Diels–Alder cycloaddition of 2-azadienes to methyl 2-(2,6-dichlorophenyl)-2H-azirine-3-carboxylate in the synthesis of methyl 4-oxo-1,3-diazabicyclo[4.1.0]heptane-6-carboxylates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Cycloaddition of methyl 2-(2,6-dichorophenyl)-2H-azirine-3-carboxylate to electron-rich 2-azadienes
2. Verbesserte Synthese von α-Azidozimtsäure-estern und 2H-Azirinen
3. Methyl 2H-Azirine-3-carboxylates as Dienophiles: Synthesis of Methyl 1-Azabicyclo[4.1.0]-hept-3-ene-6-carboxylates
4. Methyl 2-aryl-2H-azirine-3-carboxylates as dienophiles
5. Generation and Diels-Alder reactions of t-butyl 2H-azirine-3-carboxylate
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1. Non-Aziridination Approaches to 3-Arylaziridine-2-carboxylic Acid Derivatives and 3-Aryl-(aziridin-2-yl)ketones;International Journal of Molecular Sciences;2022-05-25
2. Evaluation of the mechanism, regio-, and diastereoselectivity of aza-Diels–Alder reactions of 2H-azirine under a Lewis acid catalyst;Structural Chemistry;2022-01-07
3. Acid-Catalyzed 1,3-Dipolar Cycloaddition of 2H-Azirines with Nitrones: An Unexpected Access to 1,2,4,5-Tetrasubstituted Imidazoles;The Journal of Organic Chemistry;2020-02-05
4. 1-( N -Acylamino)-1-triphenylphosphoniumalkylphosphonates: General synthesis and prospects for further synthetic applications;Tetrahedron Letters;2018-08
5. Evolution of the Aza-Diels–Alder Reaction of 2H-Azirines;Synlett;2016-06-21
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