Oxidative Annulation of 3-Aryl-2H -benzo[e][1,2,4]thiadiazine-1,1-dioxides with Aryl Aldehydes: An Easy Access to Hydroxyisoindolo[1,2-b ] benzothiadiazinedioxide Scaffolds-Reference-Cited by-同舟云学术

Oxidative Annulation of 3-Aryl-2H -benzo[e][1,2,4]thiadiazine-1,1-dioxides with Aryl Aldehydes: An Easy Access to Hydroxyisoindolo[1,2-b ] benzothiadiazinedioxide Scaffolds

Published:2020-02-13 Issue:8 Volume:2020 Page:923-931
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Kumar G. Ravi¹,Banik Swarnayu¹,Ramesh Boora¹,Sridhar Balasubramanian²,Venkata Subba Reddy Basireddy¹^ORCID

Affiliation:

1. Fluoro & Agrochemicals; CSIR-Indian Institute of Chemical Technology; 500 007 Hyderabad India

2. Laboratory of X-ray Crystallography; CSIR-Indian Institute of Chemical Technology; 500 007 Hyderabad India

Funder

Council of Scientific and Industrial Research, India

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201901509/fullpdf

Reference71 articles.

1. Synthesis and pharmacological activity of N-(2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-4-yl)-4H-1,2,4-benzothiadiazine-3-carboxamides 1,1-dioxides on rat uterus, rat aorta and rat pancreatic β-cells

2. Hydroxylated Analogues of ATP-Sensitive Potassium Channel Openers Belonging to the Group of 6- and/or 7-Substituted 3-Isopropylamino-4H-1,2,4-benzothiadiazine 1,1-Dioxides: Toward an Improvement in Sulfonylurea Receptor 1 Selectivity and Metabolism Stability

3. New Fluorinated 1,2,4-Benzothiadiazine 1,1-Dioxides: Discovery of an Orally Active Cognitive Enhancer Acting through Potentiation of the 2-Amino-3-(3-hydroxy-5-methylisoxazol-4-yl)propionic Acid Receptors

4. Chloro-Substituted 3-Alkylamino-4H-1,2,4-benzothiadiazine 1,1-Dioxides as ATP-Sensitive Potassium Channel Activators: Impact of the Position of the Chlorine Atom on the Aromatic Ring on Activity and Tissue Selectivity

5. 1,2,4-Benzothiadiazine derivatives as α1 and 5-HT1A receptor ligands

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