-
Nonaflate, CF3CF2CF2CF2SO−3, is the
common name
given to nonafluorobutanesulfonates, the
salts or
esters of
perfluorobutanesulfonic acid. Its uses are...
- amines, phenoxides, and enolates,
giving sulfonamides, aryl
nonaflates, and
alkenyl nonaflates, respectively. However, it is not
attacked by
water (in which...
-
mainly N-nitro
heterocyclic compounds. With aryl chlorides,
triflates and
nonaflates, ipso
nitration may also take place. The
phrase ipso
nitration was first...
-
rendering them
relatively stable. It has been
noted that
steroidal alkyl nonaflates (another
super leaving group)
generated from
alcohols and perfluorobutanesulfonyl...
-
corrosive solid. Its
conjugate base is
perfluorobutanesulfonate (also
called nonaflate)
which functions as the
hydrophobe in fluorosurfactants.
Since June 2003...
- anion.
Wikimedia Commons has
media related to Triflates.
Methyl triflate Nonaflate Trifluoromethanesulfonic acid
Metal triflimidate Comins'
reagent Lithium...
-
nonaflyl (nonafluorobutanesulfonyl) group, CF 3(CF 2) 3SO 2; ONf is the
nonaflate group Ts for
tosyl (p-toluenesulfonyl)
group (Ts is also the
symbol for...
-
September 2009). "Pd-Catalyzed
Conversion of Aryl Chlorides, Triflates, and
Nonaflates to Nitroaromatics".
Journal of the
American Chemical Society. 131 (36):...
-
excellent leaving groups, such as
triflate (trifluoromethanesulfonate) and
nonaflate (nonafluorobutanesulfonate), are
highly prone to SN1 reactivity. Utilization...
