Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Frederick A. Luzzio"'
Publikováno v:
ARKIVOC, Vol 2019, Iss 5, Pp 298-306 (2019)
Externí odkaz:
https://doaj.org/article/5d15c741caf841579a95549ff38634d9
Autor:
Bernard L. Adjei, Frederick A. Luzzio
Publikováno v:
Molecules, Vol 27, Iss 2, p 548 (2022)
A systematic study of the oxidation of 3-hydroxy-2-substituted isoindolin-1-ones (hydroxylactams) and their conversion to the corresponding phthalimides was undertaken using three oxidants. Of special interest was the introduction of nickel peroxide
Externí odkaz:
https://doaj.org/article/c65c4f4c5bbf4a588492de790b764c4f
Autor:
Frederick A. Luzzio
Publikováno v:
Comprehensive Heterocyclic Chemistry IV ISBN: 9780128186565
Comprehensive Heterocyclic Chemistry IV
Comprehensive Heterocyclic Chemistry IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e590ce387ad435ba8799390f827c6bb1
https://doi.org/10.1016/b978-0-12-818655-8.00049-4
https://doi.org/10.1016/b978-0-12-818655-8.00049-4
Publikováno v:
ARKIVOC, Vol 2019, Iss 5, Pp 298-306 (2019)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6165fb900a9ef206c058d1f5b16c4f5b
https://doi.org/10.24820/ark.5550190.p010.809
https://doi.org/10.24820/ark.5550190.p010.809
Autor:
Frederick A. Luzzio, Paige J. Monsen
Publikováno v:
Journal of Chemical Education. 96:992-997
A laboratory experiment is detailed that entails the separation and derivatization of the artificial sweetener sucralose from a commercially available sweetener mixture. The experiment utilizes 1 g...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e901e80cb303e242949b6440feedf65
https://doi.org/10.1021/acs.jchemed.8b00413
https://doi.org/10.1021/acs.jchemed.8b00413
Publikováno v:
MedChemComm. 10:268-279
Several ‘second-generation’ click inhibitors of the multi-species biofilm propagated by the adherence of the oral pathogen Porphyromonas gingivalis to Streptococcus gordonii were synthesized and evaluated. The design of the structures was based o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a55de2c4ad0a9783e24aad53ccc8d36
https://doi.org/10.1039/c8md00405f
https://doi.org/10.1039/c8md00405f
Autor:
Paige J. Monsen, Frederick A. Luzzio
Publikováno v:
Journal of Natural Products. 81:1905-1909
Annonacin (1) was isolated from the North American pawpaw (Asimina triloba), as reported earlier from these laboratories. Natural 1 was submitted to the rat aortic ring bioassay for evaluation of antiangiogenic activity and was found to inhibit micro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a600e58d78c2532066cf3a445a2635c6
https://doi.org/10.1021/acs.jnatprod.8b00284
https://doi.org/10.1021/acs.jnatprod.8b00284
Publikováno v:
Tetrahedron Letters. 58:3730-3733
The interchangeability of the isoindolinone group as a nitrogen protecting group for amino acid intermediates is demonstrated by the preparation of several natural and unnatural α-amino acid derivatives using a two-carbon N-isoindolinone (phthalimid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef66f5261046d41ee4d0e77d5a77cd29
https://doi.org/10.1016/j.tetlet.2017.08.032
https://doi.org/10.1016/j.tetlet.2017.08.032
Autor:
Frederick A. Luzzio, Pravin C. Patil
Publikováno v:
Synlett. 28:1729-1732
A novel tert-butyl 2-(1-oxoisoindolin-2-yl)acetate derivative is selectively alkylated with propargyl bromide in the presence of lithium hexamethyldisilazide. After removal of the tert-butyl protecting group, the resulting N-isoindolinyl (ethynylalan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::741972fa1718e81f4b8bee841245e13f
https://doi.org/10.1055/s-0036-1588510
https://doi.org/10.1055/s-0036-1588510
Publikováno v:
ARKIVOC, Vol 2017, Iss 1, Pp 117-147 (2017)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0437a2cbb8973e930511300c76cd7b8d
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p009.917
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p009.917