Autor:	Gary Knerr, John I. McKenna, David A. Quincy, Nicholas R. Natale
Rok vydání:	1988
Předmět:	chemistry.chemical_compound Fragmentation (mass spectrometry) Chemistry Dihydropyridine medicine General Medicine Isoxazole Photochemistry Bond cleavage medicine.drug
Zdroj:	ChemInform. 19
ISSN:	0931-7597
DOI:	10.1002/chin.198815042
Popis:	The mass spectral fragmentation of 4-isoxazolyl-1,4-dihydropyridines has been examined with the aid of linked metastable scanning. Three prominent pathways involve (i) O-N bond cleavage of the isoxazole followed by the loss of R2CN, (ii) loss of carboalkoxy from the 3- and/or 5- position of the dihydropyridine and, (iii) loss of the 4-isoxazolyl-substituent.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::a200f154b37cec457771056563196e1c https://doi.org/10.1002/chin.198815042 Zobrazit plný text záznamu Plný text