Increased formation of oxepanes in non-aqueous medium in the cycloaddition of 3-O-allyl-1,2-isopropylidenefuranose N-Ph nitrones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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3. Optically active isoxazolidines via asymmetric cycloaddition reactions of nitrones with alkenes: applications in organic synthesis
4. Synthesis of chiral oxepanes and pyrans by 3-O-allylcarbohydrate nitrone cycloaddition (3-OACNC)
5. Intramolecular 1,3-dipolar nitrone and nitrile oxide cycloaddition of 2- and 4-O-allyl and propargyl glucose derivatives: a versatile approach to chiral cyclic ether fused isoxazolidines, isoxazolines and isoxazoles
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1. 1,3-Dipolar cycloaddition reaction on carbohydrate template: Stereoselective synthesis of glycospiroheterocycles;Tetrahedron;2020-08
2. Advancements in synthetic and structural studies of septanoside sugars;Recent Trends in Carbohydrate Chemistry;2020
3. Epimerization of the α Stereocenter ind-Ribose-Derived Nitrones: Direct Access to Variant Quinolizidines withd-Ribo andd-Arabino Configurations;Asian Journal of Organic Chemistry;2015-06-12
4. Recent progress in the synthesis of oxepanes and medium ring ethers;Tetrahedron;2012-09
5. Carbohydrate nitrone and nitrile oxide cycloaddition approach to chiral sulfur heterocycles and nucleosides;RSC Advances;2012
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