- substrates. Alternatively,
stannides attack organic electrophiles to give
organostannanes, e.g.:: 49 LiSnMe3 + CCl4 → C(SnMe3)4 + LiCl.
Important reactions...
- groups, one of
which is
carried as an
organotin compound (also
known as
organostannanes). A
variety of
organic electrophiles provide the
other coupling partner...
-
Organostannane addition reactions comprise the
nucleophilic addition of an allyl-, allenyl-, or
propargylstannane to an aldehyde, imine, or, in rare cases...
- Otera's catalyst,
named after ****anese
chemist Junzo Otera, is an
organostannane compound which has been used as a
transesterification catalyst. This isothioscyanate...
- reactions,
yielding a
substituted alcohol group.
Related reactions include organostannane additions,
Barbier reactions, and the Nozaki–Hiyama–Kishi reaction....
- as the
acetamide using acetic anhydride and this is
converted to the
organostannane through a Pd-catalyzed
stannylation with bis(tributyltin). The bromoquinolone...
-
Suzuki reaction). However,
organozincs are more
reactive than both
organostannanes and
organoborates which correlates to
faster reaction times. The reaction...
-
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"...
- 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...
- 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"...
