N-Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations

In the field of organosulfur chemistry, sulfenylating agents are an important key in C–S bond formation strategies. Among various organosulfur precursors, N-sulfenylsuccinimide/phthalimide derivatives have shown highly electrophilic reactivity for the asymmetric synthesis of many organic compounds....

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Autores principales: Doraghi, Fatemeh, Aledavoud, Seyedeh Pegah, Ghanbarlou, Mehdi, Larijani, Bagher, Mahdavi, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548256/
https://www.ncbi.nlm.nih.gov/pubmed/37799175
http://dx.doi.org/10.3762/bjoc.19.106
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author Doraghi, Fatemeh
Aledavoud, Seyedeh Pegah
Ghanbarlou, Mehdi
Larijani, Bagher
Mahdavi, Mohammad
author_facet Doraghi, Fatemeh
Aledavoud, Seyedeh Pegah
Ghanbarlou, Mehdi
Larijani, Bagher
Mahdavi, Mohammad
author_sort Doraghi, Fatemeh
collection PubMed
description In the field of organosulfur chemistry, sulfenylating agents are an important key in C–S bond formation strategies. Among various organosulfur precursors, N-sulfenylsuccinimide/phthalimide derivatives have shown highly electrophilic reactivity for the asymmetric synthesis of many organic compounds. Hence, in this review article, we focus on the application of these alternative sulfenylating reagents in organic transformations.
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spelling pubmed-105482562023-10-05 N-Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations Doraghi, Fatemeh Aledavoud, Seyedeh Pegah Ghanbarlou, Mehdi Larijani, Bagher Mahdavi, Mohammad Beilstein J Org Chem Review In the field of organosulfur chemistry, sulfenylating agents are an important key in C–S bond formation strategies. Among various organosulfur precursors, N-sulfenylsuccinimide/phthalimide derivatives have shown highly electrophilic reactivity for the asymmetric synthesis of many organic compounds. Hence, in this review article, we focus on the application of these alternative sulfenylating reagents in organic transformations. Beilstein-Institut 2023-09-27 /pmc/articles/PMC10548256/ /pubmed/37799175 http://dx.doi.org/10.3762/bjoc.19.106 Text en Copyright © 2023, Doraghi et al. https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material.
spellingShingle Review
Doraghi, Fatemeh
Aledavoud, Seyedeh Pegah
Ghanbarlou, Mehdi
Larijani, Bagher
Mahdavi, Mohammad
N-Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations
title N-Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations
title_full N-Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations
title_fullStr N-Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations
title_full_unstemmed N-Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations
title_short N-Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations
title_sort n-sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548256/
https://www.ncbi.nlm.nih.gov/pubmed/37799175
http://dx.doi.org/10.3762/bjoc.19.106
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