Diastereoselective Lewis acid-catalysed [4+2] cycloadditions of 3-alkyl-, 3-aryl- and 3-carboxyl-2H-azirines: a route to aziridine containing azabicyclo[4.1.0]heptanes and azatricyclo[2.2.1.0]nonanes-Reference-Cited by-同舟云学术

Diastereoselective Lewis acid-catalysed [4+2] cycloadditions of 3-alkyl-, 3-aryl- and 3-carboxyl-2H-azirines: a route to aziridine containing azabicyclo[4.1.0]heptanes and azatricyclo[2.2.1.0]nonanes

Published:2002-07 Issue:30 Volume:58 Page:5983-5987
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Ray Colin A,Risberg Erik,Somfai Peter

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Hetero Diels–Alder Methodology in Organic Chemistry;Boger,1987

2. Methyl 2H-Azirine-3-carboxylates as Dienophiles: Synthesis of Methyl 1-Azabicyclo[4.1.0]-hept-3-ene-6-carboxylates

3. Generation and Diels-Alder reactions of t-butyl 2H-azirine-3-carboxylate

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