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Flow technology enabled preparation of C3-heterosubstituted 1-azabicyclo[1.1.0]butanes and azetidines: accessing unexplored chemical space in strained heterocyclic chemistry

Pantaleo Musci, Marco Colella, Michael Andresini, Andrea Aramini, Leonardo Degennaro, Renzo Luisi

2022Chemical Communications39 citationsDOI

Abstract

O-ring) were also evaluated. New chemical space has been explored and new structural motifs such as ABB-aziridines or spiro azetidine-oxazetidines are also reported.

Topics & Concepts

ChemoselectivityReactivity (psychology)Ring (chemistry)Chemical spaceChemistryAzetidineContinuous flowSpace (punctuation)StereochemistryCombinatorial chemistryComputer scienceOrganic chemistryPhysicsCatalysisDrug discoveryOperating systemPathologyMechanicsAlternative medicineBiochemistryMedicineSynthesis and Catalytic ReactionsInnovative Microfluidic and Catalytic Techniques InnovationAsymmetric Hydrogenation and Catalysis
Flow technology enabled preparation of C3-heterosubstituted 1-azabicyclo[1.1.0]butanes and azetidines: accessing unexplored chemical space in strained heterocyclic chemistry | Litcius