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tomorrowwillbebetter
2Â¥2014-10-31 17:13:12
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lanseyimi

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2Â¥: Originally posted by lilithanks at 2014-10-31 17:13:12
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3Â¥2014-10-31 17:32:17
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lilithanks

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3Â¥: Originally posted by lanseyimi at 2014-10-31 17:32:17
ÄÜ·ñ°ïÎÒ¸´ÖÆÒ»Ï£¬²»ÒªÓÃͼƬ¸ñʽ£¿ÕâÑùÎÒ²éÎÄÏײ»ºÃŪ£¬Ð»Ð»ÁË...

1 .     ent-trichoacorenol
C17H30O     ÏàËÆ¶È:80%
European Journal of Organic Chemistry          2011                   5167-5175
Enantioselective Synthesis of the Unnatural Enantiomers of the Fungal Sesquiterpenoids Acorenone and Trichoacorenol
Nelson L. Brock and Jeroen S. Dickschat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (4E,8R)-caryophyll-4(5)-ene-8,12-diol
C15H24O     ÏàËÆ¶È:73.3%
Journal of Natural Products          2000          63          44-47
Biotransformation of (4E,8R)-Caryophyll-4(5)-en-8-ol by Botrytis cinerea
Rosa Dur¨¢n-Patr¨®n, Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     1S*,4S*,5S*, Acora-8(15),9-dien-7R*-ol(3a)
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          2005          53(5)          515-518
Chemical Constituents of Malagasy Liverworts, Part III:Sesquiterpenoids from Bazzania decrescens and Bazzania madagassa
Liva HARINANTENAINA, Ritsu KURATA, and Yoshinori ASAKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3,7-dimethyl-3-(1'E)-pentenyl-7-hydroxy-5-(E)-okten-1-ol
    ÏàËÆ¶È:66.6%
Phytochemistry          1992          31          2355-2357
Uncommon type of hydroxylation of 3-alkenylsubstituted derivatives of citronellol and citronellic acid by Spirodela punctata
Paweł Pawłowicz, Czesław Wawrze¨½czyk, Antoni Siewi¨½ski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (3R,5S,8S)-5-heptyl-3-methylpyrrolizidine
C15H29N     ÏàËÆ¶È:66.6%
Heterocycles          2009          79          1043-1060
Catalytic Asymmetric Synthesis of Both Enantiomers of Pyrrolizidines 223H', 239K', 265H', and 267H' Found in Madagascan Frogs (Mantella) and Their Affinities for Nicotinic Acetylcholine Receptor
Yukako Saito, Seiki Takahashi, Nehad Azer, Amira T. Eldefrawi, Mohyee E. Eldefrawi, and Hiroki Takahata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Compound 4b
C27H49NO     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry Letters          2009          19          5764-5768
Simple dihydrosphyngosine analogues with potent activity against MDR-Mycobacterium tuberculosis
Esther del Olmo, Gloria Mar¨ªa Molina-Salinas, Ricardo Escarcena, Mario Alves, Jos¨¦ L. L¨®pez-P¨¦rez, Rogelio Hernandez-Pando, Salvador Said-Fern¨¢ndez, Arturo San Feliciano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     shizuka-acoradienol
C15H24O     ÏàËÆ¶È:66.6%
Chinese Journal of Natural Medicines          2008          6          404-407
A New Sesquiterpenoid from the Roots of Chloranthus fortunei
WANG Xia-Chang; WU Wei-Qun; MA Shi-Ping; LIU Jing-Han; HU Li-Hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3-(Tetrahydrofuran-2-yl)-decane-1,3-diol
C14H28O3     ÏàËÆ¶È:66.6%
Tetrahedron Letters          2002          43          8007-8010
Catalytic Barbier-type reactions of lactones and esters mediated by the Mischmetall/SmI2(cat.) system or the Mischmetall/[SmI2/NiI2(cat'.)](cat.) system
Marie-Isabelle Lannou, Florence H¨¦lion, Jean-Louis Namy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     shizuka-acoradienol
C15H24O     ÏàËÆ¶È:66.6%
Agricultural and Biological Chemistry          1984          48          713-717
Structures of Novel Sesquiterpene Alcohols from Chloranthus japonicus (Chloranthaceae)
Jim KAWABATA, Yukiharu FUKUSHI, Satoshi TAHARA, Junya MIZUTANI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Isodauc-6-ene-10¦Â,14-diol
C15H26O2     ÏàËÆ¶È:66.6%
Journal of Asian Natural Products Research          2012          14          224-234
Sesquiterpenes from Dysoxylum oliganthum and Dysoxylum excelsum
Hong-Bing Liu, Chuan-Rui Zhang, Shi-Hui Dong, Sheng-Ping Yang, Qi Sun, Mei-Yu Geng & Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     N-Octanoylpyrrolidine
C12H23NO     ÏàËÆ¶È:66.6%
Journal of Agricultural and Food Chemistry          1999          47          3866-3871
Synthesis and Biological Evaluation of New Analogues of the Active Fungal Metabolites N-(2-Methyl-3-oxodecanoyl)-2-pyrroline and N-(2-Methyl-3-oxodec-8-enoyl)-2-pyrroline
Pilar Moya, ¨¢ngel Cant¨ªn, Miguel A. Miranda, Jaime Primo, and Eduardo Primo-Y¨²fera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (2S,3R,4S)-Penazetidine A
C23H47O2N     ÏàËÆ¶È:66.6%
European Journal of Organic Chemistry          1996          1996          1083-1089
Synthesis of Sphingosine Relatives, XVIII!. Synthesis of Penazetidine A, an Alkaloid Inhibitor of Protein Kinase C Isolated from the Marine Sponge Penares sollasi
Arata Yajima, Hirosato Takikawa and Kenji Mori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     trichoacorenol
    ÏàËÆ¶È:66.6%
Journal of Chinese Pharmaceutical Sciences          2014          23          421-424
Two terpenoids and a polyketide from the endophytic fungus Trichoderma sp. Xy24 isolated from mangrove plant Xylocarpus granatum
Min Zhang, Ning Li, Ridao Chen, Jianhua Zou, Chunmei Wang, Jungui Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
tomorrowwillbebetter
4Â¥2014-10-31 18:58:54
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