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Modular Synthesis of (Borylmethyl)silanes through Orthogonal Functionalization of a Carbon Atom

[Image: see text] (Borylmethyl)trimethylsilanes are important building blocks in organic synthesis displaying a unique reactivity. Yet, the synthesis of more advanced derivatives is limited by the advanced silicon intermediates required for their preparation. Herein, a one-pot synthesis of (borylmet...

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Autores principales: Chowdhury, Rajdip, Elek, Gábor Zoltán, Meana-Baamonde, Beatriz, Mendoza, Abraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043938/
https://www.ncbi.nlm.nih.gov/pubmed/36898045
http://dx.doi.org/10.1021/acs.orglett.3c00474
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author Chowdhury, Rajdip
Elek, Gábor Zoltán
Meana-Baamonde, Beatriz
Mendoza, Abraham
author_facet Chowdhury, Rajdip
Elek, Gábor Zoltán
Meana-Baamonde, Beatriz
Mendoza, Abraham
author_sort Chowdhury, Rajdip
collection PubMed
description [Image: see text] (Borylmethyl)trimethylsilanes are important building blocks in organic synthesis displaying a unique reactivity. Yet, the synthesis of more advanced derivatives is limited by the advanced silicon intermediates required for their preparation. Herein, a one-pot synthesis of (borylmethyl)silanes is developed, sourced on available alkyl-, aryl-, alkoxy-, aryloxy-, and silyl-hydrosilane materials. The privileged reactivity of N-hydroxyphthalimidyl diazoacetate (NHPI-DA) in Si–H insertion and α-silyl redox-active esters in different decarboxylative borylation reactions are scrutinized.
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spelling pubmed-100439382023-03-29 Modular Synthesis of (Borylmethyl)silanes through Orthogonal Functionalization of a Carbon Atom Chowdhury, Rajdip Elek, Gábor Zoltán Meana-Baamonde, Beatriz Mendoza, Abraham Org Lett [Image: see text] (Borylmethyl)trimethylsilanes are important building blocks in organic synthesis displaying a unique reactivity. Yet, the synthesis of more advanced derivatives is limited by the advanced silicon intermediates required for their preparation. Herein, a one-pot synthesis of (borylmethyl)silanes is developed, sourced on available alkyl-, aryl-, alkoxy-, aryloxy-, and silyl-hydrosilane materials. The privileged reactivity of N-hydroxyphthalimidyl diazoacetate (NHPI-DA) in Si–H insertion and α-silyl redox-active esters in different decarboxylative borylation reactions are scrutinized. American Chemical Society 2023-03-10 /pmc/articles/PMC10043938/ /pubmed/36898045 http://dx.doi.org/10.1021/acs.orglett.3c00474 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Chowdhury, Rajdip
Elek, Gábor Zoltán
Meana-Baamonde, Beatriz
Mendoza, Abraham
Modular Synthesis of (Borylmethyl)silanes through Orthogonal Functionalization of a Carbon Atom
title Modular Synthesis of (Borylmethyl)silanes through Orthogonal Functionalization of a Carbon Atom
title_full Modular Synthesis of (Borylmethyl)silanes through Orthogonal Functionalization of a Carbon Atom
title_fullStr Modular Synthesis of (Borylmethyl)silanes through Orthogonal Functionalization of a Carbon Atom
title_full_unstemmed Modular Synthesis of (Borylmethyl)silanes through Orthogonal Functionalization of a Carbon Atom
title_short Modular Synthesis of (Borylmethyl)silanes through Orthogonal Functionalization of a Carbon Atom
title_sort modular synthesis of (borylmethyl)silanes through orthogonal functionalization of a carbon atom
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043938/
https://www.ncbi.nlm.nih.gov/pubmed/36898045
http://dx.doi.org/10.1021/acs.orglett.3c00474
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