ChemInform Abstract: Regioselective Synthesis of 3‐Hydroxy‐4,5‐alkyl‐Substituted Pyridines Using 1,3‐Enynes as Alkynes Surrogates

ChemInform Abstract: Regioselective Synthesis of 3‐Hydroxy‐4,5‐alkyl‐Substituted Pyridines Using 1,3‐Enynes as Alkynes Surrogates

1,3‐enynes are convenient surrogates of internal alkynes bearing two alkyl substituents in their nickel‐catalyzed [4 + 2] cycloaddition with 3‐azetidinones.

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Veröffentlicht in:ChemInform 2016-08, Vol.47 (34), p.no-no
Hauptverfasser: Barday, Manuel, Ho, Kelvin Y. T., Halsall, Christopher T., Aissa, Christophe
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Sprache:eng
Schlagworte:
cycloaddition reactions
pyridine derivatives
reduction, hydrogenation
regioselective reactions
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container_title ChemInform
container_volume 47
creator Barday, Manuel
Ho, Kelvin Y. T.
Halsall, Christopher T.
Aissa, Christophe
description 1,3‐enynes are convenient surrogates of internal alkynes bearing two alkyl substituents in their nickel‐catalyzed [4 + 2] cycloaddition with 3‐azetidinones.
doi_str_mv 10.1002/chin.201634144
format Article
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source Wiley Online Library Journals Frontfile Complete
subjects cycloaddition reactions
pyridine derivatives
reduction, hydrogenation
regioselective reactions
title ChemInform Abstract: Regioselective Synthesis of 3‐Hydroxy‐4,5‐alkyl‐Substituted Pyridines Using 1,3‐Enynes as Alkynes Surrogates
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