C-24 Stereochemistry of Marine Sterols: (22E)-24-(Isopropenyl)-22-dehydrocholesterol and 24-Isopropenylcholesterol
Author:
Affiliation:
1. Department of Chemistry and Materials Science, Tokyo Institute of Technology
2. Departamento de Química, Universidad Nacional de Colombia
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb/54/10/54_10_1473/_pdf
Reference16 articles.
1. Ophirasterol, a new C31 sterol from the marine sponge Topsentia ophiraphidites
2. 2) Echigo S., Calderon G. J., Castellanos L., Duque C., Hara N., Fujimoto Y., Steroids, 72 (2007), in press.
3. Stereospecific synthesis of the side chain of the steroidal plant sex hormone oogoniol
4. Stereochemie einer Claisen‐Umlagerung in der Sterin‐Seitenkette
5. [3,3]-Claisen rearrangements in 24α-methyl steroid synthesis
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1. C-24 Stereochemistry of Marine Sterols: (22E)-25,28-Dimethyl-stigmasta-5,22,28-trien-3β-ol and 25,28-Dimethylstigmasta-5,28-dien-3β-ol;Natural Product Communications;2014-12
2. Porifera (Sponges)-5;Encyclopedia of Marine Natural Products;2014-08-07
3. Porifera (Sponges)-2;Encyclopedia of Marine Natural Products;2014-08-07
4. C-24 stereochemistry of marine Sterols: (22E)-24-Ethyl-24-methylcholesta-5,22-dien-3b-oβl and 24-Ethyl-24-methylcholest-5-en-3β-ol;Journal of the Brazilian Chemical Society;2011-05
5. Antifouling Activities against Colonizer Marine Bacteria of Extracts from Marine Invertebrates Collected in the Colombian Caribbean Sea and on the Brazilian Coast (Santa Catarina);Zeitschrift für Naturforschung C;2011
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