Royal Society of Chemistry, Organic Chemistry Frontiers, 17(7), p. 2505-2510, 2020
DOI: 10.1039/c9qo01304k
Full text: Unavailable
Complementary asymmetric reductions of N-benzyl-α-keto amides were achieved for the first time by an air and moisture stable, reduced form of vanadyl(v) N-salicylidene-t-leucinate with HBPin and HBCat with up to 99% and 90% ee, respectively.