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Nucleophilic Isocyanation

[Image: see text] Isonitriles are frequently employed as both substrates for organic transformations and ligands for organometallic chemistry. However, despite the wide application of the isonitriles, their synthesis generally depends on the traditional dehydration of N-formamide. “Nucleophilic isoc...

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Autores principales: Yurino, Taiga, Ohkuma, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081272/
https://www.ncbi.nlm.nih.gov/pubmed/32201756
http://dx.doi.org/10.1021/acsomega.9b04073
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author Yurino, Taiga
Ohkuma, Takeshi
author_facet Yurino, Taiga
Ohkuma, Takeshi
author_sort Yurino, Taiga
collection PubMed
description [Image: see text] Isonitriles are frequently employed as both substrates for organic transformations and ligands for organometallic chemistry. However, despite the wide application of the isonitriles, their synthesis generally depends on the traditional dehydration of N-formamide. “Nucleophilic isocyanation” using cyanide as an N-nucleophile is another straightforward strategy affording the corresponding isonitriles. This method has been available since the 19th century but is still an immature procedure and is therefore more rarely used. In this review, we summarize the concepts and recent progress in nucleophilic isocyanation, including the relatively rare examples of catalytic isocyanation.
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spelling pubmed-70812722020-03-20 Nucleophilic Isocyanation Yurino, Taiga Ohkuma, Takeshi ACS Omega [Image: see text] Isonitriles are frequently employed as both substrates for organic transformations and ligands for organometallic chemistry. However, despite the wide application of the isonitriles, their synthesis generally depends on the traditional dehydration of N-formamide. “Nucleophilic isocyanation” using cyanide as an N-nucleophile is another straightforward strategy affording the corresponding isonitriles. This method has been available since the 19th century but is still an immature procedure and is therefore more rarely used. In this review, we summarize the concepts and recent progress in nucleophilic isocyanation, including the relatively rare examples of catalytic isocyanation. American Chemical Society 2020-03-09 /pmc/articles/PMC7081272/ /pubmed/32201756 http://dx.doi.org/10.1021/acsomega.9b04073 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Yurino, Taiga
Ohkuma, Takeshi
Nucleophilic Isocyanation
title Nucleophilic Isocyanation
title_full Nucleophilic Isocyanation
title_fullStr Nucleophilic Isocyanation
title_full_unstemmed Nucleophilic Isocyanation
title_short Nucleophilic Isocyanation
title_sort nucleophilic isocyanation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081272/
https://www.ncbi.nlm.nih.gov/pubmed/32201756
http://dx.doi.org/10.1021/acsomega.9b04073
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