Photoinduced molecular rearrangements. The photochemistry of 1,2,4-oxadiazoles in the presence of sulphur nucleophiles. Synthesis of 1,2,4-thiadiazoles-Reference-Cited by-同舟云学术

Photoinduced molecular rearrangements. The photochemistry of 1,2,4-oxadiazoles in the presence of sulphur nucleophiles. Synthesis of 1,2,4-thiadiazoles

Published:1997-09 Issue:37 Volume:53 Page:12629-12636
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Vivona Nicolò,Buscemi Silvestre,Asta Stefano,Caronna Tullio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference38 articles.

1. Ring Transformations of Five-Membered Heterocycles

2. Photoinduced Molecular Rearrangements of O-N Bond-containing Five-membered Heterocycles. An Assay for 1,2,4- and 1,2,5-Oxadiazoles

3. Photoinduced Molecular Rearrangements. Some Investigations of the Photochemical Behavior of 3-(Acylamino)-1,2,5-Oxadiazoles (Furazans)

4. A Generalized and Efficient Synthesis of 3-Amino-, 3-(N-Alkylamino)-, 3-(N,N-Dialkylamino)-5-alkyl-1,2,4-oxadiazoles by Irradiation of 3-Alkanoylamino-4-phenyl-1,2,5-oxadiazoles (Furazans)

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