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1 .     (3R)-hydroxy-14-methyldocos-(4E)-en-1-yne
C23H42O     ÏàËÆ¶È:71.4%
Journal of Natural Products          1992          Vol 55          1275
Further Bioactive Acetylenic Compounds from the Caribbean Sponge Cribrochalina vasculum
Anna Aiello, Ernesto Fattorusso, Marialuisa Menna, Maurizio Pansini
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     (3R)-hydroxy-16-methyleicos-1-yne
C21H40O     ÏàËÆ¶È:71.4%
Journal of Natural Products          1992          Vol 55          1275
Further Bioactive Acetylenic Compounds from the Caribbean Sponge Cribrochalina vasculum
Anna Aiello, Ernesto Fattorusso, Marialuisa Menna, Maurizio Pansini
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     compound R-1(a)
    ÏàËÆ¶È:71.4%
Bioscience, Biotechnology, and Biochemistry          2001          65          2065-2069
Synthesis of Methyl (5Z,9Z,17R)-17-Methylnonadeca-5,9-dienoate, the (R)-Enantiomer of the Structure Proposed for a Metabolite of the Philippine Sponge Plakinastrella sp.
Miho TAKAGI, Hirosato TAKIKAWA, Kenji MORI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     (-)-(3S)-1-[(3S,6R,7S)-3-(tert-butyldimethylsilyloxy)-1-azaspiro[5.5]undec-7-yl]-nonan-3-ol
C25H51NO2Si     ÏàËÆ¶È:71.4%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     (R)-10,14-Dimethyl-1-pentadecanol
C17H34     ÏàËÆ¶È:71.4%
Journal of Chemical Ecology          1995          21          627-634
Absolute configuration of sex pheromone for tea tussock moth,Euproctis pseudoconspersa (strand)via synthesis of (R)- and (S)-10, 14-dimethyl-1-pentadecyl isobutyrates
Akio Ichikawa, Tetsuya Yasuda, Sadao Wakamura
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     3-Hydroxy-16-methyleicos-4(E)-en-1-yne
C21H38O     ÏàËÆ¶È:71.4%
The Journal of Organic Chemistry          1990          55          6223-6225
New acetylenic alcohols from the sponge Cribrochalina vasculum
Sarath P. Gunasekera, Glynn T. Faircloth
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     strongylodiol G
C24H42O2     ÏàËÆ¶È:70.8%
Journal of Natural Products          2005          68          1001-1005
Acetylenic Strongylodiols from a Petrosia (Strongylophora) Okinawan Marine Sponge
Kinzo Watanabe, Yuichiro Tsuda, Maki Hamada, Miki Omori, Go Mori,Kazuo Iguchi, Hideo Naoki, Tsuyoshi Fujita, and Rob W. M. Van Soest
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     Microginin 91-A oxazolizinone
C29H48N4O7     ÏàËÆ¶È:69.5%
Tetrahedron          2000          56          8643-8656
Microginins, Zinc Metalloproteases Inhibitors from the Cyanobacterium Microcystis aeruginosa
Keishi Ishida, Taku Kato, Masahiro Murakami, Masayuki Watanabe, Mariyo F. Watanabe
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     Cycloartenol
    ÏàËÆ¶È:68.1%
Phytochemistry          1984          23          2077-2079
Uvariastrol, a novel cycloartane triterpene from the stem bark of Uvariastrum zenkeri
Peter G. Waterman, Ilias Mohammad
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     Officinoic acid B
C22H38O4     ÏàËÆ¶È:68.1%
Journal of Natural Products          2011          74          1241-1247
Bioactive Terpenes from Spongia officinalis
Emiliano Manzo, M. Letizia Ciavatta, Guido Villani, Mario Varcamonti, S. M. Abu Sayem, Rob van Soest, and Margherita Gavagnin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     Methyl (2R,3R,23R)-3-acetoxy-2-docosyl-23-methyl-24-oxotetracosanoate
    ÏàËÆ¶È:68.1%
Tetrahedron          2014          70          7322-7335
Synthetic epoxy-mycolic acids
Dakhil Z. Al Kremawi, Juma'a R. Al Dulayymi, Mark S. Baird
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     melophlin S
C21H37NO     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          2006          54(6)          852-854
Melophlins P, Q, R, and S: Four New Tetramic Acid Derivatives, from Two Palauan Marine Sponges of the Genus Melophlus
Jinzhong XU,Masateru HASEGAWA,Ken-ichi HARADA,Hisayoshi KOBAYASHI, Hiroshi NAGAI,and Michio NAMIKOSHI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     compound 1
C41H83O4N     ÏàËÆ¶È:66.6%
Journal of Natural Products          2008          71(1)          513-515
Antiepileptic Ceramides from the Red Sea Sponge Negombata corticata
Safwat A. Ahmed, Sherief I. Khalifa, and Mark T. Hamann
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     (5Z,9Z)-17-methylnonadeca-5,9-dienoate
C21H38O2     ÏàËÆ¶È:66.6%
Journal of Natural Products          1998          61          1539-1542
New Cyclic Peroxides from the Philippine Sponge Plakinastrella sp.
Asfia Qureshi, Javier Salv¨¢ , Mary Kay Harper, and D. John Faulkner
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     methyl 11-methylpentadecanoate
C17H34O2     ÏàËÆ¶È:66.6%
Journal of Natural Products          1998          61          1049-1052
Identification and Total Synthesis of Novel Fatty Acids from the Caribbean Sponge Calyx podatypa
N¨¦stor M. Carballeira, Mayra Pag¨¢n, and Abimael D. Rodr¨ªguez
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     (5S)-hydroxy-16-methyleicos-(3Z)-en-1-yne
C21H38O     ÏàËÆ¶È:66.6%
Journal of Natural Products          1995          Vol 58          1801-1807
Antitumor Activity and Stereochemistry of Acetylenic Alcohols from the Sponge Cribrochalina vasculum
Yali F. Hallock, John H. Cardellina, Michael S. Balaschak, Mark R. Alexander, Tanya R. Prather, Robert H. Shoemaker, Micheal R. Boyd
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     Methyl 10-ketolactobacillate (Methyl (Z)-10-(2-hexylcyclopropane-1-yl)-10-oxodecanoate)
C20H36O3     ÏàËÆ¶È:66.6%
Organic Letters          2006          Vol. 8, No. 1          79-81
Configurational Analysis of Cyclopropyl Fatty Acids Isolated from Escherichia coli
Laura J. Stuart, James P. Buck, Amy E. Tremblay, and Peter H. Buist
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     Methyl 13-ketolactobacillate (Methyl (Z)-10-(2-(1-oxo)-hexylcyclopropane-1-yl)-decanoate)
C20H36O3     ÏàËÆ¶È:66.6%
Organic Letters          2006          Vol. 8, No. 1          79-81
Configurational Analysis of Cyclopropyl Fatty Acids Isolated from Escherichia coli
Laura J. Stuart, James P. Buck, Amy E. Tremblay, and Peter H. Buist
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     N,N,N-Trimethyl-3-(6-(2-dodecanoyloxazol-5-yl)hexylsulfonyl)-propan-1-ammonium iodide
C27H51N2O4S     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2012          20          1100-1112
Design, synthesis and evaluation of polar head group containing 2-keto-oxazole inhibitors of FAAH
Marion Rusch,Stefan Zahov,Ingrid R. Vetter, Matthias Lehr, Christian Hedberg
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     1-(tetrahydropyran-2-yloxy)-heptadecan-8-ol
    ÏàËÆ¶È:66.6%
Indian Journal of Chemistry Section B          2010          49B          1648-1652
Total synthesis of three natural products: Decyl 8-hydroxyheptadecanoate,undecyl hexadecanoate and 2,3-dihydroxypropyl hexadecanoate
Ashima Singh,M L Sharma & Jasvinder Singh*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



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