- 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...
- to the more
substituted carbon.
Alkene oxymercuration-demercuration
Stereospecific: Can only be anti
addition –
water kicks out the
mercury from underneath...
-
General structures of mono-, di-, and tri-acylglycerides with
names according to the
stereospecific numbering...
- Non-
stereospecific dipeptidase (EC 3.4.13.17, peptidyl-D-amino acid hydrolase, D-(or L-)aminoacyl-dipeptidase) is an enzyme. This
enzyme catalyses the...
-
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...
- of the
Wittig reaction to
permit the
stereospecific synthesis of
certain trisubstituted olefins.
Stereospecific synthesis of α-santalol". J. Am. Chem...
- In
molecular biology, D-
stereospecific aminopeptidase (D-aminopeptidase) EC 3.4.11.19 is an
enzyme which catalyses the
release of an N-terminal D-amino...
-
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...
