Chiral oxaziridines are then used in cycloaddition reactions with various substrates, including alkenes or alkynes, to form isoxazolidines. The choice of the substrate and reaction conditions can have a significant impact on the regioselectivity and diastereoselectivity of the transformation.
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N-[(E)-(4-chlorophenyl)methylidene]-1-phenylethanamine
bis(pentamethylcyclopentadienyl)phenyloxatitanacyclobutene
1,2-Diphosphorin, 1,2,3,6-tetrahydro-4,5-dimethyl-1,2-diphenyl-, trans-
2-[N'-(2,5-dimethoxybenzylidene)-N-methylhydrazino]-[1,4]naphthoquinone
[W(η(5)-C5H5)(CO)2(η(3)-H2CC[C(C.tplbond.CPh)2]CH2P(+)Ph3)]BF4
N-benzyl-(6R,1'S,2'R,3'R,4'R)-6-(3'-O-benzyl-1',2':5',6'-di-O-isopropylidene-1',2',3',4',5'-pentahydroxy-1'-pentyl)-2,3-didehydropiperidine-4-one
1H-1,2,3-Triazole, 4,5-bis(bromomethyl)-1-phenyl-
2,4-Pentadienenitrile,5-(dimethylamino)-(9CI)
methyl 3-(benzylthio)-2-cyano-2-(cyanodiphenylmethyl)-3-(isopropylimino)propanoate
1-(2-Methoxy-4-trimethylsilanylmethyl-cyclohex-3-enyl)-ethanone
Hydrazinecarboxylic acid, [(1-methyl-1H-pyrrol-2-yl)methylene]-, phenyl ester
N-(p-Nitrobenzyl)-2-methylen-4,4-dimethyl-pyrrolidin
2-(bis(phenylseleno)methylene)-1,3-diselenole
5-(4-chlorophenyl)-4-pentynoic acid chloride
