Articles with "aryl rearrangement" as a keyword



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Photoinduced transition-metal- and external-photosensitizer-free intramolecular aryl rearrangement via C(Ar)–O bond cleavage† †Electronic supplementary information (ESI) available. See DOI: 10.1039/d0sc01585g

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Published in 2020 at "Chemical Science"

DOI: 10.1039/d0sc01585g

Abstract: “We report a protocol for photoinduced transition-metal- and external-photocatalyst-free intramolecular heteroaryl/aryl rearrangement reactions of 2-heteroaryl/aryloxybenzaldehydes. The protocol was compatible with a variety of functionalities. read more here.

Keywords: transition metal; metal external; photoinduced transition; free intramolecular ... See more keywords
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Nickel-catalyzed 1,4-aryl rearrangement of aryl N-benzylimidates via C-O and C-H bond cleavage.

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Published in 2022 at "Chemical communications"

DOI: 10.1039/d2cc02355e

Abstract: We report herein that nickel-catalyzed reaction of aryl imidates bearing an N-benzyl group results in 1,4-migration of an O-aryl group via the cleavage of C-O and C-H bonds. This protocol allows for the benzylic C-H… read more here.

Keywords: cleavage; aryl; nickel catalyzed; catalyzed aryl ... See more keywords