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Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine

Chromium-catalyzed cyclopropanation of alkenes with bromoform was achieved to produce the corresponding bromocyclopropanes. In this catalytic cyclopropanation, an organosilicon reductant, 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine (1a), was indispensable for reducing CrCl(3)(thf...

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Autores principales: Ikeda, Hideaki, Nishi, Kohei, Tsurugi, Hayato, Mashima, Kazushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152687/
https://www.ncbi.nlm.nih.gov/pubmed/34094048
http://dx.doi.org/10.1039/d0sc00964d
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author Ikeda, Hideaki
Nishi, Kohei
Tsurugi, Hayato
Mashima, Kazushi
author_facet Ikeda, Hideaki
Nishi, Kohei
Tsurugi, Hayato
Mashima, Kazushi
author_sort Ikeda, Hideaki
collection PubMed
description Chromium-catalyzed cyclopropanation of alkenes with bromoform was achieved to produce the corresponding bromocyclopropanes. In this catalytic cyclopropanation, an organosilicon reductant, 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine (1a), was indispensable for reducing CrCl(3)(thf)(3) to CrCl(2)(thf)(3), as well as for in situ generation of (bromomethylidene)chromium(iii) species from (dibromomethyl)chromium(iii) species. The (bromomethylidene)chromium(iii) species are proposed to react spontaneously with alkenes to give the corresponding bromocyclopropanes. This catalytic cyclopropanation was applied to various olefinic substrates, such as allyl ethers, allyl esters, terminal alkenes, and cyclic alkenes.
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spelling pubmed-81526872021-06-03 Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine Ikeda, Hideaki Nishi, Kohei Tsurugi, Hayato Mashima, Kazushi Chem Sci Chemistry Chromium-catalyzed cyclopropanation of alkenes with bromoform was achieved to produce the corresponding bromocyclopropanes. In this catalytic cyclopropanation, an organosilicon reductant, 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine (1a), was indispensable for reducing CrCl(3)(thf)(3) to CrCl(2)(thf)(3), as well as for in situ generation of (bromomethylidene)chromium(iii) species from (dibromomethyl)chromium(iii) species. The (bromomethylidene)chromium(iii) species are proposed to react spontaneously with alkenes to give the corresponding bromocyclopropanes. This catalytic cyclopropanation was applied to various olefinic substrates, such as allyl ethers, allyl esters, terminal alkenes, and cyclic alkenes. The Royal Society of Chemistry 2020-03-11 /pmc/articles/PMC8152687/ /pubmed/34094048 http://dx.doi.org/10.1039/d0sc00964d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Ikeda, Hideaki
Nishi, Kohei
Tsurugi, Hayato
Mashima, Kazushi
Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine
title Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine
title_full Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine
title_fullStr Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine
title_full_unstemmed Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine
title_short Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine
title_sort chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152687/
https://www.ncbi.nlm.nih.gov/pubmed/34094048
http://dx.doi.org/10.1039/d0sc00964d
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