Synthesis of 1H- and 5H-1,3-diazepines from azido- and tetrazolo-pyridines

Reisinger, A and Wentrup, C (1996) Synthesis of 1H- and 5H-1,3-diazepines from azido- and tetrazolo-pyridines. Chemical Communications, 7: 813-814. doi:10.1039/cc9960000813


Author Reisinger, A
Wentrup, C
Title Synthesis of 1H- and 5H-1,3-diazepines from azido- and tetrazolo-pyridines
Journal name Chemical Communications   Check publisher's open access policy
ISSN 1359-7345
Publication date 1996-04-01
Year available 1996
Sub-type Article (original research)
DOI 10.1039/cc9960000813
Open Access Status Not yet assessed
Issue 7
Start page 813
End page 814
Total pages 2
Place of publication CAMBRIDGE
Publisher ROYAL SOC CHEMISTRY
Language eng
Abstract Stable 1H-1,3-diazepines 7-9, 10, 13, 14, 17 and 19 are obtained, often in high yields, by photolysis of trifluoromethyl-substituted azido- or tetrazolo-pyridines in the presence of alcohols or amines; in some cases, 5H-1,3-diazepines are also formed (11, 21 and 23).
Keyword Diazepines
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Unknown

Document type: Journal Article
Sub-type: Article (original research)
Collection: ResearcherID Downloads - Archived
 
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