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Authors :
Vu, Lan Phuong
Gütschow, Michael
Source :
Chemistry of Heterocyclic Compounds. Jul2020, p1-7.
Publication Year :
2020

Abstract

<break></break>4<italic>H</italic>-3,1-Benzothiazin-4-ones are accessible by various preparative routes mostly starting from anthranilic acid derivatives. These facile synthetic entries allow for the introduction of diverse substituents at positions 2 and 5–8. In this review, representative methods to generate 4<italic>H</italic>-3,1-benzothiazin-4-ones and the biological activities of the resulting products are highlighted.<break></break><break></break>4<italic>H</italic>-3,1-Benzothiazin-4-ones are accessible by various preparative routes mostly starting from anthranilic acid derivatives. These facile synthetic entries allow for the introduction of diverse substituents at positions 2 and 5–8. In this review, representative methods to generate 4<italic>H</italic>-3,1-benzothiazin-4-ones and the biological activities of the resulting products are highlighted.<break></break><break></break>4<italic>H</italic>-3,1-Benzothiazin-4-ones are accessible by various preparative routes mostly starting from anthranilic acid derivatives. These facile synthetic entries allow for the introduction of diverse substituents at positions 2 and 5–8. In this review, representative methods to generate 4<italic>H</italic>-3,1-benzothiazin-4-ones and the biological activities of the resulting products are highlighted.<break></break><break></break>4<italic>H</italic>-3,1-Benzothiazin-4-ones are accessible by various preparative routes mostly starting from anthranilic acid derivatives. These facile synthetic entries allow for the introduction of diverse substituents at positions 2 and 5–8. In this review, representative methods to generate 4<italic>H</italic>-3,1-benzothiazin-4-ones and the biological activities of the resulting products are highlighted.<break></break><break></break>4<italic>H</italic>-3,1-Benzothiazin-4-ones are accessible by various preparative routes mostly starting from anthranilic acid derivatives. These facile synthetic entries allow for the introduction of diverse substituents at positions 2 and 5–8. In this review, representative methods to generate 4<italic>H</italic>-3,1-benzothiazin-4-ones and the biological activities of the resulting products are highlighted.<break></break> [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00093122
Database :
Academic Search Index
Journal :
Chemistry of Heterocyclic Compounds
Publication Type :
Academic Journal
Accession number :
144605592
Full Text :
https://doi.org/10.1007/s10593-020-02719-z