- In chemistry,
stereospecificity is the
property of a
reaction mechanism that
leads to
different stereoisomeric reaction products from
different stereoisomeric...
- The
rearrangement of
aldoximes occurs with
stereospecificity in the gas
phase and
without stereospecificity in the
solution phase. A few methodologies...
- to each other.
Shown below is an
example of
regioselectivity and
stereospecificity of the
oxymercuration reaction with
substituted cyclohexenes. A bulky...
- general,
glycerophospholipids use an "sn" notation,
which stands for
stereospecific numbering. When the
letters "sn"
appear in the nomenclature, by convention...
- in
impaired cycloaddition stereospecificity.
These results altogether confirm that 1,3-dipolar
cycloaddition is
stereospecific,
giving retention of both...
- In
organic chemistry, an
electrocyclic reaction is a type of pericyclic,
rearrangement reaction where the net
result is one pi bond
being converted into...
- 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...
-
supported with com****tional evidence) on the
grounds that the
observed stereospecificity does not rule out a two-step
addition involving an
intermediate that...
- classical, non-classical, and
hybrid synthetic cannabinoids have
stereospecificity (one
stereoisomer is
usually much more
potent than the other(s))....
- to the more
substituted carbon.
Alkene oxymercuration-demercuration
Stereospecific: Can only be anti
addition –
water kicks out the
mercury from underneath...
