The consecutive [2+2] cycloaddition-ring expansion route to diastereomeric 1,4-diazepin-5-ones from imino-ketenimines. Alternative intramolecular transamidation of β-lactams-Reference-Cited by-同舟云学术

The consecutive [2+2] cycloaddition-ring expansion route to diastereomeric 1,4-diazepin-5-ones from imino-ketenimines. Alternative intramolecular transamidation of β-lactams

Published:2005-02 Issue:6 Volume:61 Page:1531-1537
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Alajarín Mateo,Vidal Angel,Tovar Fulgencio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference59 articles.

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2. DBU and DBN are Strong Nucleophiles: X-Ray Crystal Structures of Onio- and Dionio-Substituted Phosphanes

3. Superior amine catalysts for the Baylis–Hillman reaction: the use of DBU and its implications†

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