Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Desirée Steuernagel"'
Publikováno v:
Synlett. 33:1199-1204
The regioselectivity of the intramolecular cyclization of bifunctional α-phenyl alkenes can be controlled simply by the choice of the organic chromophore as the photocatalyst. The central photoredox catalytic reaction in both cases is a nucleophilic
Publikováno v:
Chemistry – A European Journal. 29
Autor:
Desirée Steuernagel, David Rombach, Daniel Sack, Martin Koos, Burkhard Luy, Hans‐Achim Wagenknecht
Publikováno v:
ChemPhotoChem, 7 (4), Art.Nr. e202200289
A new method activates CCl3F by means of photoredox catalysis and functionalizes alkenes by the CCl2F group. N-phenylphenothiazine is used as strongly reducing organophotocatalyst. The photoredox catalytic approach combines the productive disposal of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02a609ca1a863f4631698bd189c6c587
Publikováno v:
Chemistry – A European Journal, 29 (13), Art.-Nr.: e202203767
Acetals and ketals are among the most important protecting groups for carbonyl compounds. A new method for the acetalization and ketalization was developed by means of photoredox catalysis. The biscyanolated perylene bisimide is used as electron-poor