96791-64-9Relevant academic research and scientific papers
Diastereofacial Selectivity Studies on 3-Alkenyl-4,5-diphenyl-4,5-dihydroisoxazoles
Wade, Peter A.,Bereznak, James F.,Palfey, Bruce A.,Carroll, Patrick J.,Dailey, William P.,Sivasubramanian, S.
, p. 3045 - 3051 (2007/10/02)
Epoxidation of 3-(1-phenylethenyl)-4,5-diphenyl-4,5-dihydroisoxazole and 3-ethenyl-4,5-diphenyl-4,5-dihydroisoxazole occurred with 74percent diastereomer excess (de) and 66percent de, respectively.Catalytic cis-hydroxylation of the 3-(1-phenylethenyl)dihydroisoxazole afforded a diol with 80percent de.Cycloaddition reactions of the same alkenyl dihydroisoxazoles with bromonitrile oxide and phenylsulfonylcarbonitrile oxide occurred with 10-46percent de; opposite diastereomers were preferred in the reactions of 3-ethenyl- and 3-(1-phenylethenyl)dihydroisoxazoles.These results are rationalized based on a combination of two factors: a preference for the s-trans heterodiene conformer and a preference for attack anti to the C-4 phenyl group in all but one case.The s-trans conformer of 3-ethenyl-4,5-dihydroisoxazole was determined by the ab initio method to be 2.8 kcal/mol more stable than the s-cis conformer.
Opposite High Diastereoselectivity in the Carbonyl Addition of Organolithium and Grignard Reagents to 3-Acylisoxazolines
Wade, Peter A.,Price, David T.,McCauley, John P.,Carroll, Patrick J.
, p. 2804 - 2805 (2007/10/02)
The reactions of organolithium and Grignard reagents with 3-acyl-4,5-disubstituted-isoxazolines to produce tertiary alcohols show high but opposite diastereoselectivity; competitive pathways involving attack on s-trans and metal-chelated s-cis conformations of the O=CC=N system are proposed.
