- In chemistry,
stereospecificity is the
property of a
reaction mechanism that
leads to
different stereoisomeric reaction products from
different stereoisomeric...
-
typically do not have an
asymmetric center, so they are
usually not
stereospecific.
Recently there has been an
increase in the
emergence of terminally...
- general,
glycerophospholipids use an "sn" notation,
which stands for
stereospecific numbering. When the
letters "sn"
appear in the nomenclature, by convention...
- one or a
combination of the following: Ketoreductase- Uses
NADPH to
stereospecifically reduce it to a
hydroxyl group Dehydratase-
Catalyzes the
removal of...
-
demercuration part of the
reaction involves free
radical mechanism and is not
stereospecific, i.e. H and OH may be syn or anti to each other.
Oxymercuration followed...
-
transition state. Stereochemistry: 1,3-dipolar
cycloadditions are
always stereospecific with
respect to the
dipolarophile (i.e., cis-alkenes
giving syn-products)...
-
Despite the fact that the vast
majority of Diels–Alder
reactions exhibit stereospecific, syn
addition of the two components, a
diradical intermediate has been...
-
sometimes giving almost exclusively one product. The
rearrangement occurs stereospecifically for
ketoximes and N-chloro/N-fluoro imines, with the
migrating group...
-
reaction rate of a
chemical reaction.
Stereochemistry is
involved in:
stereospecific reactions stereoselective or
asymmetric reactions racemisation processes...
-
Styrene oxide is an
epoxide derived from styrene. It can be
prepared by
epoxidation of
styrene with
peroxybenzoic acid, in the
Prilezhaev reaction: Styrene...
