1 formation of alpha-ketoisocaproate, which is reductively aminated back to L-leucine by leucine dehydr

2 velopment of a complementary reaction, which reductively aminates the C-C sigma-bond of carbonyls, no

3      Acid hydrolysis of 6 gave 11, which was reductively aminated to give (+/-)-narwedine 2.

4 e fragmentation characteristics of N-glycans reductively aminated with 2-aminobenzoic acid and 2-amin

5     The resulting oligosaccharides were then reductively aminated with 2-aminopyridine and the struct

6 re released by treatment with N-glycanase F, reductively aminated with anthranilic acid, and fraction