Formation of an imidosuccinimide by cyclisation of a sterically hindered β-cyanoester with the lithium salt of a primary amine
2000 ◽
Vol 2000
(3)
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pp. 124-125
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The reaction of β-cyanoester 1 with a two-fold excess of the lithium salt of homoveratrylamine in THF at 0 °C to room temperature affords the imidosuccinimide 3, which undergoes derivation to the succinimide monooxime 4 by treatment with m-chloroperoxybenzoic acid.
2003 ◽
Vol 42
(31)
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pp. 3690-3693
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1999 ◽
Vol 121
(47)
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pp. 11006-11007
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2019 ◽
Vol 12
(06)
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pp. 1930006
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2008 ◽
Vol 112
(4)
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pp. 1189-1197
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