- In
organic chemistry,
ammoxidation is a
process for the
production of
nitriles (R−C≡N)
using ammonia (NH3) and
oxygen (O2). It is
sometimes called the...
- The
Sharpless oxyamination (often
known as
Sharpless aminohydroxylation) is the
chemical reaction that
converts an
alkene to a
vicinal amino alcohol. The...
-
asymmetric dihydroxylation,
Sharpless oxyamination)
during the 1970s and 1980s. With the
asymmetric oxyamination reaction,
using osmium tetroxide, being...
- Herranz, Eugenio; Sharpless, K.
Barry (1983). "Osmium-catalyzed
Vicinal Oxyamination of
Olefins by N-chloro-N-Argentocarbamates:
Ethyl Threo-[1-(2-hydroxy-1...
- (Sharpless epoxidation,
Sharpless asymmetric dihydroxylation,
Sharpless oxyamination). The
other half of the year's
Prize was
shared between William S. Knowles...
- Herranz, Eugenio; Sharpless, K.
Barry (1983). "Osmium-catalyzed
Vicinal Oxyamination of
Olefins by N-chloro-N-Argentocarbamates:
Ethyl Threo-[1-(2-hydroxy-1...
- Osmium(VIII)
oxide is also used in
catalytic amounts in the
Sharpless oxyamination to give
vicinal amino-alcohols. In
combination with
sodium periodate...
-
Sharpless epoxidation,
Sharpless asymmetric dihydroxylation, and
Sharpless oxyamination. 1985
Harold Kroto,
Robert Curl and
Richard Smalley discover fullerenes...
-
produced in situ from
sodium hydroxide and
chlorine (Cl2): The
Sharpless oxyamination converts an
alkene to a
vicinal aminoalcohol. A
common source of the...
-
Sharpless epoxidation,
Sharpless asymmetric dihydroxylation, and
Sharpless oxyamination. In 1985,
Harold Kroto,
Robert Curl and
Richard Smalley discovered fullerenes...
