Synthesis of 6-deoxy-N-Cbz-d,l-iminoglycal-derived vinyl epoxides and examination of their regio- and stereoselectivity in nucleophilic addition reactions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
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5. Synthesis of diastereoisomeric 6-deoxy-d-allal- and 6-deoxy-d-galactal-derived allyl epoxides and examination of the regio- and stereoselectivity in nucleophilic addition reactions. Comparison with the corresponding 6-O-functionalized allyl epoxides
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1. A Mini-Review: Achievements in the Thiolysis of Epoxides;Mini-Reviews in Organic Chemistry;2020-05-31
2. Stereoselective Synthesis of Iminosugar 2-Deoxy(thio)glycosides from Bicyclic Iminoglycal Carbamates Promoted by Cerium(IV) Ammonium Nitrate and Cooperative Brønsted Acid-Type Organocatalysis;The Journal of Organic Chemistry;2020-03-11
3. Stereoselective Synthesis of Pyrans from Epoxyalkenes: Dual Catalysis with Palladium and Brønsted Acid;The Journal of Organic Chemistry;2018-05-17
4. Carba- d , l -allal- and - d , l -galactal-derived vinyl N -nosyl aziridines as useful tools for the synthesis of 4-deoxy-4-( N -nosylamino)-2,3-unsaturated-5 a -carbasugars;Tetrahedron;2017-11
5. Nucleophilic Aliphatic Substitution;Organic Reaction Mechanisms · 2013;2016-10-07
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