Cooperation of the Neutral and the Cationic Leaving Group Pathways in Acid-Catalyzed O-Benzylation of TriBOT
Author:
Affiliation:
1. Faculty of Pharmaceutical Sciences, Institute of Medical, Pharmaceutical, and Health Sciences, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan
Funder
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b01505
Reference17 articles.
1. A Novel Acid-Catalyzed O-Benzylating Reagent with the Smallest Unit of Imidate Structure
2. O-Benzylation of Carboxylic Acids Using 2,4,6-Tris(benzyloxy)-1,3,5-triazine (TriBOT) under Acidic or Thermal Conditions
3. A Practical Method for p-Methoxybenzylation of Hydroxy Groups Using 2,4,6-Tris(p-methoxybenzyloxy)-1,3,5-triazine (TriBOT-PM)
4. Development of acid-catalyzed fluorous benzylating reagents based on a triazinedione core
5. Development of a Triazine-Basedtert-Butylating Reagent, TriAT-tBu
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1. Development of a Purely Isolable (Dimorpholino)triazine-Based Reagent for the Epoxidation of Alkenes;Synlett;2024-06-28
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