4,6-Dichloro-2-oxa-5-azabicyclo[2.2.2]oct-5-en-3-ones and their Use in the Synthesis of 1,6-Dihydro-6-oxo-2-pyridine- and 6-Oxo-2-piperidinecarboxylates-Reference-Cited by-同舟云学术

4,6-Dichloro-2-oxa-5-azabicyclo[2.2.2]oct-5-en-3-ones and their Use in the Synthesis of 1,6-Dihydro-6-oxo-2-pyridine- and 6-Oxo-2-piperidinecarboxylates

Published:1996-02 Issue:7 Volume:52 Page:2591-2602
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Dubois Kristof J.,Fannes Christine C.,Compernolle Frans,Hoornaert Georges J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Aluminum Chloride Mediated Aminolysis of Lactones: A General Method for the Preparation of ω-Hydroxyalkylamides

2. Enantiomerically pure β,γ-epoxyesters from β-hydroxylactones: synthesis of β-hydroxyesters and (-)-GABOB

3. Hard acid and soft nucleophile systems. 5. Ring-opening reaction of lactones to .omega.-alkylthio- or .omega.-arylthio carboxylic acids with aluminum halide and thiol

4. Phenyl selenide anion, a superior reagent for the SN2 cleavage of esters and lactones

5. A mild, general method for conversion of esters to amides

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