- In
organic chemistry,
regioselectivity is the
preference of
chemical bonding or
breaking in one
direction over all
other possible directions. It can often...
- ethers,
particularly those with an
adjacent carbonyl group, can be
regioselectively demethylated using magnesium iodide etherate. An
example of this being...
- of
limonene is to carvone. The three-step
reaction begins with the
regioselective addition of
nitrosyl chloride across the
trisubstituted double bond...
- has been
invoked to
explain selectivity in a
variety of stereo- and
regioselective reactions. The
relationship between the (apparent) rate
constants and...
-
charge and
creating the
final alcohol product.
Oxymercuration is very
regioselective and is a
textbook Markovnikov reaction;
ruling out
extreme cases, the...
- Niljianskul, Nootaree; Buchwald,
Stephen L. (23
October 2013). "Enantio- and
Regioselective CuH-Catalyzed
Hydroamination of Alkenes".
Journal of the
American Chemical...
-
distinguish between very
similar substrate molecules to be chemoselective,
regioselective and stereospecific. Some of the
enzymes showing the
highest specificity...
- of
carboboration are 1,1 and 1,2 carboboration,
which differ in the
regioselectivity of the
incoming carbon group. 1,1
carboboration delivers both the carbon-carbon...
-
Immobilized Candida antarctica lipase can be used to
catalyze the
regioselective acylation of flavonoids.
Phytochemical List of
antioxidants in food...
-
Sharpless asymmetric dihydroxylation (also
called the
Sharpless bishydroxylation) is the
chemical reaction of an
alkene with
osmium tetroxide in the presence...
