-
compounds of
empirical formula AlR3 and AlR1.5Cl1.5 exist. The
aluminium trialkyls and
triaryls are reactive, volatile, and
colorless liquids or low-melting...
-
phosphine oxides. Qualitatively, the
rates of
oxidation are
higher for
trialkyl vs triarylphosphines.
Faster still are
oxidations using hydrogen peroxide...
-
dialkyl phosphate during pregnancy appears to
increase the risk of ADHD. In
Trialkyl phosphates, all
three hydrogens in
phosphoric acid are
replaced by alkyl...
- The Barton–McCombie
deoxygenation is an
organic reaction in
which a
hydroxy functional group in an
organic compound is
replaced by a
hydrogen to give an...
- deprotonated: AsH3 + NaNH2 → NaAsH2 + NH3 Upon
reaction with the
aluminium trialkyls, AsH3
gives the
trimeric [R2AlAsH2]3,
where R = (CH3)3C. This reaction...
-
temperature and pressure, or by
thermal decomposition of a
mixture of a
trialkyl indium compound and phosphine. The
application fields of InP
splits up...
- Jacobsen's
catalysts R = Alkyl, O-alkyl, O-
trialkyl Best
Jacobsen catalyst: R = tBu...
- carbon; typically, they are
organic derivatives of
borane (BH3), as in the
trialkyl boranes.
Organoboranes and -borates
enable many
chemical transformations...
- 26896-20-8.
Components of the
mixture are
acids with the
common property of a "
trialkyl acetic acid"
having three alkyl groups at
carbon two, including: 2,2,3...
-
retention of
stereochemistry (in reality, the
reaction occurs via the
trialkyl borate B(OR)3,
rather than the
monoalkyl borinic ester BH2OR). The 'H'...
