ChemInform Abstract: Synthesis of (Arylamido)pyrrolidinone Libraries Through Ritter-Type Cascade Reactions of Dihydroxylactams

The Ritter‐type reaction of arylnitriles and N‐acyliminium ions, generated in situ from dihydroxy‐γ‐lactams gives tetrahydropyrrolooxazolones in excellent yields.

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Veröffentlicht in:ChemInform 2015-12, Vol.47 (1), p.no-no
Hauptverfasser: Wu, Peng, Petersen, Michael Aaxman, Petersen, Rico, Rasmussen, Martin Ohsten, Bonnet, Karine, Nielsen, Thomas E., Clausen, Mads H.
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container_issue 1
container_start_page no
container_title ChemInform
container_volume 47
creator Wu, Peng
Petersen, Michael Aaxman
Petersen, Rico
Rasmussen, Martin Ohsten
Bonnet, Karine
Nielsen, Thomas E.
Clausen, Mads H.
description The Ritter‐type reaction of arylnitriles and N‐acyliminium ions, generated in situ from dihydroxy‐γ‐lactams gives tetrahydropyrrolooxazolones in excellent yields.
doi_str_mv 10.1002/chin.201601113
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subjects cascade reactions
cascade reactions, domino reactions, tandem reactions
domino reactions
fused pyrrole derivatives
pyrrole derivatives
tandem reactions
title ChemInform Abstract: Synthesis of (Arylamido)pyrrolidinone Libraries Through Ritter-Type Cascade Reactions of Dihydroxylactams
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