-
Vicinal difunctionalization refers to a
chemical reaction involving transformations at two
adjacent centers (most
commonly carbons). This transformation...
-
carbon atoms (i.e., in a 1,2-relationship). It may
arise from
vicinal difunctionalization. For example, the
molecule 2,3-dibromobutane
carries two vicinal...
- The Liebeskind–Srogl
coupling reaction is an
organic reaction forming a new carbon–carbon bond from a
thioester and a
boronic acid
using a
metal catalyst...
-
arenes to
afford organothallium(III) derivatives. It is also used to
difunctionalize alkenes. For example,
alcohol solutions of this
reagent convert simple...
- with
Raney nickel affords butane. When
coupled with the easy 2,5-
difunctionalization of thiophene,
desulfurization provides a
route to 1,4-disubstituted...
-
Richard R. (1991). "Living Ring-Opening
Metathesis Polymerization of 2,3-
Difunctionalized 7-Oxanorbornenes and 7-Oxanorbornadienes by Mo(CHCMe2R)(N-2,6-C6H3-i-Pr2)(O-t-Bu)2...
- keto-enol
tautomerism to the
saturated carbonyl compound. In
vicinal difunctionalization the
proton is
replaced by
another electrophile.
Conjugated carbonyls...
-
Conversion of
butadiene to 1,10-
difunctionalized decanes...
-
Synthesis of 2,4-
difunctionalized tellurophenes....
- They are
traditionally produced in
modest or poor
yields from 1,3-
difunctionalized alkanes. One
example is the
reaction of
trimethylene carbonate and...
