Steric constraints against [3,3]-sigmatropic rearrangement of allylic azides. A convenient approach to β-l-4-aminopent-2-enoglyceropyranosides
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference34 articles.
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1. Reinvestigation of SnCl4 catalyzed efficient synthesis of 2,3-unsaturated glycopyranosides;Carbohydrate Research;2023-12
2. Stereocontrolled Microwave-Assisted Domino [3,3]-Sigmatropic Reactions: A Winstein–Overman Rearrangement for the Formation of Differentiated Contiguous C–N Bonds;Organic Letters;2020-03-30
3. Allylic azides: synthesis, reactivity, and the Winstein rearrangement;Organic & Biomolecular Chemistry;2019
4. Regio- and stereoselective behavior of l-arabinal-derived vinyl epoxide in nucleophilic addition reactions. Comparison with conformationally restricted d-galactal-derived analogs;Tetrahedron;2015-09
5. 13C NMR Analysis of 3,6-Dihydro-2H-pyrans: Assignment of Remote Stereochemistry Using Axial Shielding Effects;The Journal of Organic Chemistry;2014-06-10
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