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- W2002567553 abstract "Highly face-selective Michael addition of lithiated Schöllkopf's bislactim ether (derived from cyclo-[L-val-glyl] 7) to E-alkenylphosphonates 2a-d and 1,3-butadienylphosphonate 2e allows a direct and stereocontrolled access to the excitatory amino acid analogues 2,3-anti-2-amino-3-substituted-4-phosphonobutanoic acids 14a-d and 2-amino-6-phosphono-4-hexenoic acid 15. The relative stereochemistry was assigned from a NMR study of cyclic derivatives 16, 17 and 19." @default.
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- W2002567553 title "Conjugate additions of E-alkenylphosphonates to lithiated Schöllkopf's bislactim ether: Stereocontrolled access to anti 2-amino-3-substituted-4-phosphonobutanoic acids" @default.
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