@article{MTMT:1115331,
	title = {Preparation and structure of di-exo-condensed norbornane heterocycles},
	url = {https://m2.mtmt.hu/api/publication/1115331},
	author = {Miklós, Ferenc and Hetényi, Anasztázia and Sohár, Pál and Stájer, Géza},
	doi = {10.1007/s00706-003-0161-7},
	journal-iso = {MONATSH CHEM},
	journal = {MONATSHEFTE FUR CHEMIE},
	volume = {135},
	unique-id = {1115331},
	issn = {0026-9247},
	abstract = {Cyclization of di-exo-aroylnorbornanecarboxylic acid with bidentate nucleophiles (hydrazine, o-phenylenediamine, o-aminophenol, alkylenediamines, and amino alcohols) yielded heterotri-, tetra-, and pentacycles. Their structures were established by means of NMR spectroscopy, with the application of HMQC, HMBC, DEPT, DIFFNOE, and COSY methods.},
	year = {2004},
	eissn = {1434-4475},
	pages = {839-847},
	orcid-numbers = {Hetényi, Anasztázia/0000-0001-8080-6992}
}

@article{MTMT:1012773,
	title = {Synthesis and stereostructure of saturated isoindolone-fused hetero tri-, tetra-, and pentacyclic compounds},
	url = {https://m2.mtmt.hu/api/publication/1012773},
	author = {Sohár, Pál and Csámpai, Antal and Magyarfalvi, Gábor and Szabo, A E and Stájer, Géza},
	doi = {10.1007/s00706-004-0190-x},
	journal-iso = {MONATSH CHEM},
	journal = {MONATSHEFTE FUR CHEMIE},
	volume = {135},
	unique-id = {1012773},
	issn = {0026-9247},
	year = {2004},
	eissn = {1434-4475},
	pages = {1519-1527},
	orcid-numbers = {Csámpai, Antal/0000-0003-2107-7309; Magyarfalvi, Gábor/0000-0002-1464-7249}
}