Iron-Catalyzed Synthesis of α-Azido α-Amino Esters via the Alkylazidation of Alkenes
Author:
Affiliation:
1. Laboratory of Catalysis and Organic Synthesis, Institut des Sciences et Ingénierie Chimique, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland
Funder
NCCR Catalysis
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c02153
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5. Kataine Fadgyas, K.; Farkas, J.; Lukacs, G.; Lang, F.; Jurak, F.; Csala, I.; Koroknai, T.; Porcs-Makkay, M. Process for the preparation of Carbipoda. WO 2007/042848A2, 2007.
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1. Electrochemical oxidative heterodifunctionalization of dehydroalanine: access to unnatural α,α-disubstituted amino esters;Organic Chemistry Frontiers;2024
2. Iron-catalyzed group-transfer reactions with iodine(III) reagents;Advances in Catalysis;2024
3. Fe-Catalyzed Alkylazidation of Alkenes for the Synthesis of α-Azido α-Amino Esters;Synfacts;2023-11-15
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