A ring-closing metathesis-mediated route to novel enantiopure conformationally restricted cyclic amino acids
- 4 April 2000
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- No. 8,p. 699-700
- https://doi.org/10.1039/b001253j
Abstract
A combination of palladium-catalysed N,O-acetal formation, ruthenium-catalysed ring-closing metathesis and N-sulfonyliminium ion-mediated C–C bond formation constitutes an efficient and versatile route to a set of enantiomerically pure 2,6-disubstituted unsaturated pipecolic acid derivatives.Keywords
This publication has 0 references indexed in Scilit: