Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Christo S. Sevov"'
Autor:
Heather A. Hintz, Christo S. Sevov
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-7 (2022)
This work leverages substrate self-assembly at an electrode to promote selective substrate electrooxidation in the presence of oxidatively sensitive catalysts. This strategy is applied to decarboxylative coupling of carboxylic acids with olefins.
Externí odkaz:
https://doaj.org/article/55aa649424424e829d24176601c524e2
Autor:
Koen H. Hendriks, Sophia G. Robinson, Miles N. Braten, Christo S. Sevov, Brett A. Helms, Matthew S. Sigman, Shelley D. Minteer, Melanie S. Sanford
Publikováno v:
ACS Central Science, Vol 4, Iss 2, Pp 189-196 (2018)
Externí odkaz:
https://doaj.org/article/1b14e4b57fe14301a65dca0e0bdd9173
Publikováno v:
ACS Energy Letters. 7:3337-3344
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::930e6137ed597452b55a56430e58db3f
https://doi.org/10.1021/acsenergylett.2c01794
https://doi.org/10.1021/acsenergylett.2c01794
Publikováno v:
ACS Catal
Electroreductive cross-electrophile coupling (eXEC) represents an attractive approach for the direct C-C coupling of two electrophiles but generally suffers from limited scope compared to reactions with chemical reductants. This work demonstrates tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d113256ace260cb726d94c43b20160c0
https://doi.org/10.1021/acscatal.1c05144
https://doi.org/10.1021/acscatal.1c05144
Autor:
Radoslav Z. Pavlović, Lei Zhiquan, Tyler J. Finnegan, Christopher A. Waudby, Xiuze Wang, Vageesha W. Liyana Gunawardana, Xingrong Zhu, Curt M. Wong, Taylor Hamby, Curtis E. Moore, Nicole Hoefer, David W. McComb, Christo S. Sevov, Jovica D. Badjić
Publikováno v:
Angewandte Chemie International Edition. 61
In this study, we describe a synthetic method for incorporating arenes into closed tubes that we name capsularenes. First, we prepared vase-shaped molecular baskets 4-7. The baskets comprise a benzene base fused to three bicycle[2.2.1]heptane rings t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::058e8d02a83d7d99b7cac34e1b2a3515
https://doi.org/10.1002/anie.202211304
https://doi.org/10.1002/anie.202211304
Publikováno v:
J Am Chem Soc
Simple copper salts serve as catalysts to effect C–X bond-forming reactions in some of the most utilized transformations in synthesis, including the oxidative coupling of aryl boronic acids and amines. However, these Chan–Lam coupling reactions h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1da321905d46a877b495cbef29380f0
https://doi.org/10.1021/jacs.1c02103
https://doi.org/10.1021/jacs.1c02103
Autor:
Curt M. Wong, Christo S. Sevov
Publikováno v:
ACS Energy Letters. :1271-1279
Large-scale integration of renewable energies into the electrical grid will remain limited until high-capacity storage systems are developed to modulate the intermittency of harvestable sources. Th...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::138b4e5269e835e49e6579526b61cf1d
https://doi.org/10.1021/acsenergylett.1c00143
https://doi.org/10.1021/acsenergylett.1c00143
Publikováno v:
Science
Cross-electrophile coupling (XEC) reactions of aryl and alkyl electrophiles are appealing but limited to specific substrate classes. Here, we report electroreductive XEC of previously incompatible electrophiles including tertiary alkyl bromides, aryl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a5df9c28d3a994d285ba68ae403398f
https://pubmed.ncbi.nlm.nih.gov/35446658
https://pubmed.ncbi.nlm.nih.gov/35446658
Publikováno v:
Journal of the American Chemical Society. 142:5884-5893
Cross-electrophile coupling (XEC) of alkyl and aryl halides promoted by electrochemistry represents an attractive alternative to conventional methods that require stoichiometric quantities of high-energy reductants. Most importantly, electroreduction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6a852684b098da66c303b8ac6095be0
https://doi.org/10.1021/jacs.0c01475
https://doi.org/10.1021/jacs.0c01475
Publikováno v:
Journal of the American Chemical Society. 142:3024-3031
The direct and scalable electroreduction of triphenylphosphine oxide (TPPO)-the stoichiometric byproduct of some of the most common synthetic organic reactions-to triphenylphosphine (TPP) remains an unmet challenge that would dramatically reduce the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa0fa93c0c699e09921ef9c9c18e6463
https://doi.org/10.1021/jacs.9b12112
https://doi.org/10.1021/jacs.9b12112