Acid liability of allylic esters: use of methallyl esters as acid-labile protecting groups for car☐ylic acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Nuclear analogs of .beta.-lactam antibiotics. 2. The total synthesis of 8-oxo-4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acids
2. Removal of Allyl groups by Formic Acid Catalyzed by (Triphenylphosphane)palladium
3. Homogeneous, palladium(0)-catalyzed exchange deprotection of allylic esters, carbonates and carbamates
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1. Borane promoted aryl transfer reaction for the synthesis of α-aryl functionalised β-hydroxy and β-keto esters;Organic & Biomolecular Chemistry;2022
2. Study of O-Allylation Using Triazine-Based Reagents;Chemical and Pharmaceutical Bulletin;2017
3. Protection for the Carboxyl Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
4. Studies on the Biodegradation of Fosfomycin: Synthesis of 13C-Labeled Intermediates, Feeding Experiments with Rhizobium huakuii PMY1, and Isolation of Labeled Amino Acids from Cell Mass by HPLC;Chemistry - A European Journal;2011-10-20
5. ChemInform Abstract: Acid Lability of Allylic Esters: Use of Methallyl Esters as Acid- Labile Protecting Groups for Carboxylic Acids.;ChemInform;2010-08-21
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