Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sarah L. Skraba-Joiner"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2655-2663 (2019)
Arenes undergo rearrangement of phenyl, alkyl, halogen and other groups through the intermediacy of ipso arenium ions in which a proton is attached at the same carbon as the migrating substituent. Interconversions among the six quaterphenyl isomers h
Externí odkaz:
https://doaj.org/article/e586d8e0cadf49b6ab99044a765638b3
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2655-2663 (2019)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
Arenes undergo rearrangement of phenyl, alkyl, halogen and other groups through the intermediacy of ipso arenium ions in which a proton is attached at the same carbon as the migrating substituent. Interconversions among the six quaterphenyl isomers h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4f5551269b2ff03721336899d5b7dd3
https://doaj.org/article/e586d8e0cadf49b6ab99044a765638b3
https://doaj.org/article/e586d8e0cadf49b6ab99044a765638b3
Autor:
Tong Jin, Chao Liu, Tijana Rajh, Sarah L. Skraba-Joiner, Michael E. Louis, Sebastian A. Pantovich, Gonghu Li
Publikováno v:
Journal of Molecular Catalysis A: Chemical. 423:293-299
Hybrid photocatalysts consisting of molecular catalysts and solid-state surfaces have demonstrated great potential as robust and efficient systems in solar fuel production. Based on our prior work, we synthesized hybrid photocatalysts by depositing a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdf9fd7fae9c8b6b49c112d28f60d930
https://doi.org/10.1016/j.molcata.2016.07.019
https://doi.org/10.1016/j.molcata.2016.07.019
Publikováno v:
The Journal of Organic Chemistry. 80:11779-11787
The conceptual dehydrogenation of pericyclic reactions yields dehydropericyclic processes, which usually lead to strained or reactive intermediates. This is a simple scheme for inventing new chemical reactions. Computational results on two novel dehy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d97aec1fdf924ff792bbc6c997b66861
https://doi.org/10.1021/acs.joc.5b01488
https://doi.org/10.1021/acs.joc.5b01488
Publikováno v:
The Journal of Organic Chemistry. 80:9578-9583
In 1910, Scholl, Seer, and Weitzenbock reported the AlCl3-catalyzed cyclization of 1,1'-binaphthyl to perylene. We provide evidence that this classic organic name reaction proceeds through sequential and reversible formation of 1,2'- and 2,2'-binapht
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3767e8a9821d40e024f8cfe9b52a92b
https://doi.org/10.1021/acs.joc.5b01559
https://doi.org/10.1021/acs.joc.5b01559
Autor:
Richard P. Johnson, Sarah L. Skraba-Joiner, Zeinab G. Khalil, John A. Porco, Robert J. Capon, Tian Qin
Publikováno v:
Nature chemistry
Chiral, dimeric natural products containing complex structures and interesting biological properties have inspired chemists and biologists for decades. A seven step total synthesis of the axially chiral, dimeric tetrahydroxanthone natural product rug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfb3848b0094d03cde9c857fc17fd4d2
https://doi.org/10.1038/nchem.2173
https://doi.org/10.1038/nchem.2173
Publikováno v:
The Journal of organic chemistry. 82(24)
In 1 M triflic acid/dichloroethane, anthracene is protonated at C9, and the resulting 9-anthracenium ion is easily observed by NMR at ambient temperature. When heated as a dilute solution in triflic acid/dichloroethane, anthracene undergoes conversio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b98c677d953b43b96ad1c6bc76e1114
https://pubmed.ncbi.nlm.nih.gov/29134806
https://pubmed.ncbi.nlm.nih.gov/29134806
Autor:
Katharine J. Cahill, Alicia C. Voukides, Aida Ajaz, Rajesh Thamatam, Sarah L. Skraba-Joiner, Richard P. Johnson
Publikováno v:
Australian Journal of Chemistry. 67:1301
The pyrolysis of 2-ethynyltoluene, indene, fluorene, and related compounds has been studied by sealed tube microwave flash pyrolysis (MFP), in concert with modelling of putative mechanistic pathways by density functional theory (DFT) computations. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7d1b3872ac3486f15dff580a7da88f6
https://doi.org/10.1071/ch14238
https://doi.org/10.1071/ch14238