Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Randolph Escobar"'
Autor:
Cameron H. Chrisman, Max Kudisch, Katherine O. Puffer, Trevor K. Stewart, Yisrael M. L. Lamb, Chern-Hooi Lim, Randolph Escobar, Pall Thordarson, Jeffrey W. Johannes, Garret M. Miyake
Publikováno v:
Journal of the American Chemical Society.
Autor:
Cameron Chrisman, Max Kudisch, Katherine Puffer, Trevor Stewart, Yisrael Lamb, Chern-Hooi Lim, Randolph Escobar, Pall Thordarson, Jeffrey Johannes, Garret Miyake
Recent mechanistic studies of dual photoredox/Ni-catalyzed, light-driven cross-coupling reactions have found that the photocatalyst (PC) operates through either reductive quenching or energy transfer cycles. To date, reports invoking oxidative quench
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da79774a76fcf003ceb543a56588576a
https://doi.org/10.26434/chemrxiv-2023-x76sp
https://doi.org/10.26434/chemrxiv-2023-x76sp
Autor:
Jeffrey Johannes, Randolph Escobar
While carbon-heteroatom cross coupling reactions have been extensively studied, many methods are specific andlimited to a set of substrates or functional groups. Reported here is a method that allows for C-O, C-N and C-S cross coupling reactions unde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7ef636b64ca1c129b84696f05fdaa10
https://doi.org/10.26434/chemrxiv.9736049
https://doi.org/10.26434/chemrxiv.9736049
Autor:
John Porco, Scott Schaus, David Coker, Thomas Heavey, Randolph Escobar, Kyle Reichl, Michael Smith
Asymmetric synthesis of the biologically active xanthone dimer griffipavixanthone (GPX) is reported along with its absolute stereochemistry determination. Synthesis of the natural product is accomplished via dimerization of a p-quinone methide (p-QM)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b90891e7cecee6ba0317e61f83095bd
https://doi.org/10.26434/chemrxiv.7373969.v1
https://doi.org/10.26434/chemrxiv.7373969.v1