Cargando…
A mild synthesis of N-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones()
Bromomaleimides are useful building blocks in synthesis and powerful reagents for the selective chemical modification of proteins. A mild new synthesis of these reagents is described, along with the convenient transferability of the approach to dithiomaleimides and bromopyridazinediones.
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776223/ https://www.ncbi.nlm.nih.gov/pubmed/24058217 http://dx.doi.org/10.1016/j.tetlet.2013.04.088 |
_version_ | 1782477454029357056 |
---|---|
author | Castañeda, Lourdes Wright, Zoë V.F. Marculescu, Cristina Tran, Trang M. Chudasama, Vijay Maruani, Antoine Hull, Elizabeth A. Nunes, João P.M. Fitzmaurice, Richard J. Smith, Mark E.B. Jones, Lyn H. Caddick, Stephen Baker, James R. |
author_facet | Castañeda, Lourdes Wright, Zoë V.F. Marculescu, Cristina Tran, Trang M. Chudasama, Vijay Maruani, Antoine Hull, Elizabeth A. Nunes, João P.M. Fitzmaurice, Richard J. Smith, Mark E.B. Jones, Lyn H. Caddick, Stephen Baker, James R. |
author_sort | Castañeda, Lourdes |
collection | PubMed |
description | Bromomaleimides are useful building blocks in synthesis and powerful reagents for the selective chemical modification of proteins. A mild new synthesis of these reagents is described, along with the convenient transferability of the approach to dithiomaleimides and bromopyridazinediones. |
format | Online Article Text |
id | pubmed-3776223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-37762232013-09-18 A mild synthesis of N-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones() Castañeda, Lourdes Wright, Zoë V.F. Marculescu, Cristina Tran, Trang M. Chudasama, Vijay Maruani, Antoine Hull, Elizabeth A. Nunes, João P.M. Fitzmaurice, Richard J. Smith, Mark E.B. Jones, Lyn H. Caddick, Stephen Baker, James R. Tetrahedron Lett Article Bromomaleimides are useful building blocks in synthesis and powerful reagents for the selective chemical modification of proteins. A mild new synthesis of these reagents is described, along with the convenient transferability of the approach to dithiomaleimides and bromopyridazinediones. Elsevier 2013-07-03 /pmc/articles/PMC3776223/ /pubmed/24058217 http://dx.doi.org/10.1016/j.tetlet.2013.04.088 Text en © 2013 The Authors https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license |
spellingShingle | Article Castañeda, Lourdes Wright, Zoë V.F. Marculescu, Cristina Tran, Trang M. Chudasama, Vijay Maruani, Antoine Hull, Elizabeth A. Nunes, João P.M. Fitzmaurice, Richard J. Smith, Mark E.B. Jones, Lyn H. Caddick, Stephen Baker, James R. A mild synthesis of N-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones() |
title | A mild synthesis of N-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones() |
title_full | A mild synthesis of N-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones() |
title_fullStr | A mild synthesis of N-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones() |
title_full_unstemmed | A mild synthesis of N-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones() |
title_short | A mild synthesis of N-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones() |
title_sort | mild synthesis of n-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776223/ https://www.ncbi.nlm.nih.gov/pubmed/24058217 http://dx.doi.org/10.1016/j.tetlet.2013.04.088 |
work_keys_str_mv | AT castanedalourdes amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT wrightzoevf amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT marculescucristina amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT trantrangm amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT chudasamavijay amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT maruaniantoine amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT hullelizabetha amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT nunesjoaopm amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT fitzmauricerichardj amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT smithmarkeb amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT joneslynh amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT caddickstephen amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT bakerjamesr amildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT castanedalourdes mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT wrightzoevf mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT marculescucristina mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT trantrangm mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT chudasamavijay mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT maruaniantoine mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT hullelizabetha mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT nunesjoaopm mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT fitzmauricerichardj mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT smithmarkeb mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT joneslynh mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT caddickstephen mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones AT bakerjamesr mildsynthesisofnfunctionalisedbromomaleimidesthiomaleimidesandbromopyridazinediones |