The use of enantiomerically pure N-sulfinimines in asymmetric Baylis–Hillman reactions
- 18 February 2002
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 43 (8) , 1577-1581
- https://doi.org/10.1016/s0040-4039(02)00021-7
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- Selective Formation of α-Methylene-β-amino acid Derivatives through the Aza Version of the Baylis−Hillman ReactionThe Journal of Organic Chemistry, 2001
- Enantiomerically Pure α-Alkylidene β-Amino Esters from Asymmetric Addition of Metal Dienolates to N-SulfinyliminesThe Journal of Organic Chemistry, 1998
- Asymmetric synthesis of amino acids using sulfinimines (thiooxime S-oxides)Chemical Society Reviews, 1998
- An Efficient Synthesis of (S)-(+)-Ethyl β-Amino-3-pyridinepropanoate Using Enantiopure SulfiniminesThe Journal of Organic Chemistry, 1996
- Asymmetric Synthesis of (R)-(+)-.beta.-Phenylalanine from (S)-(+)-Benzylidene-p-toluenesulfinamide. Regeneration of the Sulfinimine PrecursorThe Journal of Organic Chemistry, 1995
- A Simple, Mild Synthesis of 3-Aryl-2-methylidene-3-(p-tolylsulfonylamino)propanoatesAustralian Journal of Chemistry, 1995
- Planar Chiral Arylaldehydeimine Tricarbonylchromium Complexes in the Asymmetric Baylis - Hillman Coupling ReactionSynlett, 1994
- Asymmetric synthesis of sulfinimines: applications to the synthesis of nonracemic .beta.-amino acids and .alpha.-hydroxyl .beta.-amino acidsThe Journal of Organic Chemistry, 1992
- A model for the diastereofacial differentiation in the alkylation of endocyclic enolateJournal of the American Chemical Society, 1988
- Diastereoselective Hydrogenation of Methyl 2-[α-(Methoxycarbonylamino)benzyl]acrylate Catalyzed by Ru(II) or Rh(I) ComplexesBulletin of the Chemical Society of Japan, 1988