Wiley
Chemistry - A European Journal
,  volume 30 ,  issue 9

Annulation of a Methylenecyclopropane with Cyanoalkenes Catalyzed by Lewis Bases

Publication type: Journal Article
Publication date: 2023-12-22
Wiley
scimago Q1
wos Q2
SJR: 0.981
CiteScore: 6.7
Impact factor: 3.7
ISSN: 09476539, 15213765
General Chemistry
Catalysis
Organic Chemistry
Abstract

The annulation of a methylenecyclopropane with acyl cyanoalkenes by using DABCO or quinuclidine as a catalyst to give 2,3‐dihydofurans has been developed. A stoichiometric amount of the Lewis bases promoted the isomerization of 2,3‐dihydrofurans to furans. 1H NMR spectra of the reaction in situ revealed that the methylenecyclopropane is opened by the Lewis base to form a reaction intermediate that is added to the cyanoalkenes.

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SUZUKI I. et al. Annulation of a Methylenecyclopropane with Cyanoalkenes Catalyzed by Lewis Bases // Chemistry - A European Journal. 2023. Vol. 30. No. 9.
GOST all authors (up to 50) Copy
SUZUKI I., Kasahara N., OGURA K., Shibata I. Annulation of a Methylenecyclopropane with Cyanoalkenes Catalyzed by Lewis Bases // Chemistry - A European Journal. 2023. Vol. 30. No. 9.
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RIS Copy
TY - JOUR
DO - 10.1002/chem.202302365
UR - https://doi.org/10.1002/chem.202302365
TI - Annulation of a Methylenecyclopropane with Cyanoalkenes Catalyzed by Lewis Bases
T2 - Chemistry - A European Journal
AU - SUZUKI, Itaru
AU - Kasahara, Nozomi
AU - OGURA, Kazuki
AU - Shibata, Ikuya
PY - 2023
DA - 2023/12/22
PB - Wiley
IS - 9
VL - 30
PMID - 37798939
SN - 0947-6539
SN - 1521-3765
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2023_SUZUKI,
author = {Itaru SUZUKI and Nozomi Kasahara and Kazuki OGURA and Ikuya Shibata},
title = {Annulation of a Methylenecyclopropane with Cyanoalkenes Catalyzed by Lewis Bases},
journal = {Chemistry - A European Journal},
year = {2023},
volume = {30},
publisher = {Wiley},
month = {dec},
url = {https://doi.org/10.1002/chem.202302365},
number = {9},
doi = {10.1002/chem.202302365}
}