- stereocenters,
often with a very high
degree of stereocontrol. (1)
Organostannanes are
known for
their stability, ease of handling, and
selective reactivity...
- groups, one of
which is
carried as an
organotin compound (also
known as
organostannanes). A
variety of
organic electrophiles provide the
other coupling partner...
- in
concentrated acid; the
major exception being tin acetylides. An
organostannane addition is
nucleophilic addition of an allyl-, allenyl-, or propargylstannanes...
- catalyst. This
isothioscyanate compound is a
member of a
family of
organostannanes reported by Wada and coworkers, and
elaborated upon by
Otera and coworkers...
- K. (1990). "Palladium-catalyzed
Coupling of
Vinyl Triflates with
Organostannanes: 4-tert-Butylcyclohexen-1-yl)-2-propen-1-one".
Organic Syntheses. 68:...
-
Stille (1990). "Palladium-catalyzed
Coupling of
Vinyl Triflates with
Organostannanes: 4-tert-butyl-1-vinylcyclohexene and 1-(4-tert-butylcyclohexen-1-yl)-2-propen-1-one"...
- reactions,
yielding a
substituted alcohol group.
Related reactions include organostannane additions,
Barbier reactions, and the Nozaki–Hiyama–Kishi reaction....
-
Suzuki reaction). However,
organozincs are more
reactive than both
organostannanes and
organoborates which correlates to
faster reaction times. The reaction...
- K. (1990). "Palladium-Catalyzed
Coupling of
Vinyl Triflates With
Organostannanes: 4-tert-Butyl-1-vinylcyclohexene and 1-(4-tert-Butylcyclohexen-1-yl)-2-propen-1-one"...
- 3]undecane) is a tin-based
atrane belonging to the
larger class of
organostannanes.
Though the term
stannatrane is
often used to
refer to the more commonly...
