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Silylation is the
introduction of one or more (usually)
substituted silyl groups (R3Si) to a molecule.
Silylations are core
methods for
production of...
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Silyl ethers are a
group of
chemical compounds which contain a
silicon atom
covalently bonded to an
alkoxy group. The
general structure is R1R2R3Si−O−R4...
- In
organosilicon chemistry,
silyl enol
ethers are a
class of
organic compounds that
share the
common functional group R3Si−O−CR=CR2,
composed of an enolate...
- "super"
silyl groups of
which there exist two varieties: A
silicon group connected to
three trimethylsilyl groups makes a tri(trimethylsilyl)
silyl group...
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Silyl-modified
polymers (SMP; also silane-modified polymers, modified-silane polymers, MS polymers, silane-terminated polymers, etc.) are
polymers terminating...
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prepared by
hydrolysis of
silyl chlorides: R 3SiCl + H2O → R 3SiOH + HCl Less
frequently silanols are
prepared by
oxidation of
silyl hydrides, a
reaction that...
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coupling of a nucleophilic,
heterocyclic base with an
electrophilic sugar. The
silyl-Hilbert-Johnson (or Vorbrüggen) reaction,
which employs silylated heterocyclic...
- chemistry,
transition metal silyl complexes describe coordination complexes in
which a
transition metal is
bonded to an
anionic silyl ligand,
forming a metal-silicon...
- alkali. The
alkoxysilanes (
silyl ethers) of the type R3Si(OR') are slow to hydrolyze.
Compared to the
silyl ethers,
silyl acetates are
faster to hydrolyze...
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converted to the
trichlosilylbenzyl compound. In the
second step, the
benzylic silyl derivative is
converted to the
toluene derivative with base. Trichlorosilane...
