The chiral oxaziridine serves as a source of asymmetric induction in the cycloaddition reaction. The specific stereochemistry of the oxaziridine is transferred to the newly formed isoxazolidine, resulting in enantioselectivity. This chiral induction can lead to the formation of the desired isoxazolidine with high optical purity.
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N-[(E)-(4-chlorophenyl)methylidene]-1-phenylethanamine
2-(2-chlorophenyl)but-1-en-1-one
C22H32O4Si
1-O-trityl-3-O-palmitoyl-sn-glycerol
(1S,3S)-3-Benzenesulfonyl-4-methyl-1-phenyl-pent-4-en-1-ol
(2S,3S)-2-Isopropyl-3-(4-methoxy-benzylamino)-5-trimethylsilanyl-pent-4-ynethioic acid S-tert-butyl ester
N-(2-phenylpropylidene)cyclohexanamine N-oxide
(1R,5R,8R,9S)-9,10-Dimethyl-3-methylene-1,8-diphenyl-7-oxa-10-aza-spiro[4.6]undecane-6,11-dione
N-(3-butenyl)-5-phenyl-3-phenylthio-2-trimethylsilyloxymorpholine
Cycloheptene, 1-(1-methylethyl)-
ethylphenylketene (S)-sec-butylimine
2-phenyl-3-hexanol
(2S,4S)-2-(N-Benzyl-N-methylamino)-4-<
(4S,5R)-4-[2-(4-Methoxy-benzyloxy)-ethyl]-2-phenyl-[1,3]dioxan-5-ol
1,2-O-Isopropylidene-4-O-(4-toluenesulfonyl)-D-threitol
ethyl (S,R)-N-benzyloxycarbonyl-N'-acryloyl-N'-(β-phenethyl)-α,α-diaminoacetate
(1aR,2R,7bS)-2-Ethynyl-7b-(1-hydroxy-1-methyl-ethyl)-1a,7b-dihydro-2H-1-oxa-3-aza-cyclopropa[a]naphthalene-3-carboxylic acid phenyl ester
C19H25NO5S
C18H20O3S
C24H34O5Si
C30H36O3
(2R,4R,6R)-4-(carboethoxymethyl)-2-methyl-6-phenyl-1,3-dioxane
Benzenethiol, 2-[(1R)-1-(dimethylamino)ethyl]-
10,11-dihydro-5aH,17H-5,11-cyclo-dibenzo[3,4;7,8][1,5]diazocino[2,1-b]quinazolin-17-ol
Methanesulfonic acid 4-benzyloxy-2-dimethoxymethyl-butyl ester
N-(5-O-trityl-2,3-O-isopropylidene-β-D-ribofuranosyl)nitrone
[1-(6-Methoxy-3,6-dihydro-2H-pyran-2-yl)-ethyl]-carbamic acid benzyl ester
(1S,4S,7aS)-4,7a-Dimethyl-4-phenylsulfanylmethyl-1-(tetrahydro-pyran-2-yloxy)-1,2,4,6,7,7a-hexahydro-inden-5-one
