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23.39, 23.91, 24.99, 26.78, 27.10, 27.36, 27.47, 27.74, 44.16, 72.61, 129.84, 141.96, 174.95
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orbring: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-01-27 12:04:31
1 .     7-Carboxyl-8-carveol
    ÏàËÆ¶È:69.2%
Natural Product Research and Development          2014          26          1207-1211
Chemical Constituents from the Fruits of Dipteronia dyeriana
SHI Ya-na, LIU Da-hui, JIN Hang, YANG Yan, ZHAO Da-ke, WANG Yue-hu, LONG Chun-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 29
C16H30O4     ÏàËÆ¶È:62.5%
Heterocycles          2008          76          1313-1328
2, 6-Dimethyl-4-nitrobenzoic Anhydride (DMNBA): An Effective Coupling Reagent for the Synthesis of Carboxylic Esters and Lactones
Isamu Shiina and Ryo Miyao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (5Z,9Z)-14-methyl-5,9-pentadecadienoic acid
C16H28O2     ÏàËÆ¶È:61.5%
Journal of Natural Products          1997          60          502-504
Identification of the Novel Antimicrobial Fatty Acid (5Z, 9Z)-14-Methyl-5, 9-pentadecadienoic Acid in Eunicea succinea
N¨¦stor M. Carballeira, Elba D. Reyes, Anthony Sostre, Abimael D. Rodr¨ªguez, Jorge L. Rodr¨ªguez, and Fernando A. Gonz¨¢ lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     »·Ê®ÈýÄÚõ¥
    ÏàËÆ¶È:61.5%
Chemical Journal of Chinese Universities          2007          28          897-899
A New Method for Synthesis of Mcrocyclic Lactones via Malania Olceifera Chum Oil
LIU Xiong-M in, LI Wei-Guang, LI Piao-Ying, ZHOU Yong0Hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     6,7,8,9,10,11,12,13-octahydro-5H-cycloundeca[d]pyrimidine
C13H20N2     ÏàËÆ¶È:61.5%
Heterocycles          2006          70          581-586
One-Step Syntesis of 4,5-Disubstituted Pyrimidines Using Commercially Available and Inexpensive Reagents
Phil S. Baran,* Ryan A. Shenvi, and Steven A. Nguyen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     N1-(3-aminopropyl)-N3-cyclopentadecylpropane-1,3-diamine
C21H45N3     ÏàËÆ¶È:61.5%
Journal of Medicinal Chemistry          2014          57          4023-4034
Synthesis and Biological Evaluation of Antimetastatic Agents Predicated upon Dihydromotuporamine C and Its Carbocyclic Derivatives
Aaron Muth, Veethika Pandey, Navneet Kaur, Melissa Wason, Cheryl Baker, Xianlin Han, Teresa R. Johnson, Deborah A. Altomare, and Otto Phanstiel, IV
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     4,5,6,7,8,9,10,11,12,13-Decahydro-2-[(2H3)methyl]-1H-cyclopenta[12]annulene (
    ÏàËÆ¶È:60%
Helvetica Chimica Acta          2009          92          1782-1799
Synthesis of Deuterium-Labeled Perfume Ingredients as Internal Standards for Their GC/MS Quantification
Christian Chapuis, Carole Cantatore, Peter Fankhauser, Ren¨¦ Challand, Jean-Jacques Riedhauser
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     methyl 2-(2-ethylidenecyclooctyl)-3-methoxypropionate
C15H26O3     ÏàËÆ¶È:60%
Zeitschrift f¨¹r Naturforschung B          2001          56          1227-1234
Facile Approach to ersatile Chiral Intermediates for Fused Cyclopentanoid Natural Products
F. Zulfiqar and A. Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     1-ethylcyclotridec-1-ene
C15H28     ÏàËÆ¶È:57.1%
Russian Journal of Organic Chemistry          2010          46          807-811
RegioselectiveintermolecularcycloaluminationofcyclicallenesandethylenewithRnAlCl3−n,catalyzedbytitaniumandzirconiumcomplexes
V. A. D¡¯yakonov, R. K. Timerkhanov and U. M. Dzhemilev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     1-[(2-2H)ethyl](13-2H)cyclotridec-1-ene
C15H26D2     ÏàËÆ¶È:57.1%
Russian Journal of Organic Chemistry          2010          46          807-811
RegioselectiveintermolecularcycloaluminationofcyclicallenesandethylenewithRnAlCl3−n,catalyzedbytitaniumandzirconiumcomplexes
V. A. D¡¯yakonov, R. K. Timerkhanov and U. M. Dzhemilev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     2-[(1-methylamino)phenylmethyl]cyclooctane-1-thiol hydrochloride
C16H25NS     ÏàËÆ¶È:57.1%
Tetrahedron          2012          68          9016-9022
Facile access to ¦Ã-aminothiols from 1,3-thiazines via a microwave-assisted three-component reaction
Flavie Peudru, Remi Legay, Jean-François Lohier, Vincent Reboul, Mihaela Gulea
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     1,3-bis-(6-carboxypentyl)-4-pentylimidazolium
C20H34N2O4     ÏàËÆ¶È:57.1%
Chemical Research in Toxicology          2003          16          232-241
Model Studies on the Modification of Proteins by Lipoxidation-Derived 2-Hydroxyaldehydes
Zhongfa Liu and Lawrence M. Sayre
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     oxacyclopentadecan-2-one
C14H26O2     ÏàËÆ¶È:57.1%
Flavour and Fragrance Journal          2012          27          75-76
Isolation and identification of oxacyclopentadecan-2-one from the dried fruiting body of Dictyophora echinovolvata Zang, Zheng et Hu
Mingquan Huang, Hongyu Tian, Baoguo Sun and Yuping Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     maninsigin C
C16H28O2     ÏàËÆ¶È:56.2%
Fitoterapia          2013          84          58-63
Bioactive phenolics and terpenoids from Manglietia insignis
Shan-Zhai Shang, Ling-Mei Kong, Li-Ping Yang, Jing Jiang, Jin Huang, Hai-Bo Zhang, Yi-Ming Shi, Wei Zhao, Hong-Lin Li, Huai-Rong Luo, Yan Li, Wei-Lie Xiao, Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3-Chloro-3-Methylcyclopentadecan-1-one
C16H29OCl     ÏàËÆ¶È:56.2%
Flavour and Fragrance Journal          2012          27          54-59
Expedient synthesis of (E)-3-methylcyclopentadec-2-en-1-one, an important precursor for (R)-(−muscones
Hisahiro Hagiwara, Teppei Adachi, Masaharu Doya, Takashi Hoshi and Toshio Suzuki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 8
C18H28O4     ÏàËÆ¶È:55.5%
Journal of Natural Products          2003          66          1318-1323
Novel Oxylipin Metabolites from the Brown Alga Eisenia bicyclis
Kenji Kousaka, Nobuyuki Ogi, Yasutomo Akazawa,Makiko Fujieda, Yuzo Yamamoto, Yuuki Takada, and Junji Kimura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound 6a
C17H21N3O     ÏàËÆ¶È:53.8%
Chemical & Pharmaceutical Bulletin          1987          35          2646-2655
Highly Regioselective Synthesis of Trisubstituted Pyrrolidines by 1, 3-Cycloaddition
NOBUYUKI IMAI and KAZUO ACHIWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     7-acetoxy-p-menth-1-en-8-ol
    ÏàËÆ¶È:53.8%
Biochemical Systematics and Ecology          1995          23          875-876
Grilactone and other Terpenoids from Anthriscus nitida
Bernard Muckensturm, Fouzia Diyani, Jean-Pierre Reduron
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     compound Ia
    ÏàËÆ¶È:53.8%
Acta Pharmaceutica Sinica          1992          27          752-757
NEW MONOTERPENOIDS FROM CYNANCHUM HANCOCKIANUM
HX Lou; X Li; TR Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     7-hydroxyterpineol
C10H16O     ÏàËÆ¶È:53.8%
Phytochemistry          1991          30          583-587
Sesquiterpene lactones and other constituents from Artemisia xerophytica
R. X. Tan, J. Jakupovic, F. Bohlmann, Z. J. Jia, S. Huneck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     bicyclo[2.2.2]octane(g)
    ÏàËÆ¶È:53.8%
Helvetica Chimica Acta          1976          59          2437-2442
13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids
Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     oleuropeic acid methylester
    ÏàËÆ¶È:53.8%
Planta Medica          1994          60          467-469
Monoterpene Glucosides from Cunila spicata
Manns, D.; Hartmann, R.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     1,4-Dioxaspiro[4.15]icosane
    ÏàËÆ¶È:53.8%
Helvetica Chimica Acta          2012          95          428-447
Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone
Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     cis-(Z)-oxacyclotridec-10-en-2-one
    ÏàËÆ¶È:53.8%
Phytochemistry          1989          28          3311-3315
(Z)-oxacyclotridec-10-en-2-one,an alfalfa weevil feeding deterrent from Medicago rugosa
Robert P. Doss,Steven J. Gould,Kathleen J.R. Johnson,Robert A. Flath,Rodger L. Kohnert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     Compound 4a
    ÏàËÆ¶È:53.8%
Magnetic Resonance in Chemistry          2001          39          222-224
1H and 13C NMR spectral assignments for 3, 5-disubstituted tetrahydro-2H-1, 3, 5-thiadiazine-2-thione derivatives
Dolores Molero, Rolando P¨¦rez, Roberto Martinez, Margarita Su¨¢rez, Hortensia Rodriguez, Nazario Mart¨ªn and Carlos Seoane
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     compound 1
C14H21N2OPS     ÏàËÆ¶È:53.8%
Tetrahedron Letters          2004          45          3855-3859
Synthesis of chiral ortho-thio-substituted phenyl phosphonodiamidates via a P-S to P-C rearrangement
Christelle Mauger, Michel Vazeux, Serge Masson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     compound 7
    ÏàËÆ¶È:53.8%
Tetrahedron Letters          1991          32          7001-7004
Structure and synthesis of a new butanolide from a marine actinomycete
Charles Pathirana, Ryan Dwight, Paul R. Jensen, William Fenical, Antonio Delgado, Linda S. Brinen, Jon Clardy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     (Z)-3,7-dimethyl-6,7-isopropylidenedioxy-2-octenal
C13H22O3     ÏàËÆ¶È:53.8%
Russian Journal of Organic Chemistry          2002          38          1594-1605
Transformations of 6,7-Epoxy Derivatives of Citral and Citronellal in Various Acidic Media
O. I. Yarovaya, O. V. Salomatina, D. V. Korchagina, M. P. Polovinka and V. A. Barkhash
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     (3-methyl-3-butenyl)dicyclohexylphosphane sulfide
C17H31PS     ÏàËÆ¶È:53.8%
European Journal of Organic Chemistry          2010                   1562-1568
nBuLi-Mediated Hydrophosphination: A Simple Route to Valuable Organophosphorus Compounds
Arnaud Perrier, Virginie Comte, Claude Moïse, Philippe Richard and Pierre Le Gendre
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     (2-phenylethyl)dicyclohexylphosphane sulfide
    ÏàËÆ¶È:53.8%
European Journal of Organic Chemistry          2010                   1562-1568
nBuLi-Mediated Hydrophosphination: A Simple Route to Valuable Organophosphorus Compounds
Arnaud Perrier, Virginie Comte, Claude Moïse, Philippe Richard and Pierre Le Gendre
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     (4S)-7-bromo-p-methyl-1-en-8-ol
    ÏàËÆ¶È:53.8%
Australian Journal of Chemistry          1992          45          2077-2081
¦Ä-Terpineol
SD Bull and RM Carman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     racemic p-menth-1-ene-7,8-diol
C10H18O2     ÏàËÆ¶È:53.8%
Australian Journal of Chemistry          1993          46          441-447
7-Hydroxy- l,8-cineole and 7-Cineolic Acid. Two New Possum Urinary Metabolites
SD Bull, RM Carman, FN Carrick and KD Klika
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     compound 11b
C16H32O2Si     ÏàËÆ¶È:53.8%
Australian Journal of Chemistry          1996          49          741-749
7,9-Dihydroxy-1,8-cineole and 2¦Á,7-Dihydroxy-1,8-cineole: Two New Possum Urinary Metabolites
RM Carman and AC Garner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     ¦Á-(1R,2R,4S)-1,2-epoxy-p-mentha-7,8-diol
C16H32O3Si     ÏàËÆ¶È:53.8%
Australian Journal of Chemistry          1996          49          741-749
7,9-Dihydroxy-1,8-cineole and 2¦Á,7-Dihydroxy-1,8-cineole: Two New Possum Urinary Metabolites
RM Carman and AC Garner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     8-hydroxy-p-menth-1-en-7-al
C10H16O2     ÏàËÆ¶È:53.8%
Australian Journal of Chemistry          1996          49          741-749
7,9-Dihydroxy-1,8-cineole and 2¦Á,7-Dihydroxy-1,8-cineole: Two New Possum Urinary Metabolites
RM Carman and AC Garner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     (+)-¦Á-terpineol
    ÏàËÆ¶È:53.8%
Indian Journal of Chemistry Section B          1999          38B          515-517
Microbial oxidation of ¦Á-pinene to(+)-¦Á-terpineol by Candida tropicalis
T Chatterjee, B K De & D K Bhattacharyya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     oleuropeic acid
    ÏàËÆ¶È:53.8%
Journal of Guangdong Phamaceutical University          2008          24          33-35
Chemical constituents of the extracts from Ledum palustre L.Var. Angustum E.Busch(¢ò)
HUANG Ying, ZHANG De-zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     terpineol
    ÏàËÆ¶È:53.8%
Chinese Journal of Natural Medicines          2013          11          264-268
Chemical constituents of Cinnamomum cebuense
Consolacion Y. Ragasa, Dinah L. Espineli, Esperanza Maribel G. Agoo, Ramon S. del Fierro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     2-azacycloundecanone
C10H19NO     ÏàËÆ¶È:53.8%
The Journal of Organic Chemistry          2002          67          245-258
Motuporamines, Anti-Invasion and Anti-Angiogenic Alkaloids from the Marine Sponge Xestospongia exigua (Kirkpatrick): Isolation, Structure Elucidation, Analogue Synthesis, and Conformational Analysis
David E. Williams, Kyle S. Craig, Brian Patrick, Lianne M. McHardy, Rob van Soest, Michel Roberge, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     (E,Z)-oxacyclotetradec-11-en-2-one
    ÏàËÆ¶È:53.8%
Tetrahedron          2013          69          7408-7415
Efficient, durable and reusable olefin metathesis catalysts with high affinity to silica gel Original Research Article
Krzysztof Skowerski, Piotr Kasprzycki, Michał Bieniek, Tomasz K. Olszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     ¦Á-terpineol
    ÏàËÆ¶È:53.8%
Molecules          2013          18          10733-10746
Identification of Repellent and Insecticidal Constituents of the Essential Oil of Artemisia rupestris L. Aerial Parts against Liposcelis bostrychophila Badonnel
Xin Chao Liu, Yin Ping Li, He Qin Li, Zhi Wei Deng, Ligang Zhou, Zhi Long Liu and Shu Shan Du
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     compound 49
    ÏàËÆ¶È:53.8%
Organic Magnetic Resonance          1975          7          426-432
13C-NMR-Spektren von Monoterpenen
F. Bohlmann, R. Zeisberg and E. Klein
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     1-Cyclohexylidene-3-fluoro-2-oxaspiro[4.5]dec-3-ene
C15H21FO     ÏàËÆ¶È:53.8%
Synthesis          2014          46          1493-1505
Nucleophilic 5-endo-trig Cyclization of 3,3-Difluoroallylic Metal Enolates and Enamides:Facile Synthesis of Ring-Fluorinated Dihydroheteroles
Fujita, Takeshi; Ikeda, Masahiro; Hattori, Masahiro; Sakoda, Kotaro; Ichikawa, Junji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     cis-1-amino-octahydro-quinolizin-4-one
C9H16N2O     ÏàËÆ¶È:53.8%
Tetrahedron          2012          68          5547-5553
Reductive transformations of unsaturated azabicyclic nitrolactams
Mih¨¢ly Viktor Pilipecz, Tam¨¢s R¨®bert Varga, P¨¢l Scheiber, Zolt¨¢n Mucsi, Am¨¦lie F¨¤vre-Mourgues, S¨¢ndor Boros, L¨¢szl¨® Bal¨¢zs, G¨¢bor T¨®th, P¨¦ter Nemes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     p-Menth-1-en-8-ol
    ÏàËÆ¶È:53.8%
Journal of Agricultural and Food Chemistry          2006          54          9079-9084
Odor-Active Alcohols from the Fungal Transformation of ¦Á-Farnesene
Ulrich Krings, Björn Hardebusch, Dieter Albert, Ralf G. Berger, Mario Mar¨®stica, Jr., and Glaucia M. Pastore
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     1-(1-methyl-1-isothiocyano-ethyl)-4-methyl-3-cyclohexene
C11H16O     ÏàËÆ¶È:53.8%
Journal of the Brazilian Chemical Society          2001          12          661-666
Controlling Factors Determining the Selective HSCN Addition to Double Bonds and Their Application to the Synthesis of 7-Isothiocyano-7,8-¦Á-Dihydro-Bisabolene
Cec¨ªlia M. de Oliveira, Cleuza C. da Silva, Carol H. Collins and Anita J. Marsaioli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     2-(4-Methylcyclohex-3-enyl)propan-2-ol
    ÏàËÆ¶È:53.8%
Tetrahedron          2012          68          7414-7421
Amberlyst®-15: a reusable heterogeneous catalyst for the dehydration of tertiary alcohols
Lu¨ªs M.T. Frija, Carlos A.M. Afonso
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     9-Methyl-(Z)-5-decenyl Acetate
C13H24O2     ÏàËÆ¶È:53.8%
Journal of Chemical Ecology          1991          17          103-122
Alkyl substitution in terminal chain of (Z)-5-decenyl acetate, a pheromone component of turnip moth,Agrotis segetum. Synthesis, single-sensillum recordings, and structure-activity relationships
Stig Jönsson, Tommy Liljefors, Bill S. Hansson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     11-Oxa-(Z)-5-dodecenyl Acetate
C13H24O3     ÏàËÆ¶È:53.8%
Journal of Chemical Ecology          1995          21          815-832
Alkyl ether and enol ether analogs of (Z)-5-decenyl acetate, a pheromone component of the turnip moth,Agrotis segetum: probing a proposed bioactive conformation for chain-elongated analogs
Anna-Lena Gustavsson, Tommy Liljefors, Bill S. Hansson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     terpineol
C10H18O     ÏàËÆ¶È:53.8%
Chemistry and Industry of Forest Products          2014          34          71-76
Chemical Constituents of Ginkgo Biloba L.Leaves Lipids
TAO Ranl, WANG Cheng-zhang.KONG Zhen-wul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     6,6'-((6-(but-3-yn-1-ylamino)-1,3,5-triazine-2,4-diyl)bis(azanediyl))dihexanoic acid
C19H30N6O4     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry          2014          22          6288-6296
Sequential and parallel dual labeling of nanoparticles using click chemistry
Hong Zong, Sascha N. Goonewardena, Huai-Ning Chang, James B. Otis, James R. Baker Jr.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     (1S,2R,5S,6R,7R)-N,2-Dimethyl-5-(1-methylethyl)bicyclo[4.1.0]heptane-7-carboxamide
C13H23NO     ÏàËÆ¶È:53.8%
Chemistry & Biodiversity          2014          11          1782-1797
Synthesis and Sensory Studies of Umami-Active Scaffolds
Michael Backes, Susanne Paetz, Tobias Vössing and Jakob Peter Ley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     compound 5a
C16H30O5S     ÏàËÆ¶È:53.3%
Chinese Chemical Letters          2008          19          403-405
Synthesis of macrocyclic lactones with methoxysulfonyl side chain
Chuan Jin Hou, Xiao Mei Liang, Jing Ping Wu, Dao Quan Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     compound 1
C15H22O2     ÏàËÆ¶È:53.3%
Phytochemistry          1998          47          301-302
A sesquiterpene class from Illicium dunnianum
Lai-King Sy, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     lippifolian-1(6)-en-4¦Â-ol-5-one
CI5H22O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1994          Vol 57          206
Minor Constituents of Lippia integrifolia
Cesar A. N. Catal¨¢n, Marina E. P. de Lampasona, In¨¦s J. S. de Fenik, Carlos M. Cerda-Garc¨ªa-Rojas, Yolanda Mora-P¨¦rez, Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     eleganthol
C15H26O3     ÏàËÆ¶È:53.3%
Phytochemistry          1993          32          1493-1497
Eleganthol, a sesquiterpene from Clitocybe elegans
Alberto Arnone, Arturo Colombo, Gianluca Nasini, Stefano Valdo Meille
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     Methyl (1Z)-Cyclotridec-1-ene-1-carboxylate
    ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2012          95          428-447
Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone
Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     rac-(6Z)-1-Oxaspiro[2.14]heptadec-6-ene
    ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2012          95          428-447
Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone
Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     (6E)-1,4-Dioxaspiro[4.15]icos-6-ene
    ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2012          95          428-447
Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone
Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     Cyclohexan-carbaldehyde
    ÏàËÆ¶È:53.3%
Tetrahedron Letters          2001          42          6531-6534
Isochromans from 2-(3',4'-dihydroxy)phenylethanol
Marcella Guiso, Carolina Marra, Claudia Cavarischia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     compound 2
    ÏàËÆ¶È:53.3%
Tetrahedron          1986          42          2707-2716
13C NMR and 1H lanthanide induced shifts of naturally occurring alkamides with cyclic amide moieties -amides from achilleafalcata
Otmar Hofer, Harald Greger, Wolfgang Robien, Andreas Werner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     compound 21
C23H49N3     ÏàËÆ¶È:53.3%
The Journal of Organic Chemistry          2002          67          245-258
Motuporamines, Anti-Invasion and Anti-Angiogenic Alkaloids from the Marine Sponge Xestospongia exigua (Kirkpatrick): Isolation, Structure Elucidation, Analogue Synthesis, and Conformational Analysis
David E. Williams, Kyle S. Craig, Brian Patrick, Lianne M. McHardy, Rob van Soest, Michel Roberge, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
63 .     compound 9(n=10)ketone
    ÏàËÆ¶È:53.3%
Canadian Journal of Chemistry          1977          55          3261-3267
13C chemical shifts in medium ring and macrocyclic ketolactones
Jaswant R. Mahajan, Hugo C. Ara¨²jo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
64 .     compound 9(n=10)oxime
    ÏàËÆ¶È:53.3%
Canadian Journal of Chemistry          1977          55          3261-3267
13C chemical shifts in medium ring and macrocyclic ketolactones
Jaswant R. Mahajan, Hugo C. Ara¨²jo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
65 .     (Z)-3-(Cyclododec-1-en-1-yl)propanal
    ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2011          94          1216-1225
A Novel Synthesis of ¦Ã,¦Ä-Unsaturated Aldehydes from ¦Á-Formyl-¦Ã-lactones
Roger L. Snowden*, Robert Brauchli, and Simon Linder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
66 .     rel-(2R,8S,8aR)-2-(1,2,6,7,8,8a-Hexahydro-8,8a-dimethyl-2-naphthyl)-propan-2-ol
    ÏàËÆ¶È:53.3%
Flavour and Fragrance Journal          1995          10          147-152
Agarwood oil (Aquilaria agallocha Roxb.) Its composition and eight new valencane-,eremophilane- and vetispirane- derivatives
R. Näf, A. Velluz, R. Brauchli and W. Thommen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
67 .     Trichodone A
C15H26O3     ÏàËÆ¶È:53.3%
Chemistry & Biodiversity          2012          9          1205-1212
Sesquiterpenes and Cyclopeptides from the Endophytic Fungus Trichoderma asperellumSamuels, Lieckf. & Nirenberg
Gang Ding, Amanda Juan Chen, Jin Lan, Hongwu Zhang, Xiangdong Chen, Xingzhong Liu and Zhongmei Zou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
68 .     (4¦Á,7¦Â,9¦Á)-Farfugane-4,9,11-triol
C15H28O3     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2013          96          445-451
Six Novel Eudesmane-Like Sesquiterpenes from Illicium spathulatum
Xu-Jun Dong and Shi-De Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
69 .     cyclonerodiol
C15H28O3     ÏàËÆ¶È:53.3%
Journal of Shenyang Pharmaceutical University          2013          30          342-345
Secondary metabolites from marine sponge-associated fungus Hansfordia sp.
ZHAO Dan-qi, WU Ze-hong, LIU Dong, PEI Yue-hu, LIN Wen-han, BAI Jiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
70 .     isotripiperideine
    ÏàËÆ¶È:53.3%
Zeitschrift f¨¹r Naturforschung C          1988          43          363-369
On the Role of ¡÷1-Piperideine and Tripiperideine in the Biosynthesis of Quinolizidine Alkaloids
Ralf Perrey and Michael Wink
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
71 .     rac-1-Oxaspiro[2.15]octadec-7-ene
    ÏàËÆ¶È:52.9%
Helvetica Chimica Acta          2012          95          428-447
Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone
Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
72 .     N-[(2E,4E,8Z,)-tetradecatrienoyl]piperidine
C19H31NO     ÏàËÆ¶È:52.9%
Journal of Agricultural and Food Chemistry          2005          53          1435-1439
Piperidinyl Amides with Insecticidal Activity from the Maritime Plant Otanthus maritimus
Lito Christodoulopoulou, Maria Tsoukatou, Leto A. Tziveleka, Constantinos Vagias, Panos V. Petrakis, and Vassilios Roussis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
73 .     eiseniaiodide B
C18H29IO3     ÏàËÆ¶È:50%
Journal of Natural Products          2003          66          1318-1323
Novel Oxylipin Metabolites from the Brown Alga Eisenia bicyclis
Kenji Kousaka, Nobuyuki Ogi, Yasutomo Akazawa,Makiko Fujieda, Yuzo Yamamoto, Yuuki Takada, and Junji Kimura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
74 .     cyclonerodiol oxide
C15H29O3     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1984          32          4419-4425
Fungal Metabolites. II. Structural Elucidation of Minor Metabolites, Valinotricin, Cyclonerodiol Oxide, and Epicyclonerodiol Oxide, from Trichoderma polysporum
TETSURO FUJITA,YOSHIHISA TAKAISHI,YOSHIO TAKEDA,TETSUJI FUJIYAMA and TAKAHITO NISHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
75 .     3-[(2H3)Methyl]cyclopentadecanone
    ÏàËÆ¶È:50%
Helvetica Chimica Acta          2009          92          1782-1799
Synthesis of Deuterium-Labeled Perfume Ingredients as Internal Standards for Their GC/MS Quantification
Christian Chapuis, Carole Cantatore, Peter Fankhauser, Ren¨¦ Challand, Jean-Jacques Riedhauser
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
76 .     5,16-Dioxo-1-azacyclohexadecane-2-carbonitrile
C16H26N2O2     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2009          92          2774-2782
Synthesis of 15-Cyano-12-oxopentadecano-15-lactone and 15-Cyano- 12-oxopentadecano-15-lactam
Peng Wu, Xiao-Mei Liang, Jian-Jun Zhang, Yue-Mei Jia, Yan-Hong Dong, Jia-Xing Huang, Fu-Heng Chen, Dao-Quan Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
77 .     compound 2
C14H24O4     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry Letters          2011          21          2456-2459
Biotransformation of natural compounds. Oxido-reduction of Sch-642305 by Aspergillus ochraceus ATCC 1009
Emilie Adelin, Claudine Servy, Sylvie Cortial, H¨¦l¨¨ne L¨¦vaique, Jean François Gallard,Marie-Th¨¦r¨¨se Martin, Pascal Retailleau, Boonsom Bussaban, Saisamorn Lumyong, Jamal Ouazzani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
78 .     (4R,4aR,8aR)-4-isopropyl-6-methyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-ol
C14H24O     ÏàËÆ¶È:50%
The Journal of Organic Chemistry          2011          76          6558-6573
Total Synthesis of 10-Isocyano-4-cadinene and Its Stereoisomers and Evaluations of Antifouling Activities
Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata, Erina Yoshimura,Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
79 .     (4R,4aR,8aR)-4-isopropyl-6-methyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-ol
C14H24O     ÏàËÆ¶È:50%
The Journal of Organic Chemistry          2011          76          6558-6573
Total Synthesis of 10-Isocyano-4-cadinene and Its Stereoisomers and Evaluations of Antifouling Activities
Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata, Erina Yoshimura,Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
80 .     Hexyl-6-(2,5-dioxopyrrolidin-1-yl)hexanoate
C16H27NO4     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2012          20          86-95
Investigation of substituted 6-aminohexanoates as skin penetration enhancers
Katerina Brychtova, Lenka Dvorakova, Radka Opatrilova, Ivan Raich, Sandra Kacerova,Lukas Placek, Danuta S. Kalinowski, Des R. Richardson, Josef Jampilek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
81 .     Methyl (1Z)-Cyclododec-1-ene-1-carboxylate
    ÏàËÆ¶È:50%
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