- In
organic chemistry,
regioselectivity is the
preference of
chemical bonding or
breaking in one
direction over all
other possible directions. It can often...
- used in the
industrial synthesis of 3-hydroxy-2-naphthoic acid; the
regiochemistry of the
carboxylation in this case is
sensitive to temperature. The Kolbe–Schmitt...
-
component sugars are the same (e.g., glucose),
different bond
combinations (
regiochemistry) and
stereochemistry (alpha- or beta-)
result in
trisaccharides that...
-
about the
stereochemistry of the
newly formed alkene, but only the
regiochemistry of the
elimination reaction.
While effective at
predicting the favored...
- Na+, etc.). For
unsymmetrical ketones,
methods exist to
control the
regiochemistry of the deprotonation. The
deprotonation of
carbon acids can proceed...
- In
organic chemistry, free-radical
addition is an
addition reaction which involves free radicals.
These reactions can
happen due to the free
radicals having...
-
component sugars are the same (e.g., glucose),
different bond
combinations (
regiochemistry) and
stereochemistry (alpha- or beta-)
result in
disaccharides that...
- strongly, and
result in the most
energetically favourable bond formation.
Regiochemistry in
DAINV reactions can be
reliably predicted in many cases. This can...
- BMS and borane-THF are equivalent. The
stoichiometry and
idealized regiochemistry of
hydroboration of
terminal alkenes follows: BH3 + 3 RCH=CH2 → B(CH2−CH2R)3...
- In
organic chemistry, the
Murai reaction is an
organic reaction that uses C-H
activation to
create a new C-C bond
between a
terminal or
strained internal...
