Conjugated 1,8 and 1,6 addition of bis-trimethylsilylketene acetal to activated p-quinone methides via trifluoromethanesulfonic anhydride

In this work, we studied the conjugated additions of bis-trimethylsilylacetalketene acetals (bis-TMSKA) to para-quinone methides (p-QMs), which are one of the most explored molecules for the study of conjugated additions and gained significant attention in organic chemistry due to their versatile re...

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Authors: Benitez-Puebla, Luis J.; Ballinas-Indili, Ricardo; Flores-Alamo, Marcos; Guevara-Vela, José M.; Rocha-Rinza, Tomas; Rosales-Amezcua, Saulo; Alvarez-Toledano, Cecilio
Format: Article
Publication date:2025
Country:España
Institution:Universidad Autónoma de Madrid
Repository:Biblos-e Archivo. Repositorio Institucional de la UAM
Language:English
OAI Identifier:oai:dnet:biblosearchi::daead70ec7d1d022079821bcb5277410
Online Access:https://hdl.handle.net/10486/764580
https://dx.doi.org/10.1021/acs.joc.4c02852
Access Level:Open access
Keyword:Addition reactions
para-quinone methides
bis-trimethylsilylacetalketene acetals
trifluoromethanesulfonic anhydride
Química
Física
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author Benitez-Puebla, Luis J.
author2 Ballinas-Indili, Ricardo
Flores-Alamo, Marcos
Guevara-Vela, José M.
Rocha-Rinza, Tomas
Rosales-Amezcua, Saulo
Alvarez-Toledano, Cecilio
author2_role author
author
author
author
author
author
author_browse Alvarez-Toledano, Cecilio
Ballinas-Indili, Ricardo
Benitez-Puebla, Luis J.
Flores-Alamo, Marcos
Guevara-Vela, José M.
Rocha-Rinza, Tomas
Rosales-Amezcua, Saulo
author_facet Benitez-Puebla, Luis J.
Ballinas-Indili, Ricardo
Flores-Alamo, Marcos
Guevara-Vela, José M.
Rocha-Rinza, Tomas
Rosales-Amezcua, Saulo
Alvarez-Toledano, Cecilio
author_role author
collection Biblos-e Archivo. Repositorio Institucional de la UAM
description In this work, we studied the conjugated additions of bis-trimethylsilylacetalketene acetals (bis-TMSKA) to para-quinone methides (p-QMs), which are one of the most explored molecules for the study of conjugated additions and gained significant attention in organic chemistry due to their versatile reactivity, particularly in Michael addition reactions. In this study, trifluoromethanesulfonic anhydride (Tf2O) was used as an activating agent for p-QMs, aiming to achieve 1,6-Michael addition products and the least reported 1,8-Michael addition with pyridine substituents. The reactivity of p-QMs derived from pyridine demonstrated distinct reaction pathways, leading to the formation of δ and γ lactones. The investigation also involved synthesizing a 1-indanone derived from the carboxylic acids obtained from the 1,6-addition
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instname_str Universidad Autónoma de Madrid
language eng
network_acronym_str ES
network_name_str España
oai_identifier_str oai:dnet:biblosearchi::daead70ec7d1d022079821bcb5277410
publishDate 2025
publishDateSort 2025
publisher American Chemical Society
publisherStr American Chemical Society
reponame_str Biblos-e Archivo. Repositorio Institucional de la UAM
spelling Conjugated 1,8 and 1,6 addition of bis-trimethylsilylketene acetal to activated p-quinone methides via trifluoromethanesulfonic anhydride Benitez-Puebla, Luis J. Ballinas-Indili, Ricardo Flores-Alamo, Marcos Guevara-Vela, José M. Rocha-Rinza, Tomas Rosales-Amezcua, Saulo Alvarez-Toledano, Cecilio Addition reactions para-quinone methides bis-trimethylsilylacetalketene acetals trifluoromethanesulfonic anhydride Química Física In this work, we studied the conjugated additions of bis-trimethylsilylacetalketene acetals (bis-TMSKA) to para-quinone methides (p-QMs), which are one of the most explored molecules for the study of conjugated additions and gained significant attention in organic chemistry due to their versatile reactivity, particularly in Michael addition reactions. In this study, trifluoromethanesulfonic anhydride (Tf2O) was used as an activating agent for p-QMs, aiming to achieve 1,6-Michael addition products and the least reported 1,8-Michael addition with pyridine substituents. The reactivity of p-QMs derived from pyridine demonstrated distinct reaction pathways, leading to the formation of δ and γ lactones. The investigation also involved synthesizing a 1-indanone derived from the carboxylic acids obtained from the 1,6-addition Financial support was gratefully received from PAPIIT IN213523 (C. Alvarez), Consejo Nacional de Humanidades, Ciencia y Tecnología (CONAHCyT) postdoctoral scholarship No. 481594 (L.J.B.P) American Chemical Society https://hdl.handle.net/10486/764580 https://dx.doi.org/10.1021/acs.joc.4c02852
spellingShingle Conjugated 1,8 and 1,6 addition of bis-trimethylsilylketene acetal to activated p-quinone methides via trifluoromethanesulfonic anhydride
Benitez-Puebla, Luis J.
Addition reactions
para-quinone methides
bis-trimethylsilylacetalketene acetals
trifluoromethanesulfonic anhydride
Química
Física
title Conjugated 1,8 and 1,6 addition of bis-trimethylsilylketene acetal to activated p-quinone methides via trifluoromethanesulfonic anhydride
title_full Conjugated 1,8 and 1,6 addition of bis-trimethylsilylketene acetal to activated p-quinone methides via trifluoromethanesulfonic anhydride
title_fullStr Conjugated 1,8 and 1,6 addition of bis-trimethylsilylketene acetal to activated p-quinone methides via trifluoromethanesulfonic anhydride
title_full_unstemmed Conjugated 1,8 and 1,6 addition of bis-trimethylsilylketene acetal to activated p-quinone methides via trifluoromethanesulfonic anhydride
title_short Conjugated 1,8 and 1,6 addition of bis-trimethylsilylketene acetal to activated p-quinone methides via trifluoromethanesulfonic anhydride
title_sort Conjugated 1,8 and 1,6 addition of bis-trimethylsilylketene acetal to activated p-quinone methides via trifluoromethanesulfonic anhydride
topic Addition reactions
para-quinone methides
bis-trimethylsilylacetalketene acetals
trifluoromethanesulfonic anhydride
Química
Física
topic_facet Addition reactions
para-quinone methides
bis-trimethylsilylacetalketene acetals
trifluoromethanesulfonic anhydride
Química
Física
url https://hdl.handle.net/10486/764580
https://dx.doi.org/10.1021/acs.joc.4c02852