Taming of the DIBAL Promoted Debenzylation of α‐Cyclodextrin. Kinetics, Substituent Effects and Efficient Synthesis of Lings Tetrol**
Author:
Affiliation:
1. Department of chemistry University of Copenhagen Universitetsparken 5 2100 Copenhagen Denmark
Publisher
Wiley
Subject
General Chemistry,Catalysis,Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202200564
Reference25 articles.
1. Diisobutylaluminum-Promoted Regioselective De-O-benzylation of Perbenzylated Cyclodextrins: A Powerful New Strategy for the Preparation of Selectively Modified Cyclodextrins
2. Diisobutylaluminum-Promoted Regioselective De-O-benzylation of Perbenzylated Cyclodextrins: A Powerful New Strategy for the Preparation of Selectively Modified Cyclodextrins
3. Triisobutylaluminium and Diisobutylaluminium Hydride as Molecular Scalpels: The Regioselective Stripping of Perbenzylated Sugars and Cyclodextrins
4. Multiple Homo- and Hetero-functionalizations of α-Cyclodextrin through Oriented Deprotections
5. Supramolecular Oxidation of Anilines Using Hydrogen Peroxide as Stoichiometric Oxidant
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1. Facile Fabrication of Dual‐Activatable Gastrointestinal‐Based Nanocarriers for Safe Delivery and Controlled Release of Methotrexate;ChemPlusChem;2023-10-06
2. One-step synthesis of Ling's tetrol and its conversion into A,D-di-allo-α-cyclodextrin derivatives;Organic & Biomolecular Chemistry;2023
3. A study of the DIBAL-promoted selective debenzylation of α-cyclodextrin protected with two different benzyl groups;Beilstein Journal of Organic Chemistry;2022-11-17
4. Taming of the DIBAL Promoted Debenzylation of α‐Cyclodextrin. Kinetics, Substituent Effects and Efficient Synthesis of Lings Tetrol**;Chemistry – A European Journal;2022-04-05
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