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  Diels-Alder-Reaktion eines elektronenarmen C-Acylimins mit Tetraethoxyethylen

Felderhoff, M., & Sustmann, R. (1996). Diels-Alder-Reaktion eines elektronenarmen C-Acylimins mit Tetraethoxyethylen. Monatshefte für Chemie / Chemical Monthly, 127(8-9), 967-970. doi:10.1007/BF00807037.

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 Creators:
Felderhoff, Michael1, 2, Author           
Sustmann, R.2, Author
Affiliations:
1Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445589              
2UniversitO.t GH Essen, Institut fiir Organische Chemic, D-45117 Essen, Deutschland, ou_persistent22              

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Free keywords: C-Acylimine Diels-Alder Reaction [4+2] Cycloaddition 1,4-Oxazine
 Abstract: The synthesis of two C-acylimines and their reactivity towards electron rich dienophiles inDiels-Alder reactions is described. A [4+2] cycloadduct is obtained only in one case: from the reaction of a C-acylimine substituted by two methoxycarbonyl groups with tetraethoxyethylene. No [2+2] cycloadducts are observed.

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Language(s): deu - German
 Dates: 1996-08
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1007/BF00807037
 Degree: -

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Title: Monatshefte für Chemie / Chemical Monthly
Source Genre: Journal
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Publ. Info: Wien : Springer-Verlag Wien
Pages: - Volume / Issue: 127 (8-9) Sequence Number: - Start / End Page: 967 - 970 Identifier: ISSN: 0026-9247
CoNE: https://pure.mpg.de/cone/journals/resource/110992357314682_1