ja9070915_si_001.cif (14.33 kB)

Enantioselective Intramolecular Michael Addition of Nitronates onto Conjugated Esters: Access to Cyclic γ-Amino Acids with up to Three Stereocenters

Name: Enantioselective Intramolecular Michael Addition of Nitronates onto Conjugated Esters: Access to Cyclic γ-Amino Acids with up to Three Stereocenters
Published: 2009-11-11T00:00:00+00:00
License: https://creativecommons.org/licenses/by-nc/4.0/
Keywords: Enantioselective Intramolecular Michael Addition, Conjugated Esters, Cyclic, StereocentersEnantioselective Intramolecular Michael Addition, Access, Nitronate, Acid, Amino

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posted on 2009-11-11, 00:00 authored by William J. Nodes, David R. Nutt, Ann M. Chippindale, Alexander J. A. Cobb

Enantioselective Intramolecular Michael Addition of Nitronates onto Conjugated Esters: Access to Cyclic γ-Amino Acids with up to Three Stereocenters

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