Cargando…
Synthesis and kinetics of disassembly for silyl-containing ethoxycarbonyls using fluoride ions
In this study, a series of silyl-containing ethoxycarbonates and ethoxycarbamates on electron poor anilines and phenols were synthesized and their kinetics of disassembly determined in real-time upon exposure to fluoride ion sources at room temperature. The results provide a greater understanding of...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9077272/ https://www.ncbi.nlm.nih.gov/pubmed/35542569 http://dx.doi.org/10.1039/c7ra07876e |
_version_ | 1784702084772265984 |
---|---|
author | Camerino, Eugene Daniels, Grant C. Wynne, James H. Iezzi, Erick B. |
author_facet | Camerino, Eugene Daniels, Grant C. Wynne, James H. Iezzi, Erick B. |
author_sort | Camerino, Eugene |
collection | PubMed |
description | In this study, a series of silyl-containing ethoxycarbonates and ethoxycarbamates on electron poor anilines and phenols were synthesized and their kinetics of disassembly determined in real-time upon exposure to fluoride ion sources at room temperature. The results provide a greater understanding of stability and kinetics for silyl-containing protecting groups that eliminate volatile molecules upon removal, which will allow for simplification of orthogonal protection in complex organic molecules. |
format | Online Article Text |
id | pubmed-9077272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90772722022-05-09 Synthesis and kinetics of disassembly for silyl-containing ethoxycarbonyls using fluoride ions Camerino, Eugene Daniels, Grant C. Wynne, James H. Iezzi, Erick B. RSC Adv Chemistry In this study, a series of silyl-containing ethoxycarbonates and ethoxycarbamates on electron poor anilines and phenols were synthesized and their kinetics of disassembly determined in real-time upon exposure to fluoride ion sources at room temperature. The results provide a greater understanding of stability and kinetics for silyl-containing protecting groups that eliminate volatile molecules upon removal, which will allow for simplification of orthogonal protection in complex organic molecules. The Royal Society of Chemistry 2018-01-09 /pmc/articles/PMC9077272/ /pubmed/35542569 http://dx.doi.org/10.1039/c7ra07876e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Camerino, Eugene Daniels, Grant C. Wynne, James H. Iezzi, Erick B. Synthesis and kinetics of disassembly for silyl-containing ethoxycarbonyls using fluoride ions |
title | Synthesis and kinetics of disassembly for silyl-containing ethoxycarbonyls using fluoride ions |
title_full | Synthesis and kinetics of disassembly for silyl-containing ethoxycarbonyls using fluoride ions |
title_fullStr | Synthesis and kinetics of disassembly for silyl-containing ethoxycarbonyls using fluoride ions |
title_full_unstemmed | Synthesis and kinetics of disassembly for silyl-containing ethoxycarbonyls using fluoride ions |
title_short | Synthesis and kinetics of disassembly for silyl-containing ethoxycarbonyls using fluoride ions |
title_sort | synthesis and kinetics of disassembly for silyl-containing ethoxycarbonyls using fluoride ions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9077272/ https://www.ncbi.nlm.nih.gov/pubmed/35542569 http://dx.doi.org/10.1039/c7ra07876e |
work_keys_str_mv | AT camerinoeugene synthesisandkineticsofdisassemblyforsilylcontainingethoxycarbonylsusingfluorideions AT danielsgrantc synthesisandkineticsofdisassemblyforsilylcontainingethoxycarbonylsusingfluorideions AT wynnejamesh synthesisandkineticsofdisassemblyforsilylcontainingethoxycarbonylsusingfluorideions AT iezzierickb synthesisandkineticsofdisassemblyforsilylcontainingethoxycarbonylsusingfluorideions |