- In
organic chemistry,
benzyl is the
substituent or
molecular fragment possessing the
structure R−CH2−C6H5.
Benzyl features a
benzene ring (C6H6) attached...
- Trnka, T.; Cerny, M. (2004). "Improved
procedure for the
selective N-
debenzylation of
benzylamines by
diisopropyl azodicarboxylate". Synthesis. 3 (3):...
- ; Murty,
Varanasi S.; Langley,
David R.; Jones, Gary B. (1990). "O-
Debenzylation of a Pyrrolo[2,1-c][1,4]benzodiazepine in the
Presence of a Carbinolamine...
-
nitro compound reduction, the
reduction of
imines and
Schiff bases and
debenzylation reactions.
Palladium on
carbon is a
common catalyst for hydrogenolysis...
-
certain porins.
Benzalkonium chloride degradation follows consecutive debenzylation, dealkylation, and
demethylation steps producing benzyl chloride, an...
- alkanes. In the laboratory,
hydrogenolysis is used in
organic synthesis.
Debenzylation is most
common and
involves the
cleavage of
benzyl ethers: R−OCH2C6H5...
-
older nitroamine high
explosives like HMX and RDX.
Illustrating the
debenzylation tendency of benzylamines, four of the
benzyl groups are
removed from...
- used as a
source of the
thiol functional group in
organic synthesis.
Debenzylation can be
effected by
dissolving metal reduction: RSCH2C6H5 + 2 H+ + 2...
-
converted upon
retention to the n-octyl-1-thio-α-d-glucopyranoside (after
debenzylation). The
reaction of d-glucose with 1-octanethiol and Olah's
reagent (70%...
- Kazuaki; Hiraiwa, Yukihiro; Yamamoto,
Hisashi (2000-01-01). "Homogeneous
Debenzylation Using Extremely Active Catalysts: Tris(triflyl)methane, Scandium(III)...
