Mark E. Okazaki

Synthesis applications of aza-Cope rearrangements. 11. Carbon-carbon bond formation under mild conditions via tandem cationic aza-Cope rearrangement-Mannich reactions. A convenient synthesis of polysubstituted pyrrolidines

Larry E. Overman, Masa‐aki Kakimoto, Mark E. Okazaki et al. · Journal of the American Chemical Society · 1983 · 58 citations

Engineering, Natural Sciences, Diversity-oriented Synthesis +10

-Butyldiphenylsilylamines: A useful protecting group for primary amines

Larry E. Overman, Mark E. Okazaki, Pratibha Mishra · Tetrahedron Letters · 1986 · 48 citations

Engineering, Useful Protecting Group, Organic Chemistry +2

A formal total synthesis of (.+-.)-laurenene

Leo A. Paquette, Mark E. Okazaki, Jean Claude Caille · The Journal of Organic Chemistry · 1988 · 33 citations

Altmetrics, Engineering, Donut Icon +13

Synthesis applications of cationic aza-Cope rearrangements. 16. Stereocontrolled synthesis of substituted cis-cyclopenta[b]pyrrolidines

Larry E. Overman, Mark E. Okazaki, E. Jon Jacobsen · The Journal of Organic Chemistry · 1985 · 30 citations

Cationic Aza-cope Rearrangements, Heterocyclic, Natural Sciences +10