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of 96
pro vyhledávání: '"Couladouros, E.A."'
Autor:
Sagnou, M., Mitsopoulou, K.P., Koliopoulos, G., Pelecanou, M., Couladouros, E.A., Michaelakis, A.
Publikováno v:
In Acta Tropica September 2012 123(3):190-195
Akademický článek
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Akademický článek
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The oviposition pheromone of Culex quinquefasciatus was synthesized in a racemic form in a simple (five steps), efficient, high yielding (45% total yield), and low cost way (use of relatively low cost reagents). Our synthetic racemic pheromone (SRP)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::bf3d3e152889f5df6788ac726312f766
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3010735
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3010735
Platelet activating factor is one of the most potent inflammatory ether phospholipid mediators known and structurally modified analogues are of considerable interest as potential therapeutic preparations. Inspired by the proposed structure for a nove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::484a83f7a6afe59015ccb5fddcd80b41
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3067908
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3067908
Heterocyclic derivatives of naphthoquinones were synthesized via their 2-bromo-2,3-dehydro-intermediates. This new route may lead to the formation of benzo[a]phenothiazin-5-ones, benzo[f]quinoxalin-6-ones as well as their 1,4 (or 7,10) dihydroxy-deri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::ff86605c983986521fac8ef7f638d302
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3027487
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3027487
Autor:
Nicolaou, K.C., Theodorakis, E.A., Rutjes, F.P.J.T., Sato, M., Tiebes, J., Xiao, X.Y., Hwang, C.K., Duggan, M.E., Yang, Z., Couladouros, E.A., Sato, F., Shin, J., He, H.M., Bleckman, T.
Publikováno v:
Journal of the American Chemical Society, 117, 10239-10251. Amer chemical soc
Journal of the American Chemical Society, 117, 41, pp. 10239-10251
Journal of the American Chemical Society, 117, 41, pp. 10239-10251
Contains fulltext : 26295.PDF (Publisher’s version ) (Open Access)
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https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3803b1524f35d176515b68accb5bf70f
http://hdl.handle.net/2066/26295
http://hdl.handle.net/2066/26295
A simple and effective procedure for the resolution of 2, 3-dideoxy-DL-2-enopyranos-4- uloses is presented. This procedure is based on column chromatographic separation of their diastereomeric 0-(N-rm-butyloxycarbonyl)-L-alanyl esters, followed by mi
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https://explore.openaire.eu/search/publication?articleId=od______2127::18e331872d1240bcb657b6cae6439508
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3027659
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3027659
3-Deoxy-dl-prumycin (1) was synthesized from 2-furanmethanol (2-furfuryl alcohol, 2) in eleven steps in 15% total yield. Michael addition of azide anion to 2,3-dideoxy-dl-pent-2-enopyranos-4-ulose (3) and reduction in situ of the adduct afforded the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::c97cf562888f53ad443ba5dc6b3d684e
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3027650
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3027650