author_facet Johnson, Tarn C
Marsden, Stephen P
Johnson, Tarn C
Marsden, Stephen P
author Johnson, Tarn C
Marsden, Stephen P
spellingShingle Johnson, Tarn C
Marsden, Stephen P
Beilstein Journal of Organic Chemistry
A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
Organic Chemistry
author_sort johnson, tarn c
spelling Johnson, Tarn C Marsden, Stephen P 1860-5397 Beilstein Institut Organic Chemistry http://dx.doi.org/10.3762/bjoc.12.1 <jats:p>A convenient, one-pot, two-component synthesis of 2-(1-amidoalkyl)pyridines is reported, based upon the substitution of suitably-activated pyridine <jats:italic>N</jats:italic>-oxides by azlactone nucleophiles, followed by decarboxylative azlactone ring-opening. The synthesis obviates the need for precious metal catalysts to achieve a formal enolate arylation reaction, and constitutes a formally ‘umpoled’ approach to this valuable class of bioactive structures.</jats:p> A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines Beilstein Journal of Organic Chemistry
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title A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_unstemmed A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_full A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_fullStr A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_full_unstemmed A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_short A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_sort a convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
topic Organic Chemistry
url http://dx.doi.org/10.3762/bjoc.12.1
publishDate 2016
physical 1-4
description <jats:p>A convenient, one-pot, two-component synthesis of 2-(1-amidoalkyl)pyridines is reported, based upon the substitution of suitably-activated pyridine <jats:italic>N</jats:italic>-oxides by azlactone nucleophiles, followed by decarboxylative azlactone ring-opening. The synthesis obviates the need for precious metal catalysts to achieve a formal enolate arylation reaction, and constitutes a formally ‘umpoled’ approach to this valuable class of bioactive structures.</jats:p>
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author Johnson, Tarn C, Marsden, Stephen P
author_facet Johnson, Tarn C, Marsden, Stephen P, Johnson, Tarn C, Marsden, Stephen P
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description <jats:p>A convenient, one-pot, two-component synthesis of 2-(1-amidoalkyl)pyridines is reported, based upon the substitution of suitably-activated pyridine <jats:italic>N</jats:italic>-oxides by azlactone nucleophiles, followed by decarboxylative azlactone ring-opening. The synthesis obviates the need for precious metal catalysts to achieve a formal enolate arylation reaction, and constitutes a formally ‘umpoled’ approach to this valuable class of bioactive structures.</jats:p>
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series Beilstein Journal of Organic Chemistry
source_id 49
spelling Johnson, Tarn C Marsden, Stephen P 1860-5397 Beilstein Institut Organic Chemistry http://dx.doi.org/10.3762/bjoc.12.1 <jats:p>A convenient, one-pot, two-component synthesis of 2-(1-amidoalkyl)pyridines is reported, based upon the substitution of suitably-activated pyridine <jats:italic>N</jats:italic>-oxides by azlactone nucleophiles, followed by decarboxylative azlactone ring-opening. The synthesis obviates the need for precious metal catalysts to achieve a formal enolate arylation reaction, and constitutes a formally ‘umpoled’ approach to this valuable class of bioactive structures.</jats:p> A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines Beilstein Journal of Organic Chemistry
spellingShingle Johnson, Tarn C, Marsden, Stephen P, Beilstein Journal of Organic Chemistry, A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines, Organic Chemistry
title A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_full A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_fullStr A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_full_unstemmed A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_short A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_sort a convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
title_unstemmed A convergent, umpoled synthesis of 2-(1-amidoalkyl)pyridines
topic Organic Chemistry
url http://dx.doi.org/10.3762/bjoc.12.1