Peer-reviewedLicence not statedTetrahedron Letters
p-Methoxybenzyl-N-phenyl-2,2,2-trifluoroacetimidate: a versatile reagent for mild acid catalyzed etherification
Related
- FtmOx1-catalyzed diverse C(sp3)-H oxyfunctionalization enables versatile late-stage diversification of phenethylamines and tetrahydroisoquinolines
- Catalytic Performance of Post-Treated Thin-Plate ZSM-5 for Allyl Alcohol Etherification
- Visible-light-Enabled O-Selective Radical Etherification of 1,2-Dicarbonyl Compounds for the Synthesis of Sterically Congested Ethers
- Nitrous oxide as diazo transfer reagent
- Origin of Reagent-Dependent Diastereoselectivity in Grignard Additions to a TADDOL-Derived α-Ketiminophosphonate
BibTeX
@article{barrocaaubry2026pmethoxybenzylnphenyl222trifluoroacetimidate,
title = {{p-Methoxybenzyl-N-phenyl-2,2,2-trifluoroacetimidate: a versatile reagent for mild acid catalyzed etherification}},
author = {Nadine Barroca-Aubry and Mohamed Benchekroun and Filipe Gomes and David Bonnaffé},
journal = {Tetrahedron Letters},
year = {2026},
month = oct,
doi = {10.1016/j.tetlet.2013.07.066},
url = {https://hal.science/hal-05787239v1},
}
RIS
TY - JOUR
TI - p-Methoxybenzyl-N-phenyl-2,2,2-trifluoroacetimidate: a versatile reagent for mild acid catalyzed etherification
AU - Nadine Barroca-Aubry
AU - Mohamed Benchekroun
AU - Filipe Gomes
AU - David Bonnaffé
PY - 2026
DA - 2026/10/08
JO - Tetrahedron Letters
DO - 10.1016/j.tetlet.2013.07.066
UR - https://hal.science/hal-05787239v1
SN - 0040-4039
SN - 1873-3581
ER -