Tandem [4 + 2]/[4 + 2] cycloaddition of bis-furyl dienes with fumaric and maleic esters at ultra-high pressure

Employment of ultra-high pressures (15 kbar) at room temperature makes it possible to prepare 1,4:5,8-diepoxynaphthalenes annulated with other heterocycles from bisfurfuryl derivatives and fumaric/maleic esters. Such a reaction does not proceed under ordinary thermal conditions.

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Publication Details

Journal
Mendeleev Communications
Published
2025-01-01
DOI
https://doi.org/10.71267/mencom.7673
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Tandem [4 + 2]/[4 + 2] cycloaddition of bis-furyl dienes with fumaric and maleic esters at ultra-high pressure

Федор И. Зубков, Н. А. Николаев, Elizaveta A. Kvyatkovskaya, Eugeniya V. Nikitina et al.
Mendeleev Communications
Catalytic Alkyne Reactions
article

Tandem [4 + 2]/[4 + 2] cycloaddition of bis-furyl dienes with fumaric and maleic esters at ultra-high pressure

Федор И. Зубков, Н. А. Николаев, Elizaveta A. Kvyatkovskaya, Eugeniya V. Nikitina, В. В. Бражкин, Alexandra G. Kutasevich, Yana S. Novoselskaya
article en

Abstract

Employment of ultra-high pressures (15 kbar) at room temperature makes it possible to prepare 1,4:5,8-diepoxynaphthalenes annulated with other heterocycles from bisfurfuryl derivatives and fumaric/maleic esters. Such a reaction does not proceed under ordinary thermal conditions.

Mendeleev CommunicationsVol. 35(3)
Peoples' Friendship University of Russia (RU), Institute for High Pressure Physics (RU)
Russian Science Foundation
Openalex Percentile: Top 95%
Catalytic Alkyne Reactions
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Tandem [4 + 2]/[4 + 2] cycloaddition of bis-furyl dienes with fumaric and maleic esters at ultra-high pressure — Федор И. Зубков, Н. А. Николаев, et al. · Mendeleev Communications (2025) | TGRS Research Map | TGRS