Selectivity in the amination of allylic alcohols via intramolecular amidomercuration

Modeling chemical reactivity. 7. The effect of a change in rate-limiting step on the stereoselectivity of electrophilic addition to allylic alcohols and related chiral alkenes

A. Richard Chamberlin, R. L. JUN. MULHOLLAND, Scott D. Kahn et al. · Journal of the American Chemical Society · 1987 · 157 citations

Natural Sciences, Chemistry, Catalysis +10

The Reduction of Multiple Bonds by Low-Valent Transition Metal Ions. The Homogeneous Reduction of Acetylenes by Chromous Sulfate

C. E. Castro, Rockne Stephens · Journal of the American Chemical Society · 1964 · 102 citations · Full text

Natural Sciences, Chemistry, Analytical Chemistry +5

Carbamate-mediated functionalization of unsaturated alcohols. 3. Intramolecular Michael addition of O-carbamates to .alpha.,.beta.-unsaturated esters. A new diastereoselective amination in an acyclic system

Masahiro Hirama, Takeo Shigemoto, Yutaka Yamazaki et al. · Journal of the American Chemical Society · 1985 · 84 citations

Natural Sciences, Chemistry, Catalysis +7

A stereocontrolled synthesis of (−)-bestatin from an acyclic allylamine by iodocyclocarbamation

Susumu Kobayashi, Toshiyuki Isobe, Masaji Ohno · Tetrahedron Letters · 1984 · 75 citations

Natural Sciences, Chemistry, Medicinal Chemistry +11

Applications of intramolecular amidomercuration. 3. Stereoselectivity in intramolecular amidomercuration. Kinetic vs. thermodynamic control

Kenn E. Harding, Thomas H. Marman · The Journal of Organic Chemistry · 1984 · 60 citations

Pharmacy, Biochemistry, Bioisosterism +5