@article{MTMT:1013250,
	title = {Transformation reactions of the Betti base analog aminonaphthols},
	url = {https://m2.mtmt.hu/api/publication/1013250},
	author = {Szatmári, István and Hetényi, Anasztázia and Lázár, László and Fülöp, Ferenc},
	doi = {10.1002/jhet.5570410310},
	journal-iso = {J HETEROCYCLIC CHEM},
	journal = {JOURNAL OF HETEROCYCLIC CHEMISTRY},
	volume = {41},
	unique-id = {1013250},
	issn = {0022-152X},
	abstract = {By means of simple or domino ring-closure reactions of 1-(alpha-aminobenzyl)-2-naphthol (Betti base: 1), 1-aminomethyl-2-naplithol (2) and 2-(alpha-aminobenzyl)-1-naphthol (reverse Berri base: 3) with phosgene, ethyl benzimidate, 2-carboxybenzaldehyde, levulinic acid, salicylaldehyde/formalin or salicylaldehyde/acetaldehyde, naphth[1,2-e][1,3]oxazine and naphth[2,1-e][1,3]oxazine derivatives were prepared. All of the nitrogen-bridged polycyclic derivatives of 1 and 3 containing a number of centers of asymmetry were formed with nearly complete diastereoselectivity. Considerable differences were observed in the ring-closing abilities of the unsubstituted and phenyl-substituted aminonaphthols 1 and 2 and of the regioisomeric compounds 1 and 3.},
	year = {2004},
	eissn = {1943-5193},
	pages = {367-373},
	orcid-numbers = {Szatmári, István/0000-0002-8571-5229; Hetényi, Anasztázia/0000-0001-8080-6992; Lázár, László/0000-0002-2135-8496; Fülöp, Ferenc/0000-0003-1066-5287}
}