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- W4236634762 abstract "Playing two roles at once, chiral amines from L-proline or D-mannitol act as protecting groups and as chiral auxiliaries in the [2+2] cycloaddition of formaldehyde hydrazones, such as 1, to ketenes. This strategy, based on the stability of the hydrazones as methanimines and on the development of a new oxidative cleavage of hydrazides, provides a short entry to enantiopure 4-unsubstituted 3-alkoxy- and 3-aminoazetidinones with desired configurations. X=OBn, N(CO2Bn)Bn; Bn=benzyl; MMPP=magnesium monoperoxyphthalate." @default.
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- W4236634762 date "2000-08-18" @default.
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- W4236634762 title "Enantioselective Synthesis of 4-Unsubstituted 3-Alkoxy- and 3-Aminoazetidin-2-ones from FormaldehydeN,N-Dialkylhydrazones" @default.
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- W4236634762 doi "https://doi.org/10.1002/1521-3773(20000818)39:16<2893::aid-anie2893>3.0.co;2-e" @default.
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