-
Silylation is the
introduction of one or more (usually)
substituted silyl groups (R3Si) to a molecule.
Silylations are core
methods for
production of organosilicon...
-
trifluoromethanesulfonic acid. It is
commonly used as a
Lewis acid catalyst, e.g. in
silylations. A
white powder, zinc
triflate is
commercially available,
though some...
-
laboratory gl****ware,
making the
surfaces more lipophilic. By the
process of
silylation,
polar functional groups such as
alcohols and
amines readily undergo reaction...
-
adulteration by
added sugars with
these methods.
Derivatization using silylation reagents is
commonly used. Also, the
proportions of di- and trisaccharides...
-
deprotection methods are too
harsh for the substrate. The
mechanism involves silylation of the
carbonyl oxygen and
elimination of tert-butyl
iodide (1), methanolysis...
- Wilson, Jake W.; Hartwig, John F. (2023). "Transition-Metal-Catalyzed
Silylation and
Borylation of C–H
Bonds for the
Synthesis and
Functionalization of...
- Volumes, vol. 8, p. 616. Kuwajima, I.; Nakamura, E.; Hashimoto, K. (1990). "
Silylation of
Ketones with
Ethyl Trimethylsilacetate: (Z)-3-Trimethylsiloxy-2-Pentene"...
-
which all have an
abundance of
hydroxyl groups.
Silanization differs from
silylation,
which usually refers to
attachment of
organosilicon groups to molecular...
-
organosilicon compounds is
found to be very
efficient and
replaced TMSCl reagent.
Silylation of
glutamic acid with
excess hexamethyldisilazane and
catalytic TMSCl...
-
Enolates can be
trapped by the
addition of
electrophiles at oxygen.
Silylation gives silyl enol ether.
Acylation gives esters such as
vinyl acetate....
