78781-86-9Relevant academic research and scientific papers
Stereoselective synthesis of 2-(2'-cycloalkenyl) glycinates via [3,3] sigmatropic rearrangement of chelated ester-enolates
Kazmaier
, p. 12895 - 12902 (1994)
Ester-enolate Claisen rearrangement of chelated N-protected cycloalkenyl glycinates 1 results in the formation of cyclic γ,δ-unsaturated amino acids in good yields and in a highly diastereoselective fashion.
