Zobrazeno 1 - 10 of 58 pro vyhledávání: '"Paul Hume"'
1
Helical thienothiophene (TT) and benzothieno–benzothiophene (BTBT) derivatives: synthesis, structural characterization and semiconducting properties
Autor: Maurizio Mastropasqua Talamo, Flavia Pop, Paul Hume, Mamatimin Abbas, Guillaume Wantz, Narcis Avarvari
Publikováno v: Journal of Materials Chemistry C. 10:8034-8042
A double helicenic benzothieno–benzothiophene derivative, showing homochiral layers of MM and PP enantiomers in the single crystal phase, behaves as a p-type semiconductor in thin-film OFET devices fabricated by both spin coating and evaporation.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bb15f8fc9bf8920155cb29ebb8332f02
https://doi.org/10.1039/d2tc00861k
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3
Direct alpha-Amination of Amides and Lactams Enabled by the (3+2) Vinyl Azide-Enolate Cycloaddition Manifold
Autor: Joseph Bell-Tyrer, Paul Hume, Phillip Grant, Margaret Brimble, Daniel Furkert
Direct alpha-amination of carbonyl compounds remains an important yet synthetically challenging transformation. Here we report a solution for direct alpha-amination of amides and lactams, identified through fundamental exploration of (3+2) vinyl azid
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b137b5046360e4db9914e74222d6e76
https://doi.org/10.26434/chemrxiv-2022-cf0c3-v2
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4
Ene-gamma-lactam synthesis via (3+2) vinyl azide-enolate cycloaddition: Enolate addition to vinyl triazolinone intermediates
Autor: Joseph Bell-Tyrer, Paul Hume, Margaret Brimble, Daniel Furkert
Vinyl azides have undergone a recent renaissance as versatile synthetic reagents, however their reactivity as 1,3-dipoles in (3+2) cycloadditions remains underexplored. Here the synthesis of ene-gamma-lactam scaffolds via (3+2) cycloaddition of alpha
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b2ed38cdde5cacfaa9303cd52bea6aa0
https://doi.org/10.26434/chemrxiv-2022-dhhj9
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