Výsledky vyhledávání - "E. L. Michelotti"

Antifungal properties of taxol and various analogues

Autor: D H Young, N E Krauss, Charles S. Swindell, E L Michelotti

Publikováno v: Experientia. 48:882-885

The antimitotic agent taxol was tested for toxicity towards fungi from different taxonomic groups and found to be particularly active against oomycete fungi. In germinating zoospore cysts of the oomycete Phytophthora capsici the mechanism of action o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d226caf3e5c0ec9220781d9d89bdefa
https://doi.org/10.1007/bf02118425

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Solid phase vs. solution phase differential behavior: formation of a salicylate structure from a malondialdehyde moiety

Autor: J I, Borrell, J, Teixidó, E, Schuler, E L, Michelotti

Publikováno v: Molecular diversity. 5(3)

Treatment of 2, solid supported synthetic equivalent of 3-formylchromone (4), and ethyl acetoacetate affords the salicylate structure 8 instead of the previously reported isophtalate 7. This is the first formation of a salicylate by a double carbonyl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::690f63215ea53b42c83f4d7463e231b7
https://pubmed.ncbi.nlm.nih.gov/12197073

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Effect of side-chain shortening on the physiologic properties of bile acids: Hepatic transport and effect on biliary secretion of 23-nor-ursodeoxycholate in rodents

Autor: E L Michelotti, Lee R. Hagey, Alan F. Hofmann, Devorah Gurantz, Joseph H. Steinbach, Y B Yoon

Publikováno v: Gastroenterology. 90:837-852

To define whether side-chain length influences the physiologic properties of bile acids, nor-ursodeoxycholate (nor-UDC), the C23-nor derivative of ursodeoxycholate (UDC), was synthesized in both nonradioactive and radioactive forms (23-14C). Its hepa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::807d7e01e037173ff0f18150d964cc90
https://doi.org/10.1016/0016-5085(86)90859-0

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Stereospecific Synthesis of 4,8-Dimethylspiro(4,5)-deca-7-ene-1,6-dione A Synthetic Route to the Acoranes

Autor: E. L. Michelotti, E. L. Sanchez

Publikováno v: Zeitschrift für Naturforschung B. 38:497-500

A stereospecific synthesis of 4,8-dimethylspiro(4,5)-deca-7-ene-1,6-dione from 4,7-dimethylcoumarine in high yield is reported. The configuration of this product is established according to its 1H NMR and 13C NMR data.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::20fd4163201d08884b283ebd9deffe45
https://doi.org/10.1515/znb-1983-0417

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