Synthesis of New Ferrocenyl‐Substituted Aziridines via the Gabriel–Cromwell Reaction
Author:
Affiliation:
1. a Department of Chemistry , Middle East Technical University , Ankara, Turkey
2. b Department of Chemistry , Kırıkkale University , Kırıkkale, Turkey
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1081/SCC-200054207
Reference36 articles.
1. Stereocontrolled 1,3-dipolar cycloadditions using Oppolzer's camphor sultam as the chiral auxiliary for carbonyl stabilized azomethine ylides
2. Synthesis of ferrocenyl-oxazolines by ring expansion of N-ferrocenoyl-aziridine-2-carboxylic esters
3. Asymmetric Synthesis of 2H-Azirines: First Enantioselective Synthesis of the Cytotoxic Antibiotic (R)-(-)-Dysidazirine
4. Novel Entry to a 3,4-Disubstituted 2-Azetidinone Derivative via Palladium-Assisted Carbonylation of a 2-Substituted 3-Vinylaziridine
5. Enantioselective total synthesis of (−)-indolizidines 209B and 209D via a highly efficient aza-[2,3]-wittig rearrangement of vinylaziridines
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2. Gabriel-Cromwell aziridination of amino sugars; chiral ferrocenoyl-aziridinyl sugar synthesis and their biological evaluation;Carbohydrate Research;2021-11
3. N-Ferrocenylsulfonyl-2-methylaziridine: the first ferrocene monomer for the anionic (co)polymerization of aziridines;Polymer Chemistry;2016
4. New Zinc(II)-Based Catalyst for Asymmetric Azomethine Ylide Cycloaddition Reactions;Organic Letters;2006-09-09
5. Synthesis of New Ferrocenyl-Substituted Aziridines via the Gabriel—Cromwell Reaction.;ChemInform;2005-09-06
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