Derivatives, Novel Fungal Monoterpenols from the Fusicoccin-producing Fungi, Phomopsis amygdali F6a and Niigata 2
Takeshi SASSA, Hiromichi KENMOKU, Mitsuyoshi SATO, Tetsuya MURAYAMA and Nobuo KATO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 52
C19H37O4ISi     ÏàËÆ¶È:58.3%
Tetrahedron          2013          69          7746-7758
Stereoselectivity of electrophile-promoted oxacyclizations of 1,4-dihydroxy-5-alkenes to 3-hydroxytetrahydropyrans
Frank E. McDonald, Kento Ishida, Jessica A. Hurtak
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 2
    ÏàËÆ¶È:58.3%
Magnetic Resonance in Chemistry          1990          28          659-660
1H and 13C NMR study of the neomenthyl halides: A very high field proton shift in the iodide
Gordon L. Lange and Christine Gottardo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     pericyclocamphanone
    ÏàËÆ¶È:58.3%
Organic Magnetic Resonance          1973          5          277-283
Carbon-13 chemical shifts of substituted nortricyclenes
E. Lippmaa, T. Pehk and J. Paasivirta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (1¦Á,4a¦Â,8a¦Â)-4a-methyldecahydronaphthalene-1,8a-diol
    ÏàËÆ¶È:58.3%
Australian Journal of Chemistry          1981          34          1451-1465
Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols
JM Coxon and JR Gibson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (4a¦Á,5¦Â,8a¦Á)-5-acetoxy-8a-methyldecahydronaphthalen-4a-ol
    ÏàËÆ¶È:58.3%
Australian Journal of Chemistry          1981          34          1451-1465
Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols
JM Coxon and JR Gibson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     [3-(N-Acetyl-N-methyl-amino)-propyl]-phosphonic acid
    ÏàËÆ¶È:58.3%
Bioorganic & Medicinal Chemistry          2006          14          2375-2385
Evaluation of fosmidomycin analogs as inhibitors of the Synechocystis sp. PCC6803 1-deoxy-d-xylulose 5-phosphate reductoisomerase
Youn-Hi Woo, Roberta P.M. Fernandes, Philip J. Proteau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     1¦Â,4¦Â,5¦Á-trihydroxy-6¦Â-acetoxyeudesmane
C17H30O5     ÏàËÆ¶È:56.2%
Journal of Natural Products          1988          Vol 51          475
Epoxidation Reaction of 6¦Â-Acetoxyeudesmenes and Acid-catalyzed Transformations of the Epoxy Compounds
E. Cabrera, A. Garcia-Granados, M. A. Quecuty
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     jioglutin C triacetae
C16H22O9     ÏàËÆ¶È:56.2%
Phytochemistry          1989          28          2385-2391
Five cyclopentanoid monoterpenes from Rehmannia glutinosa
Takashi Morota,Hiroaki Nishimura,Hiroshi Sasaki,Masao Chin (Chen Zhengxiong),Kô Sugama,Takao Katsuhara,Hiroshi Mitsuhashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (E and Z)-N-[(1R*,2R*)-2-Chloro-1,3-dimethylbutyl]-N'-[(4-methylphenyl)sulfonyl]ethanimidamide
C15H23ClN2O2S     ÏàËÆ¶È:53.8%
Helvetica Chimica Acta          2010          93          233-241
Copper-Catalyzed Ritter-Type Reaction of Unactivated Alkenes with Dichloramine-T
Takumi Abe, Hiroyuki Takeda, Yoshihisa Miwa, Koji Yamada, Reiko Yanada and Minoru Ishikura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     2-(2,4,6-trimethyl-phenyl)-tetrahydro-pyrazolo[1,2-a]pyridazine-1,3-dione
C16H20N2O2     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry          2009          17          4241-4256
Aryldiones incorporating a [1,4,5]oxadiazepane ring. Part I: Discovery of the novel cereal herbicide pinoxaden
Michel Muehlebach, Manfred Boeger, Fredrik Cederbaum, Derek Cornes, Adrian A. Friedmann, Jutta Glock, Thierry Niderman, Andr¨¦ Stoller, Trixie Wagner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     hippodamine
    ÏàËÆ¶È:53.8%
Magnetic Resonance in Chemistry          1999          37          60-64
Complete assignment of the 1H and 13C NMR spectra of the Coccinellidae-defensive alkaloids myrrhine, precoccinelline and hippodamine, their N -oxides and the corresponding hydrochlorides
B. Lebrun, J. C. Braekman and D. Daloze
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (¡À)-(4aS,8aR)-2,5,5,8a-Tetramethyl-cis-4a,5,6,7,8,8ahexahydro-4H-1-benzopyran
    ÏàËÆ¶È:53.8%
Flavour and Fragrance Journal          2006          21          659-666
Synthesis and odour evaluation of stereoisomers of octahydrobenzopyran derivatives
Pablo J. Linares-Palomino, Sof¨ªa Salido, Joaqu¨ªn Altarejos, Manuel Nogueras and Adolfo S¨¢nchez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     2-(c-3-Acetoxy-1,2,2-trimethyl-r-1-cyclopentyl)propanedinitrle
C13H18N2O2     ÏàËÆ¶È:53.8%
Helvetica Chimica Acta          1995          78          2065-2076
Cascade Cyclizations of Terpenoid Polyalkenes Triggered by Photoelectron Transfer ¨C Biomimetics with Photons
Klaus-Dieter Warzecha, Xuechao Xing, Martin Demuth, Richard Goddard, Magnus Kessler and Carl Kr¨¹ger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     compound 22b
    ÏàËÆ¶È:53.8%
Magnetic Resonance in Chemistry          1994          32          732-738
13C NMR of 4,5-epoxy-3-substituted decalin and analogous ¦¤4-octalin derivatives: Epoxide- and methyl-induced shifts
Adrian Martin Pohlit and Helena Maria Carvalho Ferraz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     4¦Â,7¦Â,11-enantioeudesmantriol
C15H28O3     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2007          55(3)          376-381
Two Minor Diterpene Glycosides and an Eudesman Sesquiterpene from Coleus forskohlii
Yupei SHAN,Xiaobing WANG,Xiang ZHOU,Lingyi KONG,and Masatake NIWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     chrysothol
C15H26O2     ÏàËÆ¶È:53.3%
Phytochemistry          2006          67          1547-1553
Constituents of Chrysothamnus viscidiflorus
Ahmed A. Ahmed , Mohamed-Elamir F. Hegazy, Nahed M. Hassan,Malgorzata Wojcinska, Joe Karchesy, Paul W. Pare, Tom J. Mabry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     4¦Â-hydroxy-4, 10¦Á-dimethyl-7¦ÁH,8¦ÁH-eudesman-11-ene-8,12-olide
C15H22O3     ÏàËÆ¶È:53.3%
Phytochemistry          2004          65          2039-2043
Constituents of two Flourensia species
Mar¨ªa L. Uriburu, Juana R. de la Fuente, Jorge Palermo, Roberto R. Gil,Virginia E. Sosa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (-)-7¦ÂH-eudesmane-4¦Á,11-diol
C15H28O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1998          61          22-28
Enantioselective Total Syntheses of (-)-7¦ÂH-Eudesmane-4¦Á, 11-diol and (+)-ent-7¦ÂH-Eudesmane-4¦Á, 11-diol
Fumito Shimoma, Hisao Kondo, Saori Yuuya, Toshio Suzuki, Hisahiro Hagiwara, and Masayoshi Ando
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     Buchariol
C15H26 O2     ÏàËÆ¶È:53.3%
Molecules          2005          10          971-977
Terpenoids from Cleome droserifolia (Forssk.) Del
Hesham I. El-Askary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Pterodondiol
    ÏàËÆ¶È:53.3%
Journal of Asian Natural Products Research          2007          9          277-283
Sesquiterpenoids from Hedychium yunnanense and Porana discifera, and the structural revision of two sesquiterpenoids from Laggera pterodonta
W.-M. ZHU, Q. ZHAO, S.-L. LI and X.-J. HAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     4,5-epi-cryptomeridiol
C15H26O     ÏàËÆ¶È:53.3%
Journal of Natural Products          1992          Vol 55          730
Three New Eudesmane Sesquiterpenes from Pluchea arguta
Viqar Uddin Ahmad, Tanveer Ahmed Farooqui, Kaniz Fizza, Azra Sultana, Rasheeda Khatoon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     4,5-epi-cryptomeridiol
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1994          Vol 57          1189
Synthetic Studies of Sesquiterpenes with a cis-Fused Decalin System, 4. Synthesis of (+)-5¦ÂH-Eudesma-3,11-diene, (-)-5¦ÂH-Eudesmane-4¦Â,11-diol, and (+)-5¦ÂH-Eudesmane-4¦Á,11-diol, and Structure Revision of a Natural Eudesmane-4,11-diol Isolated from Pluchea
Masayoshi Ando, Koji Arai, Kazuhira Kikuchi, Koji Isogai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     4¦Â,11-dihydroxy-10-epi-eudesmane
C15H26O     ÏàËÆ¶È:53.3%
Phytochemistry          1992          31          863-880
Sesquiterpene lactones and other constituents from Ursinia species
J. Jakupovic, U. Ganzer, P. Pritschow, L. Lehmann, F. Bohlmann, R.M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     4¦Â,11-¶þôÇ»ù-¶ÔÓ³èñÍé
C15H28O2     ÏàËÆ¶È:53.3%
Chinese Pharmaceutical Journal          1995          30          264-265
Chemical study on Laggera pterodonta
Zhao Aihua, Zhu Yan, Wei Junxian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     compound X
    ÏàËÆ¶È:53.3%
Heterocycles          2001          54          765-776
Intramolecular Photocycloaddition of 2-Cycloalkenyl-1,3-dioxin-4-one. Stereoselective Synthesis of cis-Eudesmane-4,11-diols
Toshihide Hatsui,* Ka Li, Akira Mori,* and Hitoshi Takeshita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     7-methoxy-1,7-dimethyltricyclo[6.2.2.0(4,9)]dodecan-3-one
C15H24O2     ÏàËÆ¶È:53.3%
European Journal of Organic Chemistry          2006          2006          3181-3192
Towards the Total Synthesis of Vibsanin E, 15-O-Methylcyclovibsanin B,3-Hydroxyvibsanin E, Furanovibsanin A, and 3-O-Methylfuranovibsanin A
Brett D. Schwartz, David P. Tilly, Ralf Heim, Stefan Wiedemann, Craig M. Williams and Paul V. Bernhardt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     4,10-epoxy-6¦Á-hydroxyguaiane
    ÏàËÆ¶È:53.3%
Zeitschrift f¨¹r Naturforschung C          2012          67          266-274
Isolation of New Cytotoxic Metabolites from Cleome droserifolia Growing in Egypt
Shahira M. Ezzat and Amira Abdel Motaal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     compound 8
    ÏàËÆ¶È:53.3%
The Journal of Organic Chemistry          1983          48          4410-4413
An aristolane sesquiterpenoid from the sea pen Scytalium splendens
Muu N. Do, Karen L. Erickson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     pterodondiol
C15H28O2     ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          2014          50          732-734
Chemical Components of the Fibrous Root of Ophiopogon japonicus
Tian Feng, Shen Lan, Wang ChenJie, Feng Yi, Zheng XiangWei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     chrysothol monoacetyl derivative(1b)
    ÏàËÆ¶È:52.9%
Phytochemistry          2006          67          1547-1553
Constituents of Chrysothamnus viscidiflorus
Ahmed A. Ahmed , Mohamed-Elamir F. Hegazy, Nahed M. Hassan,Malgorzata Wojcinska, Joe Karchesy, Paul W. Pare, Tom J. Mabry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     rel- (1R,2R,3R,4S,6S)-p-menthane-1,2,3,6-tetrol
C10H20O4     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2006          Vol. 89          558
Terpenoids from Eupatorium fortunei TURCZ
Hai-Xia Jiang, Ya Li, Jing Pan, and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     (1R,2R)-p-menth-3-ene-1,2-diol
C10H18O2     ÏàËÆ¶È:50%
Phytochemistry          2004          65          3279-3287
Monoterpenoids and their glycosides from the leaf of thyme
Junichi Kitajima, Toru Ishikawa, Atushi Urabe, Mitsuru Satoh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     pandangolide 1a
C12H20O5     ÏàËÆ¶È:50%
Journal of Natural Products          2005          68          1350-1353
Pandangolide 1a, a Metabolite of the Sponge-Associated Fungus Cladosporium sp., and the Absolute Stereochemistry of Pandangolide 1 and iso-Cladospolide B
Shiri Gesner, Naama Cohen, Micha Ilan, Oded Yarden, and Shmuel Carmeli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     pandangolide 1
C12H20O5     ÏàËÆ¶È:50%
Journal of Natural Products          2005          68          1350-1353
Pandangolide 1a, a Metabolite of the Sponge-Associated Fungus Cladosporium sp., and the Absolute Stereochemistry of Pandangolide 1 and iso-Cladospolide B
Shiri Gesner, Naama Cohen, Micha Ilan, Oded Yarden, and Shmuel Carmeli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     pandangolide 4
C24H38O8S     ÏàËÆ¶È:50%
Journal of Natural Products          2001          64          527-530
New Macrolides and Furan Carboxylic Acid Derivative from the Sponge-Derived Fungus Cladosporium herbarum
Raquel Jadulco,Peter Proksch,Victor Wray,Sudarsono,Albrecht Berg,and Udo Gräfe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     3-isopropyl-6-methyltricyclo[4.4.0.02,8]decan-7-one
    ÏàËÆ¶È:50%
Journal of Natural Products          2001          64          406-410
A Formal Total Synthesis of Racemic Sesquiterpenoid Sativene
Sasan Karimi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     pandangolide 1
C12H21O5     ÏàËÆ¶È:50%
Journal of Natural Products          2000          63          142-145
Novel Polyketide Metabolites from a Species of Marine Fungi
Cameron J. Smith,Darren Abbanat, Valerie S. Bernan, William M. Maiese, Michael Greenstein, Jamaluddin Jompa,Akbar Tahir,and Chris M. Ireland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     cis-4,8-dimethyl-6-nonanolide
C11H20O2     ÏàËÆ¶È:50%
Journal of Natural Products          1997          60          493-494
A Synthesis of 6-Myoporol
Tse-Lok Ho and Rong-Jie Chein
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     cytochalasin P
C30H41NO6     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
44 .     (R)-6-[(acetyloxy)imino]-4-methyl-1-isopropylcyclohex-1-ene
C12H19NO2     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2003          39          569-572
(R)-4-MENTHEN-3-ONE anti-OXIME AND ITS TRANSFORMATION UNDER BECKMAN REARRANGEMENT CONDITIONS
R. Ya. Kharisov, E. R. Latypova, R. F. Talipov,R. R. Muslukhov, G. Yu. Ishmuratov,and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     (1S*,2S*,3S*,4R*,6R*)-1,2,3,6-tetrahydroxy-P-menthane
C10H19O4     ÏàËÆ¶È:50%
Chinese Chemical Letters          2005          16          1217-1219
Highly Oxygenated Monoterpenes from Eupatorium fortunei
Hal Xia¢òANG Kun GAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     deoxyoleanolic acid
    ÏàËÆ¶È:50%
China Journal of Chinese Materia Medica          1989          14          32-33
Studies on the Chemical Constituents of Schizonepeta mulifida(L.)Briq
Zang Youwei, Ma Bingru
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     (E )-7¦ÁH-germacra-1(10),4(15)-diene-5¦Á,6¦Â-diol
C15H26O2     ÏàËÆ¶È:50%
Phytochemistry          1999          51          529-541
Bioactive sesquiterpenes from Santolina rosmarinifolia subsp. Canescens. A conformational analysis of the germacrane ring
Alejandro F. Barrero, M. Mar Herrador, Jose F.Quilez, Ramon Alvarez-Manzaneda, Dolores Portal, Jose A. Gavin, Dolores G. Gravalos, M.S.J. Simmonds, W.M. Blaney
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     1-hydroxy-2,2,6-trimethylbicyclo[4.2.2]dec-9-en-7-on
    ÏàËÆ¶È:50%
Helvetica Chimica Acta          1976          59          1-13
Die Thermolyse von 2,2,6,7-Tetramethyl-1,7-epidioxybicyclo[4.3.O]non-8-en
von Werner Skorianetz und Gunther Ohloff
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     2-Methyl-2-(5,5-dimethyl-2-oxo-1,3,2-dioxaphosphinan-2-yl)pyrrolidine
C10H20NO3P     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          2218-2230
CyDEPMPOs: A class of stable cyclic DEPMPO derivatives with improved properties as mechanistic markers of stereoselective hydroxyl radical adduct formation in biological systems
Gaëlle Gosset, Jean-Louis Cl¨¦ment, Marcel Culcasi, Antal Rockenbauer, Sylvia Pietri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     2-Methyl-2-(5,5-diethyl-2-oxo-1,3,2-dioxaphosphinan-2-yl)-3,4-dihydro-2H-pyrrole 1-oxide [Et2CyDEPMPO]
C12H22NO4P     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          2218-2230
CyDEPMPOs: A class of stable cyclic DEPMPO derivatives with improved properties as mechanistic markers of stereoselective hydroxyl radical adduct formation in biological systems
Gaëlle Gosset, Jean-Louis Cl¨¦ment, Marcel Culcasi, Antal Rockenbauer, Sylvia Pietri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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4Â¥2014-12-22 17:43:37
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