Nucleophilic Addition onto Methyl-4H-1,4-oxazine-3-carboxylate Moiety: Short Access to 1,4-Diazine Privileged Substructures-Reference-Cited by-同舟云学术

Nucleophilic Addition onto Methyl-4H-1,4-oxazine-3-carboxylate Moiety: Short Access to 1,4-Diazine Privileged Substructures

Published:2009-03-11 Issue:7 Volume:74 Page:2911-2914
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Claveau Elise¹,Gillaizeau Isabelle¹,Kalinowska-Tluscik Justyna¹,Bouyssou Pascal¹,Coudert Gérard¹

Affiliation:

1. ICOA, UMR CNRS 6005, Université d’Orléans, 45067 Orléans Cedex 2, France, and Faculty of Chemistry, Jagiellonian University, ul. R. Ingardena 3, 30-060 Krakow, Poland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo900291f

Reference36 articles.

1. Synthesis and Reactivity of Imide-Derived Bisvinyl Phosphates. Reactivity of 2,6-Disubstituted 1,4-Dihydropyridines

2. Reactivity of bis-vinylphosphates obtained from imide derivatives. Synthesis of 2,6-disubstituted 1,4-dihydropyridines

3. Easy Access to New Heterocyclic Systems: 1,4-Oxazine and Substituted 1,4-Oxazines

4. New highlights in the synthesis and reactivity of 1,4-dihydropyrazine derivatives

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