Cargando…
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...
Autores principales: | , |
---|---|
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 |
_version_ | 1783508143137882112 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7081272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT yurinotaiga nucleophilicisocyanation AT ohkumatakeshi nucleophilicisocyanation |