@article{MTMT:1013242,
	title = {Synthesis and structure of cycloalkane- and norbornane-condensed 6-aryl-1,2,4,5-tetrahydropyridazinones},
	url = {https://m2.mtmt.hu/api/publication/1013242},
	author = {Csende, F and Hetényi, Anasztázia and Stájer, Géza and Fülöp, Ferenc},
	doi = {10.1002/jhet.5570410217},
	journal-iso = {J HETEROCYCLIC CHEM},
	journal = {JOURNAL OF HETEROCYCLIC CHEMISTRY},
	volume = {41},
	unique-id = {1013242},
	issn = {0022-152X},
	abstract = {The Cdouble bondN double bond of certain cis- or trans-cycloalkane and
		diexo- or diendo-norbornane-condensed pyridazinones was reduced with
		NaBH3CN. The cis- or trans nature of the starting cycloalkane
		derivatives was always retained in the saturated products, with a high
		degree of diastereoselectivity: the hydrogen on the new stereocenter
		and the annelational hydrogen next to the carbonyl always exhibited the
		same steric orientation. The stereostructures were determined by means
		of nmr measurements and confirmed by molecular modelling.},
	year = {2004},
	eissn = {1943-5193},
	pages = {259-261},
	orcid-numbers = {Hetényi, Anasztázia/0000-0001-8080-6992; Fülöp, Ferenc/0000-0003-1066-5287}
}