Regio- and diastereoselectivity of the 1,3-dipolar cycloaddition of α-aryl nitrone with methacrolein. A theoretical investigation
The mechanism, regio- and diastereoselectivity of the 1,3-dipolar cycloaddition of N-iso-propyl,α-(4-trifluoromethyl)-phenyl nitrone with methacrolein yielding the isoxazolidine cycloadduct has been studied at the B3LYP/6-31G(d) level of theory.
2010 ◽
Vol 51
(19)
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pp. 2617-2621
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1988 ◽
Vol 49
(C8)
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pp. C8-101-C8-102
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1997 ◽
Vol 7
(4)
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pp. 417-436
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2014 ◽
Vol 5
(1-4)
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pp. 199-206
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