- in methanol. In the
trichloroacetimidate method of
Richard R. Schmidt, the
peracetylated O-(α-d-glucopyranyl)
trichloroacetimidate forms with 1-octanethiol...
- rearrangement.
Benzyl trichloroacetimidate is
easily accessible from
benzyl alcohol and trichloroacetonitrile.
Benzyl trichloroacetimidate is
useful as a benzylating...
-
Bucher et al.
provides a way to
utilize a
fluoro oxonium ion and the
trichloroacetimidate to
encourage B
stereoselectivity through the
gauche effect. This...
-
catalyzed reaction of
benzyl alcohol upon
trichloroacetonitrile yields a
trichloroacetimidate. This
species has
orthogonal stability to
acetate and TBS protections...
- p-methoxybenzyl
halide (chloride or bromide) 4-methoxybenzyl-2,2,2-
trichloroacetimidate can be used to
install the PMB
group in
presence of:
Scandium (III)...
-
promoter or catalyst: The
bromide can be
activated by
silver salts, the
trichloroacetimidate with acid catalysis, and
thioglycosides with N-iodosuccinimide/triflic...
-
Thioglycoside and
trichloroacetimidate donors are used more than
others in
contemporary glycosylation methods. When it
comes to the
trichloroacetimidate method,...
- (named
after Larry Overman) is a
Claisen rearrangement of
allylic trichloroacetimidates to
allylic trichloroacetamides. The
Overman rearrangement is applicable...
- The key
reactions in this
method include aldol condensation and
trichloroacetimidate glycosylation. The
compound can also be
prepared by
reducing raspberry...
- glycosidation, use of
glycosyl acetates, thioglycosides,
glycosyl trichloroacetimidates,
glycosyl fluorides or n-pentenyl
glycosides as
glycosyl donors...
