Thioacetalation and Multi-Component Thiomethylative Friedel-Crafts Arylation Using BF3SMe2
Author:
Affiliation:
1. Department of Medicinal Chemistry, Uppsala University, Uppsala, Biomedical Center, P. O. Box 574, 75123 Uppsala, Sweden
Funder
Vetenskapsr?det
Uppsala Universitet
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acsomega.2c07608
Reference83 articles.
1. Boron trifluoride etherate for regioselective rearrangement or opening of secondary aryl glycidic amides
2. Low-cost synthesis of small molecule acceptors makes polymer solar cells commercially viable
3. BF3-promoted reactions of α-amino acetals with alkynes to 2,5-disubstituted pyrroles
4. Selective 5‐Exo‐Dig versus 6‐Endo‐Dig Cyclization of Benzoimidazole Thiols with Propargyl Alcohols
5. BF3·OEt2 catalyzed chemoselective CC bond cleavage of α,β-enones: an unexpected synthesis of 3-alkylated oxindoles and spiro-indolooxiranes
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