-
example in the Baeyer-Villiger reaction. In this reaction, an
oxygen is
regioselectively inserted near an
adjacent carbonyl group. In ketones, this insertion...
- LUMO. Hence,
cycloaddition gives the
substitution at the C-3
position regioselectively. For
methyl cinnamate, the two
substituents (Ph v.s. COOMe) compete...
-
charge and
creating the
final alcohol product.
Oxymercuration is very
regioselective and is a
textbook Markovnikov reaction;
ruling out
extreme cases, the...
- The Conrad–Limpach
synthesis is the
condensation of
anilines (1) with β-ketoesters (2) to form 4-hydroxyquinolines (4) via a
Schiff base (3). The overall...
-
Frontier molecular orbital theory has also been used to
explain the
regioselectivity patterns observed in Diels–Alder
reactions of
substituted systems....
-
Sharpless asymmetric dihydroxylation (also
called the
Sharpless bishydroxylation) is the
chemical reaction of an
alkene with
osmium tetroxide in the presence...
-
recent study,
Sloop investigated how
substituents would influence the
regioselectivity of the
product as well as the rate of
reaction during the rate-determining...
-
reaction produces a
regioisomeric mixture of triazoles, the lack of
regioselectivity in the
reaction is not a
major concern for most
current applications...
- Bystroem,
Styrbjoern E.; Nordberg, Ruth E. (November 1984). "Stereo- and
regioselective palladium-catalyzed 1,4-diacetoxylation of 1,3-dienes". The Journal...
- of
limonene is to carvone. The three-step
reaction begins with the
regioselective addition of
nitrosyl chloride across the
trisubstituted double bond...
