Stereo- and regiochemistry in the (asymmetric) cycloaddition reaction of 5-chloro-2(1 H )-pyrazinones with cyclic and monosubstituted alkenes and with a N -acryloyl substituted chiral auxiliary-Reference-Cited by-同舟云学术

Stereo- and regiochemistry in the (asymmetric) cycloaddition reaction of 5-chloro-2(1 H )-pyrazinones with cyclic and monosubstituted alkenes and with a N -acryloyl substituted chiral auxiliary

Published:2001-04 Issue:15 Volume:57 Page:3209-3220
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Rombouts Frederik J.R,Vanraes David A.J,Wynendaele Jo,Loosen Patrick K,Luyten Ingrid,Toppet Suzanne,Compernolle Frans,Hoornaert Georges J

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. Cycloadducts of ethene with 2(1H)-pyrazinones and their conversion into 2,5-diazabicyclo[2.2.2]octane-3,6-diones.

2. Cycloadducts of ethene with 2(1H)-pyrazinones functionalisation and reduction to 2,5-diazabicyclo[2.2.2]octan-3-ones.

3. Desulfurization of epidithio-2,5-piperazinedione derivatives and their open chain analogs with triphenyl phosphine

4. Synthesis of functionalized bicyclic dioxopiperazines via intramolecular epoxide opening

5. Pyrazine chemistry. Part V. Diels-Alder reactions of some 2,5-dihydroxypyrazines

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3. ChemInform Abstract: Stereo- and Regiochemistry in the (Asymmetric) Cycloaddition Reaction of 5-Chloro-2(1H)-pyrazinones with Cyclic and Monosubstituted Alkenes and with a N-Acryloyl Substituted Chiral Auxiliary.;ChemInform;2010-05-25

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