The Synthesis of 3-Functionalized 5-chloro-6-methyl-2H-1,4-oxazin-2-ones and of pyridines from cycloaddition-elimination reactions with substituted acetylenic compounds.-Reference-Cited by-同舟云学术

The Synthesis of 3-Functionalized 5-chloro-6-methyl-2H-1,4-oxazin-2-ones and of pyridines from cycloaddition-elimination reactions with substituted acetylenic compounds.

Published:1994-04 Issue:17 Volume:50 Page:5211-5224
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Van Aken Koen J.,Lux Gerrit M.,Deroover Geert G.,Meerpoel Lieven,Hoornaert Georges J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. Über 1.4‐Oxazine, VII. Oxydation des 5.6‐Dihydro‐1.4‐oxazinon‐(2)‐Systems zu 1.4‐Oxazinonen‐(2)

2. Darstellung und Eigenschaften von 3,6‐Dihydro‐2 H ‐1,4‐oxazin‐2‐onen und 2 H ‐1,4‐Oxazin‐2‐onen

3. Chloro (ethoxycarbonyl)methyleneiminium salts - versatile electrophilic intermediates for heterocyclic synthesis

4. Synthesis of 3,5-dihalogeno-2H-1,4-oxazin-2-ones from cyanohydrines

5. A General Synthesis of 3,5-Dihalo-2H-1,4-oxazin-2-ones from Cyanohydrins

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