Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Nicole D. Bartolo"'
Publikováno v:
Subterranean Biology, Vol 13, Iss 0, Pp 35-44 (2014)
The blind Mexican tetra fish, Astyanax mexicanus, has become the most influential model for research of cave adapted organisms. Many authors assume that the Sierra de Guatemala populations and the Sierra de El Abra populations are derived from two in
Externí odkaz:
https://doaj.org/article/024651fe88c54241b0211651e431b9ac
Publikováno v:
European Journal of Taxonomy, Vol 0, Iss 156 (2015)
Anelpistina taninuli sp. nov. (Insecta: Zygentoma: Nicoletiidae), a species from Taninul, Sierra de El Abra, San Luis Potosi, Mexico, is described. We also report the 16S rRNA sequence of this new species.
Externí odkaz:
https://doaj.org/article/aff9bf8f58474e0795794d74ec85d7af
Autor:
Nicole D. Bartolo, Niall Mortimer, Mariah A. Manter, Nicholas Sanchez, Misha Riley, Tiernan T. O’Malley, Jacob M. Hooker
Publikováno v:
ACS Chemical Neuroscience. 13:3641-3660
Activation of microglial cells accompanies the progression of many neurodegenerative disorders, including Alzheimer's disease (AD). Development of molecular imaging tools specific to microglia can help elucidate the mechanism through which microglia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11ffaad589f2d165d147e9fcb4819301
https://doi.org/10.1021/acschemneuro.2c00607
https://doi.org/10.1021/acschemneuro.2c00607
Autor:
Nicole D. Bartolo, Krystyna M. Demkiw, Jacquelyne A. Read, Elizabeth M. Valentín, Yingying Yang, Alexandra M. Dillon, Chunhua T. Hu, Michael D. Ward, K. A. Woerpel
Publikováno v:
J Org Chem
The additions of the highly reactive reagent, allylmagnesium halide, to α-substituted acyclic chiral ketones proceeded with high stereoselectivity. The stereoselectivity cannot be analyzed by conventional stereochemical models because these reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa80a442430233715ec40c60e9f63359
https://doi.org/10.1021/acs.joc.1c02844
https://doi.org/10.1021/acs.joc.1c02844
Autor:
Nicole D. Bartolo, Sarah E. Reid, Hema S. Krishnan, Azra Haseki, Muthukrishnan Renganathan, Tally M. Largent-Milnes, Braxton A. Norwood, Marco L. Loggia, Jacob M. Hooker
Publikováno v:
ACS chemical neuroscience. 13(24)
Voltage-gated sodium channels (Na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::143513fb1aeceed44f8d0592161670df
https://pubmed.ncbi.nlm.nih.gov/36472927
https://pubmed.ncbi.nlm.nih.gov/36472927
Autor:
Nicole D. Bartolo, K. A. Woerpel
Publikováno v:
J Org Chem
A radical clock system was developed to investigate single-electron transfer (SET) in the reactions of organomagnesium reagents with carbonyl compounds. The fluorenylcyclopropyl radical clock was selected because it is the fastest known radical clock
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfdc8d8a00432efcc8adaf9aca79ed43
https://doi.org/10.1021/acs.joc.0c00481
https://doi.org/10.1021/acs.joc.0c00481
Autor:
Nicole D. Bartolo, Krystyna M. Demkiw, Alya A. Arabi, Chunhua T. Hu, Elizabeth M. Valentín, K. A. Woerpel
Publikováno v:
J Org Chem
The stereoselectivities of reactions of allylmagnesium reagents with chiral ketones cannot be easily explained by stereochemical models. Competition experiments indicate that the complexation step is not reversible, so nucleophiles cannot access the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01506997b7dcf820b92dd28c56db49cc
https://pubmed.ncbi.nlm.nih.gov/33978419
https://pubmed.ncbi.nlm.nih.gov/33978419
Publikováno v:
Chem Rev
This review describes the additions of allylmagnesium reagents to carbonyl compounds and to imines, focusing on the differences in reactivity between allylmagnesium halides and other Grignard reagents. In many cases, allylmagnesium reagents either re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0471e3f3b008c97f717bd72e1dd11eb6
https://europepmc.org/articles/PMC7018623/
https://europepmc.org/articles/PMC7018623/
Publikováno v:
Synthesis. 51:296-302
The chelation-control model is used to predict stereochemical outcomes of many organometallic reactions. Diastereoselectivity arises due to reaction with a chelated intermediate with sterically differentiated faces. Earlier studies with dimethylmagne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d4c6956e2eaf0da3126e3ccf67a5365
https://doi.org/10.1055/s-0037-1610381
https://doi.org/10.1055/s-0037-1610381
Publikováno v:
Synthesis. 49:3237-3246
The additions of allylmagnesium reagents to carbonyl compounds are important methods in synthetic organic chemistry, but the mechanisms of these reactions are likely to be distinct from mechanisms followed by other organomagnesium reagents. Additions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c1e5f67fb9c13d9242323425759552e
https://doi.org/10.1055/s-0036-1588427
https://doi.org/10.1055/s-0036-1588427