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1 .     10-Eicosanol
C20H42O     ÏàËÆ¶È:88.8%
Phytochemistry Letters          2008          1          89-93
Constituents of Nelumbo nucifera leaves and their antimalarial and antifungal activity
Vijai K. Agnihotri, Hala N. ElSohly, Shabana I. Khan, Melissa R. Jacob, Vaishali C. Joshi, Troy Smillie, Ikhlas A. Khan, Larry A. Walker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 1
C30H62O     ÏàËÆ¶È:88.8%
Phytochemistry          1998          49          755-756
A long chain alcohol from Argemone mexicana
Naresh K. Sangwan, Mangel S. Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     nonacosan-10-ol
    ÏàËÆ¶È:88.8%
Phytochemistry          1987          26          793-794
Hirsudiol a triterpenoid from cocculus hirsutus
Viqar Uddin Ahmad,Faryal Vali Mohammad,Tahir Rasheed
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 4a
    ÏàËÆ¶È:88.8%
Chinese Journal of Chemistry          2009          27          2217-2222
Reactivity-based One-pot Synthesis of Immunosuppressive Glycolipids from the Caribbean Sponge Plakortis simplex
Guokai L¨¹, Peng Wang, Qingchao Liu, Zaihong Zhang, Wei Zhang and Yingxia Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 4b
    ÏàËÆ¶È:88.8%
Chinese Journal of Chemistry          2009          27          2217-2222
Reactivity-based One-pot Synthesis of Immunosuppressive Glycolipids from the Caribbean Sponge Plakortis simplex
Guokai L¨¹, Peng Wang, Qingchao Liu, Zaihong Zhang, Wei Zhang and Yingxia Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 4c
    ÏàËÆ¶È:88.8%
Chinese Journal of Chemistry          2009          27          2217-2222
Reactivity-based One-pot Synthesis of Immunosuppressive Glycolipids from the Caribbean Sponge Plakortis simplex
Guokai L¨¹, Peng Wang, Qingchao Liu, Zaihong Zhang, Wei Zhang and Yingxia Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (8S,11S,E)-octadec-9-ene-8,11-diol
C18H36O2     ÏàËÆ¶È:88.8%
The Journal of Organic Chemistry          2010          75          4230-4243
Asymmetric Synthesis of the Cytotoxic Marine Natural Product (t)-Awajanomycin and Its C-11 Epimer
Rui Fu, Jian-Liang Ye, Xi-Jie Dai, Yuan-Ping Ruan, and Pei-Qiang Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     ginnol
    ÏàËÆ¶È:88.8%
Chinese Joumal of Experimental Traditional Medical Fomulae          2012          18          122-125
Studies on Chemical Constituents of Effective Fraction of Honeysuckle on Inhibition of Escherichia coli Biofilms
XU Duo-duo, JIANG Xiang-zhi, GAO Yang, ZHENG Wei, HE Min, GAO Qi-pin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     19-hexatetracontanol
    ÏàËÆ¶È:80%
Natural Product Research          2010          24          34-39
A new analogue of fatty alcohol from Tamarix hampeana L.
Ahmet Aykaç; Yurdanur Akg¨¹l
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (S)-Dec-1-yn-3-ol
    ÏàËÆ¶È:80%
Tetrahedron          2012          68          8431-8440
Tellurium in organic synthesis: a general approach to buteno- and butanolides
Renan S. Ferrarini, Alcindo A. Dos Santos, João V. Comasseto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (S)-Dec-1-yn-3-ol
    ÏàËÆ¶È:80%
Tetrahedron          2012          68          10601-10610
Tellurium in organic synthesis: a general approach to buteno- and butanolides
Renan S. Ferrarini, Alcindo A. Dos Santos, João V. Comasseto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ¶þÊ®¾ÅÍé-15-´¼
C29H60O     ÏàËÆ¶È:80%
Journal of Chinese Medicinal Materials          2006          29          565-567
Ѫˮ²ÝµØÉϲ¿·ÖÇ×Ö¬ÐԳɷÖÑо¿
¶Å·½Â´, ÕÅÑÞ, Ö£¹ú¶°, Å·ÑôÎÄ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     tetracosane-1,3-diol
    ÏàËÆ¶È:80%
Chinese Joumal of Experimental Traditional Medical Fomulae          2011          17          92-94
Chemical Constituents of Polygonum capitatum ¢ò
YANG Yang, YANG Ying-bo, ZHU Bin, WU Zhi-jun, CHEN Wan-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     4-Nonanol
C9H20O     ÏàËÆ¶È:77.7%
Phytochemistry          2004          65          2163-2166
Volatile constituents of Capillipedium parviflorum
Umar Mahmood, Vijay K. Kaul, Ruchi Acharya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     10-nonacosanol
C29H60O     ÏàËÆ¶È:77.7%
Journal of Chinese Pharmaceutical Sciences          2000          9          6-9
Chemical constituets of Chaenomeles sinensis
Sun Lianna and Hong Yongfu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Compound 26
C7H18O6P2     ÏàËÆ¶È:77.7%
Bioorganic & Medicinal Chemistry Letters          2003          13          3231-3235
Bisphosphonates derived from fatty acids are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase
Sergio H. Szajnman, Andrea Montalvetti, Youhong Wang, Roberto Docampo, Juan B. Rodriguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (R)-Docosan-3-ol
C22H46O     ÏàËÆ¶È:77.7%
Journal of the Chemical Society, Perkin Transactions 1          1999                   513-518
Chemoenzymatic synthesis of (+)-docosa-4,15-dien-1-yn-3-ol, a component of the marine sponge Cribrochalina vasculum, and confirmation of the structure and absolute configuration of the acetylenic alcohol, by lipase-catalysed biotransformations
Kiyoshi Morishita, Makoto Kamezawa, Takehiko Ohtani, Hojun Tachibana, Mayumi Kawase, Midori Kishimoto and Yoshinobu Naoshima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     1-Iodo-2-octanol
    ÏàËÆ¶È:77.7%
Molecules          2012          17          5508-5519
H2TPP Organocatalysis in Mild and Highly Regioselective Ring Opening of Epoxides to Halo Alcohols by Means of Halogen Elements
Parviz Torabi, Javad Azizian and Shahab Zomorodbakhsh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     (¡À)- and meso-heptadecane-7,11-diol
    ÏàËÆ¶È:77.7%
European Journal of Organic Chemistry          2004          2004          1198-1201
Synthesis and Enantioselective Gas Chromatography of Stereoisomers of 7,11-Dimethylheptadecane − A Pheromone Component of Lambdina Species
Sharon Chow, Wilfried A. Koenig and William Kitching
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (7S,11S)-heptadecane-7,11-diol
    ÏàËÆ¶È:77.7%
European Journal of Organic Chemistry          2004          2004          1198-1201
Synthesis and Enantioselective Gas Chromatography of Stereoisomers of 7,11-Dimethylheptadecane − A Pheromone Component of Lambdina Species
Sharon Chow, Wilfried A. Koenig and William Kitching
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (3S)-non-1-yn-3-ol
    ÏàËÆ¶È:77.7%
Chemistry-A European Journal          2005          11          639-649
An Asymmetric Formal Synthesis of Fasicularin
Michaël D. B. Fenster and Gregory R. Dake
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     dioctyl ether
    ÏàËÆ¶È:77.7%
Magnetic Resonance in Chemistry          1991          29          273-281
Carbon-13 NMR relaxation study of the overall and internal motions in compounds containing n-octyl chains
Lucy M. Bull, Duncan G. Gillies, Stephen J. Matthews, Leslie H. Sutcliffe and Antony J. Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     octacosane-10-ol-21-ene
    ÏàËÆ¶È:77.7%
Indian Journal of Chemistry Section B          2002          41B          1088-1092
Novel diterpenoid and aliphatic compounds from Thuja orientalis
B K Mehta, Vibha Nagar, Satish Shitut, Sanjay Nagar, Sanjay Sharma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Sodium [3-13C]Octanoate
    ÏàËÆ¶È:77.7%
Journal of the American Chemical Society          1988          110          2938-2945
Biosynthesis and full NMR assignment of fungichromin, a polyene antibiotic from Streptomyces cellulose
Hiroshi. Noguchi, Paul H. Harrison, Kunizo. Arai, Thomas T. Nakashima, Laird A. Trimble, John C. Vederas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     10-ôÇ»ù-¶þÊ®Íé
    ÏàËÆ¶È:77.7%
Journal of Anhui Agricultural Sciences          2008          36          7229-7230
Study on Chemical Constituents of Juniperus formosana
CHEN Hong-ying et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     öè¸Î´¼
    ÏàËÆ¶È:77.7%
Journal of Chinese Medicinal Materials          2001          24          266-268
À¶°ß±³¸Øº£Íû¯Ñ§³É·ÖÑо¿
ÁÖºñÎÄ, Æîº£ÁÖ, ÕÅ´¿, ÉòÑô, ¹ù³Î, ÉÛÔª¸£
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     Nonacosane-10-ol
C29H60O     ÏàËÆ¶È:77.7%
Journal of Agricultural and Food Chemistry          2013          61          5689-5695
Nematicidal Activity of Nonacosane-10-ol and 23a-Homostigmast-5-en-3¦Â-ol Isolated from the Roots of Fumaria parviflora (Fumariaceae)
Ishrat Naz, Saifullah, and M. R. Khan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     3S-nonanol
    ÏàËÆ¶È:77.7%
Chemistry of Natural Compounds          2005          41          643-649
Ozonolysis of Ricinolic Acid Derivatives and Transformations of the Ozonolysis Products under Barton Reaction Conditions
G. Yu. Ishmuratov, R. Ya. Kharisov, A. Kh. Shayakhmetova, L. P. Botsman, O. V. Shitikova, G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     Nonacosane-4,10-diol
C29H60O2     ÏàËÆ¶È:75%
Phytochemistry          1981          20          2711-2716
Epicuticular wax of Juniperus scopulorum
Alexander P. Tulloch, Lothar Bergter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     1-Bromo-6-methyldecane
    ÏàËÆ¶È:72.7%
Bioscience, Biotechnology, and Biochemistry          2010          74          119-124
Improved Synthesis of Three Methyl-Branched Pheromone Components Produced by the Female Lichen Moth
Tomonori TAGURI, Rei YAMAKAWA, Yasushi ADACHI, Kenji MORI and Tetsu ANDO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     compound 11
C19H40O2     ÏàËÆ¶È:72.7%
Tetrahedron          1997          53          16699-16710
Amphimic acids and related long-chain fatty acids as DNA topoisomerase I inhibitors from an Australian sponge, Amphimedon sp.: Isolation, structure, synthesis, and biological evaluation
Takayuki Nemoto, Go Yoshino, Makoto Ojika, Youji Sakagami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     compound 16
C19H39IO     ÏàËÆ¶È:72.7%
Tetrahedron          1997          53          16699-16710
Amphimic acids and related long-chain fatty acids as DNA topoisomerase I inhibitors from an Australian sponge, Amphimedon sp.: Isolation, structure, synthesis, and biological evaluation
Takayuki Nemoto, Go Yoshino, Makoto Ojika, Youji Sakagami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     (7R,10RS)-octadecane-7,10-diol
    ÏàËÆ¶È:72.7%
Russian Journal of Organic Chemistry          2008          44          1130-1133
Hydroboration-oxidation of ricinoleic acid derivatives
R. R. Muslukhov, A. Kh. Shayakhmetova, M. P. Yakovleva, O. V. Shitikova and G. Yu. Ishmuratov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     (2R,3R)-1,2,3-trihydroxydecane
    ÏàËÆ¶È:70%
Chemical & Pharmaceutical Bulletin          1990          38          1447-1450
Synthesis and Absolute Configurations of the Cytotoxic Polyacetylenes Isolated from the Callus of Panax ginseng
Yasuo FUJIMOTO,Mitsuru SATOH,Naoki TAKEUCHI and Makoto KIRISAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     2,5-di-[(8Z,11R)-11-hydroxy-heptadec-8-enyl]-1,3,4-oxadiazole
C36H66O2N2     ÏàËÆ¶È:70%
Chinese Chemical Letters          2008          19          2010-5-8
One-pot synthesis, antibacterial and antifungal activities of n o ve l 2 ,5 -disubstituted-1,3,4 oxadiazoles
Abdul Rauf£¬Shweta Sharma, Saloni Gangal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     2,5di-[(8R,11Z)-8-hydroxy-heptadec-11-enyl]-1,3,4-oxadiazole
C36H66O2N2     ÏàËÆ¶È:70%
Chinese Chemical Letters          2008          19          2010-5-8
One-pot synthesis, antibacterial and antifungal activities of n o ve l 2 ,5 -disubstituted-1,3,4 oxadiazoles
Abdul Rauf£¬Shweta Sharma, Saloni Gangal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     ¦Á-palmityl glycerin ether(ö޸δ¼)
C19H40O3     ÏàËÆ¶È:70%
Chinese Journal of Marine Drugs          2001          20(2)          12-15
Chemical study on secondary metabolites from ascidian Styela clava(I)
LAO Yan-bin, JIANG Ting, LI Jun, FU Hong-zheng, LIN Wen-han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     ö޸δ¼
    ÏàËÆ¶È:70%
Chinese Journal of Marine Drugs          2000          19(1)          1-3
STUDIES ON THE CHEMICAL CONSTITUENTS OF THE TUNICATE STYELACANOPUS FROM THE DAYAWAN BAY
Wang Chaojie, Su Jing yu, Zeng Longmei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     2-phenylselanyl-[1,2,3]-dithiaphosphinane-2-oxide
    ÏàËÆ¶È:70%
Tetrahedron Letters          2000          41          10195-10200
Generation of dialkyl phosphonodithioyl radicals and their addition onto alkenes. Synthesis of 3-phosphonodithiomethyl-3-deoxofuranosides
Chrystel Lopin, Arnaud Gautier, G¨¦raldine Gouhier, Serge R. Piettre
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     (¡À)-asarinol B
C10H14O3     ÏàËÆ¶È:70%
Phytochemistry          1990          29          3571-3574
Monoterpenes from asiasari radix from Asiasarum sp.
Kazunori Hashimoto,Takao Katsuhara,Hiroyuki Itoh,Yukinobu Ikeya,Minoru Okadaand,Hiroshi Mitsuhashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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