- The
Sharpless oxyamination (often
known as
Sharpless aminohydroxylation) is the
chemical reaction that
converts an
alkene to a
vicinal amino alcohol. The...
- G.V.; Creswell, M.; Seely, F.; Devroy, W. (1986). "Iron-Catalyzed
Aminohydroxylation of Olefins". Organometallics. 5 (11): 2395–2398. doi:10.1021/om00142a044...
-
synthesis from
science fiction to the
relatively routine,
including aminohydroxylation, dihydroxylation, and the
Sharpless asymmetric epoxidation. In 2001...
-
catalytic oxidation Milas hydroxylation Upjohn dihydroxylation Sharpless aminohydroxylation Lemieux–Johnson
oxidation -
olefin to diol,
followed by oxidative...
- Chang, Han-Ting; Sharpless, K.
Barry (1996). "Catalytic
Asymmetric Aminohydroxylation (AA) of Olefins". Angew. Chem. Int. Ed. Engl. 35 (4): 451–4. doi:10...
- ISSN 1319-6103. Bodkin, J. A.; McLeod, M. D. (2002). "The
Sharpless asymmetric aminohydroxylation". J. Chem. Soc.,
Perkin Trans. 1. 2002 (24): 2733–2746. doi:10.1039/b111276g...
-
asymmetric dihydroxylation Sharpless epoxidation Sharpless oxyamination or
aminohydroxylation Shenck ene
reaction Shi
epoxidation Shiina esterification Shiina macrolactonization...
- transformations, such as Carbon-Boron bond formation,
carbene insertion, and
aminohydroxylation by
evolving the
sequence context of the
corresponding ArMs. As the...
-
reactions – the
sharpless asymmetric epoxidation, dihydroxylation, and
aminohydroxylation –
which have
revolutionized organic chemistry by
transforming asymmetric...
