Anionic inverse electron-demand 1,3-dipolar cycloaddition of nitrones with ynolates.: Facile stereoselective synthesis of 5-isoxazolidinones leading to β-amino acids
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作者:
Shindo, M
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Univ Tokushima, Inst Med Resources, Tokushima 7708505, JapanUniv Tokushima, Inst Med Resources, Tokushima 7708505, Japan
Shindo, M
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Itoh, K
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Univ Tokushima, Inst Med Resources, Tokushima 7708505, JapanUniv Tokushima, Inst Med Resources, Tokushima 7708505, Japan
Itoh, K
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Tsuchiya, C
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Univ Tokushima, Inst Med Resources, Tokushima 7708505, JapanUniv Tokushima, Inst Med Resources, Tokushima 7708505, Japan
Tsuchiya, C
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Shishido, K
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Univ Tokushima, Inst Med Resources, Tokushima 7708505, JapanUniv Tokushima, Inst Med Resources, Tokushima 7708505, Japan
Shishido, K
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]
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[1] Univ Tokushima, Inst Med Resources, Tokushima 7708505, Japan
[GRAPHICS] The inverse electron-demand 1,3-dipolar cycloaddition of nitrones with ynolates, followed by quenching with t-BuOH, produced substituted 5-isoxazolidinones with good trans-selectivity. These products were easily converted into beta-amino acids.