Expeditive Access to 2-Substituted 4H-Pyrido[1,3]oxazin-4-ones via an Intramolecular O-Arylation-Reference-Cited by-同舟云学术

Expeditive Access to 2-Substituted 4H-Pyrido[1,3]oxazin-4-ones via an Intramolecular O-Arylation

Published:2013-07-05 Issue:14 Volume:15 Page:3494-3497
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Slowinski Franck¹,Ben Ayad Omar¹,Ziyaret Ozge¹,Botuha Candice¹,Le Falher Laetitia¹,Aouane Kamel¹,Thorimbert Serge¹

Affiliation:

1. Sanofi R&D, Exploratory Unit, 1 Avenue Pierre Brossolette, 91385 Chilly Mazarin Cedex, France, and UPMC Sorbonne Universités, Institut Parisien de Chimie Moléculaire, UMR CNRS 7201, 4 Place Jussieu, C. 43, 75005 Paris, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol401516e

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4. Coordination studies of a fluorescent sensor for Zn 2+ detection: characterization in solution and solid state

5. Synthesis of Some 2-Aryl-1,2,4-triazolo[1,5-c][1,3]benzoxazin-5-ones as Tools To Define the Essential Pharmacophoric Descriptors of a Benzodiazepine Receptor Ligand

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