Multiple Isocyanide insertions promoted by protic and Lewis acids

The protonation, or Lewis Acid complexation, of electrophiles can trigger the sequential insertion of two or more isocyanides resulting in valuable iminonitriles or heterocycles. The number of insertions is controlled by the nature of the alkyl- or arylisocyanide and by the presence of a proximal nu...

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Main Authors: John Kornfeind, Fraser F. Fleming
Format: Article
Language:English
Published: Elsevier 2024-03-01
Series:Tetrahedron Chem
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666951X23000220
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author John Kornfeind
Fraser F. Fleming
author_facet John Kornfeind
Fraser F. Fleming
author_sort John Kornfeind
collection DOAJ
description The protonation, or Lewis Acid complexation, of electrophiles can trigger the sequential insertion of two or more isocyanides resulting in valuable iminonitriles or heterocycles. The number of insertions is controlled by the nature of the alkyl- or arylisocyanide and by the presence of a proximal nucleophile capable of attacking the intermediate nitrilium; loss of an alkyl group from the nitrilium or attack by a nucleophile terminates further isocyanide insertions. The mechanistic survey of protic and Lewis acid-promoted isocyanide insertions aims to provide a fundamental understanding of the reactivity and selectivity to facilitate synthetic applications. The review is structured with an introductory overview followed by a mechanistic analysis before moving to a survey of double insertions, which are the most prevalent, then triple insertions; the survey concludes with the sole example of a quadruple insertion. The hope is that the insight contained in the review will aid in applying protic and Lewis acid-activated isocyanide insertions to prepare an array of complex heterocycles.
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spelling doaj.art-7a09947523624fd4bb1143f4f0f8d4bb2024-03-24T07:02:04ZengElsevierTetrahedron Chem2666-951X2024-03-019100056Multiple Isocyanide insertions promoted by protic and Lewis acidsJohn Kornfeind0Fraser F. Fleming1Department of Chemistry, Drexel University, 3401 Chestnut St., Philadelphia, PA, USA 19104Corresponding author.; Department of Chemistry, Drexel University, 3401 Chestnut St., Philadelphia, PA, USA 19104The protonation, or Lewis Acid complexation, of electrophiles can trigger the sequential insertion of two or more isocyanides resulting in valuable iminonitriles or heterocycles. The number of insertions is controlled by the nature of the alkyl- or arylisocyanide and by the presence of a proximal nucleophile capable of attacking the intermediate nitrilium; loss of an alkyl group from the nitrilium or attack by a nucleophile terminates further isocyanide insertions. The mechanistic survey of protic and Lewis acid-promoted isocyanide insertions aims to provide a fundamental understanding of the reactivity and selectivity to facilitate synthetic applications. The review is structured with an introductory overview followed by a mechanistic analysis before moving to a survey of double insertions, which are the most prevalent, then triple insertions; the survey concludes with the sole example of a quadruple insertion. The hope is that the insight contained in the review will aid in applying protic and Lewis acid-activated isocyanide insertions to prepare an array of complex heterocycles.http://www.sciencedirect.com/science/article/pii/S2666951X23000220IsocyanideInsertionsCyclizationsLewis acidsCascades
spellingShingle John Kornfeind
Fraser F. Fleming
Multiple Isocyanide insertions promoted by protic and Lewis acids
Tetrahedron Chem
Isocyanide
Insertions
Cyclizations
Lewis acids
Cascades
title Multiple Isocyanide insertions promoted by protic and Lewis acids
title_full Multiple Isocyanide insertions promoted by protic and Lewis acids
title_fullStr Multiple Isocyanide insertions promoted by protic and Lewis acids
title_full_unstemmed Multiple Isocyanide insertions promoted by protic and Lewis acids
title_short Multiple Isocyanide insertions promoted by protic and Lewis acids
title_sort multiple isocyanide insertions promoted by protic and lewis acids
topic Isocyanide
Insertions
Cyclizations
Lewis acids
Cascades
url http://www.sciencedirect.com/science/article/pii/S2666951X23000220
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