- In chemistry,
stereospecificity is the
property of a
reaction mechanism that
leads to
different stereoisomeric reaction products from
different stereoisomeric...
- general,
glycerophospholipids use an "sn" notation,
which stands for
stereospecific numbering. When the
letters "sn"
appear in the nomenclature, by convention...
-
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...
-
Styrene oxide is an
epoxide derived from styrene. It can be
prepared by
epoxidation of
styrene with
peroxybenzoic acid, in the
Prilezhaev reaction: Styrene...
-
reaction rate of a
chemical reaction.
Stereochemistry is
involved in:
stereospecific reactions stereoselective or
asymmetric reactions racemisation processes...
-
toxic than brucine. In
chemical synthesis, it can be used as a tool for
stereospecific chemical syntheses. Brucine's name
derives from this of the
genus Brucea...
-
General structures of mono-, di-, and tri-acylglycerides with
names according to the
stereospecific numbering...
- classical, non-classical, and
hybrid synthetic cannabinoids have
stereospecificity (one
stereoisomer is
usually much more
potent than the other(s))....
-
transition state. Stereochemistry: 1,3-dipolar
cycloadditions are
always stereospecific with
respect to the
dipolarophile (i.e., cis-alkenes
giving syn-products)...
- to the more
substituted carbon.
Alkene oxymercuration-demercuration
Stereospecific: Can only be anti
addition –
water kicks out the
mercury from underneath...
