1341905-07-4Relevant academic research and scientific papers
Rhodium-catalyzed asymmetric synthesis of β-branched esters from allylic amines
Laffoon, Summer D.,Wu, Zhao,Hull, Kami L.
supporting information, p. 7814 - 7817 (2018/07/25)
Allylic amines are converted to chiral, β-branched esters under rhodium catalysis in the presence of alcohol nucleophiles. Allylic amines with aliphatic and aromatic vinylic substituents are converted to ester products with excellent enantioselectivities in all cases. Several alcohol nucleophiles have been utilized in the reaction including 1° and 2° derivatives.
Highly diastereoselective radical cyclisations of chiral sulfinimines
Rochette, Elise M.,Lewis, William,Dossetter, Al G.,Stockman, Robert A.
, p. 9395 - 9397 (2013/10/01)
Chiral amines are formed by the highly diastereoselective intramolecular addition of alkyl and aryl radicals onto chiral mesityl sulfinimines.
