Compounds > 2-4-3--5--tetrahydroxystilbene

2-4-3--5--tetrahydroxystilbene and ethylene

2-4-3--5--tetrahydroxystilbene has been researched along with ethylene* in 1 studies

Other Studies

1 other study(ies) available for 2-4-3--5--tetrahydroxystilbene and ethylene

Article	Year
Syntheses of (-)-oleocanthal, a natural NSAID found in extra virgin olive oil, the (-)-deacetoxy-oleuropein aglycone, and related analogues. The Journal of organic chemistry, 2007, Aug-31, Volume: 72, Issue:18 Phenolic compounds extracted from extra virgin olive oil have attracted considerable recent attention. One of the components, (-)-oleocanthal (1), an inhibitor of the COX-1 and COX-2 enzymes, possesses similar potency as the NSAID ibuprofen. In this, a full account, we disclose the first- and now second-generation syntheses of both enantiomers of the oleocanthals, as well as the first synthesis of the closely related (-)-deacetoxy-oleuropein aglycone and a series of related analogues for structure activity studies. To demonstrate the utility of the second-generation synthesis, multigram quantities of (-)-oleocanthal were prepared in 10 steps (14% overall yield) from commercially available D-lyxose. Topics: Aldehydes; Anti-Inflammatory Agents, Non-Steroidal; Biological Products; Cerium; Chlorides; Cyclization; Cyclopentane Monoterpenes; Ethylenes; Iridoid Glucosides; Iridoids; Ketones; Molecular Structure; Olive Oil; Phenols; Plant Oils; Pyrans	2007

Article

Year

Syntheses of (-)-oleocanthal, a natural NSAID found in extra virgin olive oil, the (-)-deacetoxy-oleuropein aglycone, and related analogues.

The Journal of organic chemistry, 2007, Aug-31, Volume: 72, Issue:18

Phenolic compounds extracted from extra virgin olive oil have attracted considerable recent attention. One of the components, (-)-oleocanthal (1), an inhibitor of the COX-1 and COX-2 enzymes, possesses similar potency as the NSAID ibuprofen. In this, a full account, we disclose the first- and now second-generation syntheses of both enantiomers of the oleocanthals, as well as the first synthesis of the closely related (-)-deacetoxy-oleuropein aglycone and a series of related analogues for structure activity studies. To demonstrate the utility of the second-generation synthesis, multigram quantities of (-)-oleocanthal were prepared in 10 steps (14% overall yield) from commercially available D-lyxose.

Topics: Aldehydes; Anti-Inflammatory Agents, Non-Steroidal; Biological Products; Cerium; Chlorides; Cyclization; Cyclopentane Monoterpenes; Ethylenes; Iridoid Glucosides; Iridoids; Ketones; Molecular Structure; Olive Oil; Phenols; Plant Oils; Pyrans

2007