Synthesis of Bridging Chiral p–tert ‐Butylcalix[4]arenes with One and Two Carbamoyl Bridge‐Substituents through Anionic Ortho‐Fries Rearrangement
Author:
Affiliation:
1. School of PharmacyTianjin Medical University 300070 Tianjin P. R. China
2. Chengtangzhuang Street Community Health Service Centre 300222 Tianjin P. R. China
Funder
National Natural Science Foundation of China
Natural Science Foundation of Tianjin City
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202000891
Reference48 articles.
1.
2. The First Lateral Functionalization of Calix[4]arenes by a Homologous Anionic Ortho-Fries Rearrangement
3. Bridging Chiral Calix[4]arenes: Description, Optical Resolution, and Absolute Configuration Determination
4. An Approach to Optically Pure Bridging Chiral p-tert-Butylcalix[4]arenes through a Homologous Anionic Ortho-Fries Rearrangement
5. Bridging Chiral de-tert -Butylcalix[4]arenes: Diastereomeric Crystallization-Based Optical Resolution and Determination of Absolute Configuration
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1. The Versatile and Strategic O-Carbamate Directed Metalation Group in the Synthesis of Aromatic Molecules: An Update;Chemical Reviews;2024-06-12
2. tert-Butyl nitrite as a privileged reagent for a C–H bond (sub)nitration reaction in organic synthesis;New Journal of Chemistry;2024
3. Calix[4]arene Bridge Mononitration with tert-Butyl Nitrite: Synthesis of Bridging Chiral p-tert-Butylcalix[4]arene with a Mononitro Bridge Substituent;The Journal of Organic Chemistry;2022-06-01
4. Mononitration of a Calix[4]arene Methylene Bridge: Synthesis and Preliminary Catalysis Performances of Bridging Chiral p-tert-Butylcalix[4]arenes with a Monoamino Bridge Substituent in a 1,3-Alternate Conformation;The Journal of Organic Chemistry;2021-02-12
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