- 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...
- 660410129. Matsumoto, T.; Ichihara, A.; Ito, N. (1969). "A simple,
stereospecific synthesis of dl-muscarine and dl-allomuscarine". Tetrahedron. 25 (24):...
-
attaching to the less-substituted carbon. The
reaction thus
provides a more
stereospecific and
complementary regiochemical alternative to
other hydration reactions...
- 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...
- of the
Wittig reaction to
permit the
stereospecific synthesis of
certain trisubstituted olefins.
Stereospecific synthesis of α-santalol". J. Am. Chem...
- to each other.
Shown below is an
example of
regioselectivity and
stereospecificity of the
oxymercuration reaction with
substituted cyclohexenes. A bulky...
- Savin–Norov
machine gun
Space Network, a NASA
relay satellite system Stereospecific numbering in
compounds such as
glycerophospholipids Sthene, an obsolete...
