Ugi post-condensation copper-triggered oxidative cascade towards pyrazoles

Pyrazolidinones were prepared in a two-step sequence starting from α-hydrazonocarboxylic acids. After a four-component Ugi coupling, the resulting hydrazone was engaged in a copper triggered [3 + 2] cycloaddition/aerobic oxidation cascade.

Bibliographic Details
Main Authors: Aurélie Dos Santos, Laurent El Kaim, Laurence Grimaud, Caroline Ronsseray
Format: Article
Language:English
Published: Beilstein-Institut 2011-09-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.7.153
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author Aurélie Dos Santos
Laurent El Kaim
Laurence Grimaud
Caroline Ronsseray
author_facet Aurélie Dos Santos
Laurent El Kaim
Laurence Grimaud
Caroline Ronsseray
author_sort Aurélie Dos Santos
collection DOAJ
description Pyrazolidinones were prepared in a two-step sequence starting from α-hydrazonocarboxylic acids. After a four-component Ugi coupling, the resulting hydrazone was engaged in a copper triggered [3 + 2] cycloaddition/aerobic oxidation cascade.
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spelling doaj.art-128760f5c20d4820b9e4b57d4a909ab32022-12-21T23:47:09ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972011-09-01711310131410.3762/bjoc.7.1531860-5397-7-153Ugi post-condensation copper-triggered oxidative cascade towards pyrazolesAurélie Dos Santos0Laurent El Kaim1Laurence Grimaud2Caroline Ronsseray3Laboratoire Chimie et Procédés, Laboratoire Chimie et procédés, UMR 7652-DCSO-CNRS- ENSTA-École Polytechnique, École Nationale Supérieure de Techniques Avancées, 32 Bd Victor, Paris 75015, FranceLaboratoire Chimie et Procédés, Laboratoire Chimie et procédés, UMR 7652-DCSO-CNRS- ENSTA-École Polytechnique, École Nationale Supérieure de Techniques Avancées, 32 Bd Victor, Paris 75015, FranceLaboratoire Chimie et Procédés, Laboratoire Chimie et procédés, UMR 7652-DCSO-CNRS- ENSTA-École Polytechnique, École Nationale Supérieure de Techniques Avancées, 32 Bd Victor, Paris 75015, FranceLaboratoire Chimie et Procédés, Laboratoire Chimie et procédés, UMR 7652-DCSO-CNRS- ENSTA-École Polytechnique, École Nationale Supérieure de Techniques Avancées, 32 Bd Victor, Paris 75015, FrancePyrazolidinones were prepared in a two-step sequence starting from α-hydrazonocarboxylic acids. After a four-component Ugi coupling, the resulting hydrazone was engaged in a copper triggered [3 + 2] cycloaddition/aerobic oxidation cascade.https://doi.org/10.3762/bjoc.7.153aerobic oxidationcopper(II)[3 + 2] cycloadditionhydrazoneisocyanidepyrazolidinone
spellingShingle Aurélie Dos Santos
Laurent El Kaim
Laurence Grimaud
Caroline Ronsseray
Ugi post-condensation copper-triggered oxidative cascade towards pyrazoles
Beilstein Journal of Organic Chemistry
aerobic oxidation
copper(II)
[3 + 2] cycloaddition
hydrazone
isocyanide
pyrazolidinone
title Ugi post-condensation copper-triggered oxidative cascade towards pyrazoles
title_full Ugi post-condensation copper-triggered oxidative cascade towards pyrazoles
title_fullStr Ugi post-condensation copper-triggered oxidative cascade towards pyrazoles
title_full_unstemmed Ugi post-condensation copper-triggered oxidative cascade towards pyrazoles
title_short Ugi post-condensation copper-triggered oxidative cascade towards pyrazoles
title_sort ugi post condensation copper triggered oxidative cascade towards pyrazoles
topic aerobic oxidation
copper(II)
[3 + 2] cycloaddition
hydrazone
isocyanide
pyrazolidinone
url https://doi.org/10.3762/bjoc.7.153
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