@article{Prousis K.C._Tzani A._Avlonitis N._ Calogeropoulou T._Detsi A._2013, title={Reactivity of 2-methyl-4H-3,1-benzoxazin-4-ones and 2-methyl-4H-pyrido[2,3- d][1,3]oxazin-4-one under microwave irradiation conditions}, volume={50}, ISSN={0022-152X}, archiveLocation={Ινστιτούτο Χημικής Βιολογίας - Επιστημονικό έργο}, url={https://hdl.handle.net/10442/17630}, DOI={10.1002/jhet.1869}, abstractNote={The reactivity of variably substituted 2-methyl-4H-3,1-benzoxazin-4-ones and 2-methyl-4H-pyrido[2,3-d][1,3]oxazin-4-one towards carbon and oxygen nucleophiles under microwave irradiation conditions was investigated. Optimization of the reaction conditions of oxazinones with carbon nucleophiles led to the synthesis of a series of 4-hydroxy-quinolin-2-ones and 4-hydroxy-1,8-naphthyridin-2-ones in high yields, whereas reaction with a variety of alcohols proceeded smoothly to the formation of the corresponding N-acetyl-anthranilates and nicotinates.}, number={6}, journal={Journal of Heterocyclic Chemistry}, author={Prousis K.C. and Tzani A. and Avlonitis N. and Calogeropoulou T. and Detsi A.}, year={2013}, pages={1313–1321} }