Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Nicholas R. Treich"'
Synthesis and characterization of chiral and achiral diamines containing one or two BODIPY molecules
Publikováno v:
New Journal of Chemistry. 41:14370-14378
The synthesis and characterization of one or two BODIPY fragments appended to four new chiral and one new achiral diamines is described. All of the examined BODIPY-appended diamines exhibit a quasireversible-irreversible reduction, with two reduction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99cd916284c658e56336dc57cef097f0
https://doi.org/10.1039/c7nj02670f
https://doi.org/10.1039/c7nj02670f
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 47(11)
Hydride transfer promoted by the coordination of a substrate molecule to a Lewis acid is a critical step in many catalytic transformations. This computational study investigates the nature of the interaction between a polar substrate molecule and a L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9db0f3dbbe8c4e4f655fafd4afb639d
https://pubmed.ncbi.nlm.nih.gov/29464246
https://pubmed.ncbi.nlm.nih.gov/29464246
Publikováno v:
Israel Journal of Chemistry. 55:226-234
The steric bulk of reducing agents has been widely employed in the generation of chiral centers and selective reductions of organic compounds, but reports addressing the quantification of the steric bulk surrounding the main group hydride have been v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f9924f52337b4ed5b609c91d5e5c86e
https://doi.org/10.1002/ijch.201400137
https://doi.org/10.1002/ijch.201400137