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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