Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Marisa Kozlowski"'
Autor:
Shelley Minteer, Jingguang Chen, Song Lin, Cathleen Crudden, Stefanie Dehnen, Prashant V. Kamat, Marisa Kozlowski, Géraldine Masson, Scott J. Miller
Publikováno v:
ACS Measurement Science Au, Vol 3, Iss 2, Pp 82-83 (2023)
Externí odkaz:
https://doaj.org/article/0821a1ef5a5d49239a53716d8c38577d
Autor:
Christopher Sojdak, Marisa Kozlowski
Publikováno v:
Organic letters. 24(45)
A method to cleave the C-C biaryl bond of binaphthyl derivatives under reductive conditions is described. Triflic acid employed together with a catalytic HAT reagent, 2-ethyl-9,10-dihydroxyanthracene, that is regenerated using H
Autor:
Marisa Kozlowski, Jingze Wu
Publikováno v:
Organic Letters. 25:907-911
Publikováno v:
Organic Letters. 24:7250-7254
Autor:
Marisa Kozlowski
Publikováno v:
Organic Letters. 24:7247-7249
Publikováno v:
The Journal of Organic Chemistry. 87:12507-12509
Autor:
Paige Piszel, Brandon Orzolek, Alyssa Olszewski, Madeline Rotella, Amanda Spiewak, Marisa Kozlowski, Daniel Weix
Protonation of C–M bonds and its microscopic reverse, metalation of C–H bonds, are fundamental steps in a variety of metal-catalyzed processes. As such, studies on protonation of C–M bonds can shed light on C–H activation. We present here stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53db89cc7e0da6644373b554de21c7dd
https://doi.org/10.26434/chemrxiv-2023-v13qq
https://doi.org/10.26434/chemrxiv-2023-v13qq
Publikováno v:
Chemistry – A European Journal. 29
Oxidative phenol coupling reduces reliance on halo/metalated substrates used in conventional redox neutral couplings. A new strategy for constructing polycyclic aromatic hydrocarbons (PAHs) that incorporates oxidative phenol coupling is outlined in a
Autor:
Jingze Wu, Marisa Kozlowski
Publikováno v:
ACS Catal
Phenols and their derivatives are the elementary building blocks for several classes of complex molecules that play essential roles in biological systems. Nature has devised methods to selectively couple phenolic compounds, and many efforts have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b41d22e3e6a549ddc0e1ccc4fd7e55ae
https://europepmc.org/articles/PMC9345132/
https://europepmc.org/articles/PMC9345132/
Vanadium-catalyzed intramolecular coupling of tethered phenols: Formation of phenol-dienone products
Autor:
Philip Gilmartin, Marisa Kozlowski
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3273524b3f085713d4cc27fa652b63a
https://doi.org/10.1021/scimeetings.0c07107
https://doi.org/10.1021/scimeetings.0c07107