Combining α-amidoalkylation reactions of N-acyliminium ions with ring-closing metathesis: access to versatile novel isoindolones spirocyclic compounds-Reference-Cited by-同舟云学术

Combining α-amidoalkylation reactions of N-acyliminium ions with ring-closing metathesis: access to versatile novel isoindolones spirocyclic compounds

Published:2013-09 Issue:38 Volume:54 Page:5227-5231
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Pesquet Anthony,Othman Mohamed

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference70 articles.

1. Rhodium catalyzed synthesis of isoindolinones via C–H activation of N-benzoylsulfonamides

2. Nickel(0)-Catalyzed Cyclization of N-Benzoylaminals for Isoindolinone Synthesis

3. New efficient access to fused (Het)Aryltetrahydroindolizinones via N-acyl iminium intermediates

4. Palladium-Catalyzed One-Step Synthesis of Isoindole-1,3-diones by Carbonylative Cyclization of o-Halobenzoates and Primary Amines

5. Syntheses of Substituted 3-Methyleneisoindolin-1-ones By a Palladium-Catalyzed Sonogashira Coupling−Carbonylation−Hydroamination Sequence in Phosphonium Salt-Based Ionic liquids

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