MOLYBDENUM HEXACARBONYL PROMOTED RING-OPENING OF HYDROXYIMINO ISOXAZOLES - UNEXPECTED PYRAZOLE FORMATION

Citation
J. Andersonmckay et al., MOLYBDENUM HEXACARBONYL PROMOTED RING-OPENING OF HYDROXYIMINO ISOXAZOLES - UNEXPECTED PYRAZOLE FORMATION, Australian Journal of Chemistry, 49(1), 1996, pp. 163-166
Citations number
26
Categorie Soggetti
Chemistry
ISSN journal
00049425
Volume
49
Issue
1
Year of publication
1996
Pages
163 - 166
Database
ISI
SICI code
0004-9425(1996)49:1<163:MHPROH>2.0.ZU;2-S
Abstract
Fused isoxazoles underwent reductive ring-opening in the presence of m olybdenum hexacarbonyl to give the corresponding beta-disubstituted co mpounds. 6-Trimethyl-6,7-dihydro-1,2-benzisoxazol-4(5H)-one oxime unde rwent reductive ring-opening in the presence of molybdenum hexacarbony l to give 3,6,6-trimethyl-6,7-dihydro-1H-indazol-4(5H)-one. A mechanis m is proposed.