1334472-65-9Relevant academic research and scientific papers
Highly enantioselective γ-amination of α,β-unsaturated acyl chlorides with azodicarboxylates: Efficient synthesis of chiral γ-amino acid derivatives
Shen, Li-Tao,Sun, Li-Hui,Ye, Song
supporting information; experimental part, p. 15894 - 15897 (2011/11/13)
The cinchona alkaloid-catalyzed γ-amination of α,β- unsaturated acyl chlorides with azodicarboxylates to give the corresponding dihydropyridazinones in good yields with high enantioselectivities has been developed. Reductive ring opening of the dihydropyr
