Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Guy V. Lamoureux"'
Autor:
Katherine Chaves-Carballo, Guy V. Lamoureux, Alice L. Perez, Alexandre Bella Cruz, Valdir Cechinel Filho
Publikováno v:
RSC Advances. 12:18507-18523
The development of new antibiotics and inexpensive antifungals is an important field of research. Based on the privileged pharmacophore of lawsone, a series of phenolic ether derivatives of 1,4-naphthoquinone were synthesized easily in one step in re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62ebdd3b90b264cc4e9773be4f6accc8
https://doi.org/10.1039/d2ra01814d
https://doi.org/10.1039/d2ra01814d
Autor:
Guy V. Lamoureux, George M. Whitesides
Publikováno v:
The Journal of Organic Chemistry. 58:633-641
Several dithiols have been prepared that are useful for the reduction of disulfides in aqueous solution. The reduction potential of these dithiols have been determined from the measurement of the equilibrium constant of thiol/disulfide interchange wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82bba8c6e5c6f74d9120969c27d1af3b
https://doi.org/10.1021/jo00055a015
https://doi.org/10.1021/jo00055a015
Autor:
George M. Whitesides, Guy V. Lamoureux
Publikováno v:
ChemInform. 24
Several dithiols have been prepared that are useful for the reduction of disulfides in aqueous solution. The reduction potential of these dithiols have been determined from the measurement of the equilibrium constant of thiol/disulfide interchange wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::951eb17ef698ba4fcdf92c4b2750f242
https://doi.org/10.1002/chin.199332125
https://doi.org/10.1002/chin.199332125
Publisher Summary This chapter describes the reagents that reduce disulfide bonds, under nondenaturing conditions at pH 7, faster than does dithiothreitol (DTT) by a factor of ∼5–7. Dithiothreitol and 2-mercaptoethanol (ME) are the most commonly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4295b68d3329a7cb9d6396ab5e273c3f
https://doi.org/10.1016/0076-6879(95)51119-9
https://doi.org/10.1016/0076-6879(95)51119-9
Publikováno v:
Canadian Journal of Chemistry. 64:520-522
The conversion of β-diketones to the corresponding β-chloro-α,β-unsaturated ketones is facilitated by using lithium hydride as a base and phenyl dichlorophosphate as an activating agent.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0a9d4a8c1b55aa0fe73e528ad7c4efb
https://doi.org/10.1139/v86-082
https://doi.org/10.1139/v86-082