Synthesis of indole-containing diheteroarylethenes. New probes for photochromic FRET (pcFRET)
This paper reports a synthesis of novel diheteroarylethenes functionalized for coupling to biomolecules starting from indole derivatives. The strategy is based on the derivatization at the N-atom in the indole substructure. TBDMS protection proved to be superior over BOC protection schemes, leading...
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Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_14246376_v2005_n12_p268_Giordano http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14246376_v2005_n12_p268_Giordano_oai |
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I28-R145-paper_14246376_v2005_n12_p268_Giordano_oai2020-10-19 Giordano, L. Vermeij, R.J. Jares-Erijman, E.A. 2006 This paper reports a synthesis of novel diheteroarylethenes functionalized for coupling to biomolecules starting from indole derivatives. The strategy is based on the derivatization at the N-atom in the indole substructure. TBDMS protection proved to be superior over BOC protection schemes, leading to higher yields in the overall synthesis. The suitability of the new derivatives as acceptors for pcFRET was calculated for selected donors. Fil:Giordano, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Jares-Erijman, E.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. application/pdf http://hdl.handle.net/20.500.12110/paper_14246376_v2005_n12_p268_Giordano info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar Arkivoc 2006;2005(12):268-281 Diheteroarylethenes FRET Indole derivatives Photochromism Synthesis Synthesis of indole-containing diheteroarylethenes. New probes for photochromic FRET (pcFRET) info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14246376_v2005_n12_p268_Giordano_oai |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-145 |
collection |
Repositorio Digital de la Universidad de Buenos Aires (UBA) |
topic |
Diheteroarylethenes FRET Indole derivatives Photochromism Synthesis |
spellingShingle |
Diheteroarylethenes FRET Indole derivatives Photochromism Synthesis Giordano, L. Vermeij, R.J. Jares-Erijman, E.A. Synthesis of indole-containing diheteroarylethenes. New probes for photochromic FRET (pcFRET) |
topic_facet |
Diheteroarylethenes FRET Indole derivatives Photochromism Synthesis |
description |
This paper reports a synthesis of novel diheteroarylethenes functionalized for coupling to biomolecules starting from indole derivatives. The strategy is based on the derivatization at the N-atom in the indole substructure. TBDMS protection proved to be superior over BOC protection schemes, leading to higher yields in the overall synthesis. The suitability of the new derivatives as acceptors for pcFRET was calculated for selected donors. |
format |
Artículo Artículo publishedVersion |
author |
Giordano, L. Vermeij, R.J. Jares-Erijman, E.A. |
author_facet |
Giordano, L. Vermeij, R.J. Jares-Erijman, E.A. |
author_sort |
Giordano, L. |
title |
Synthesis of indole-containing diheteroarylethenes. New probes for photochromic FRET (pcFRET) |
title_short |
Synthesis of indole-containing diheteroarylethenes. New probes for photochromic FRET (pcFRET) |
title_full |
Synthesis of indole-containing diheteroarylethenes. New probes for photochromic FRET (pcFRET) |
title_fullStr |
Synthesis of indole-containing diheteroarylethenes. New probes for photochromic FRET (pcFRET) |
title_full_unstemmed |
Synthesis of indole-containing diheteroarylethenes. New probes for photochromic FRET (pcFRET) |
title_sort |
synthesis of indole-containing diheteroarylethenes. new probes for photochromic fret (pcfret) |
publishDate |
2006 |
url |
http://hdl.handle.net/20.500.12110/paper_14246376_v2005_n12_p268_Giordano http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14246376_v2005_n12_p268_Giordano_oai |
work_keys_str_mv |
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_version_ |
1766026768838295552 |