A novel analogue of Asinger reaction for the synthesis of thiazinoquinoline derivatives

The unexpected synthesis of 2 H -[1,3]thiazino[6,5- b ]quinoline derivatives from domino cyclic condensation of 2-mercaptoquinoline-3-carbaldehyde and ammonium acetate at ambient temperature in EtOH was described. Graphical abstract

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Bibliographic Details
Published inMonatshefte für Chemie Vol. 148; no. 2; pp. 315 - 320
Main Authors Faghihi, Zeinab, Oskooie, Hossein Abdi, Heravi, Majid M., Tajbakhsh, Mahmoud, Shiri, Morteza
Format Journal Article
LanguageEnglish
Published Vienna Springer Vienna 01.02.2017
Springer Nature
Springer Nature B.V
Subjects
Analytical Chemistry
Chemical reactions
Chemistry
Chemistry and Materials Science
Chemistry, Multidisciplinary
Chemistry/Food Science
Inorganic Chemistry
Organic Chemistry
Original Paper
Physical Chemistry
Physical Sciences
Science & Technology
Theoretical and Computational Chemistry
Asinger reaction
Cyclization
Thiazinoquinoline
Catalyst-free
Condensation
2-Mercaptoquinoline-3-carbaldehydes
NATURAL-PRODUCTS
FRIEDLANDER QUINOLINE SYNTHESIS
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Summary:The unexpected synthesis of 2 H -[1,3]thiazino[6,5- b ]quinoline derivatives from domino cyclic condensation of 2-mercaptoquinoline-3-carbaldehyde and ammonium acetate at ambient temperature in EtOH was described. Graphical abstract
ISSN:0026-9247
1434-4475
DOI:10.1007/s00706-016-1755-1