-
highly branched polyethylene with
acenaphthenediimine nickel chloride/
diethylaluminum chloride catalyst".
Chinese Journal of
Polymer Science 2006, 24 (5)...
- 276863". Sigma-Aldrich.
Retrieved December 9, 2012. Nagata, W (1988). "
Diethylaluminum cyanide".
Organic Syntheses. VI: 307. doi:10.15227/orgsyn.052.0090...
- CuC≡N → ArC≡N + N2 + Cu+ A
commercial source for the
cyanide group is
diethylaluminum cyanide Et2AlCN
which can be
prepared from
triethylaluminium and HCN...
- ch1. ISBN 9780470504437.
Wataru Nagata and
Yoshioka Mitsuru (1988). "
Diethylaluminum Cyanides".
Organic Syntheses;
Collected Volumes, vol. 6, p. 436. TEA...
-
lithium amides, are
prepared from the
corresponding lithium amides and
diethylaluminum chloride.
Reactions are
usually carried out at 0 °C in an
inert atmosphere...
- Trimethyl(phenylthiomethyl)silane (C10), 2-bromobenzaldehyde (C3 to C9),
diethylaluminum cyanide (C19) and
trimethylsilylmethyl bromide (C20) Ring A synthesis...
-
unsaturated carbonyls. In the
Nagata reaction the
cyanide source is
diethylaluminum cyanide. The
Gilman reagent is an
effective nucleophile for 1,4-additions...
- "Asymmetric
Strecker Synthesis using Enantiopure Sulfinimines and
Diethylaluminum Cyanide: The
Alcohol Effect".
Journal of
Organic Chemistry. 61 (2):...
- process, such as the
transalkylation of
styrene to form 2-phenylethanol.
Diethylaluminum hydride can be emplo**** in
place of triethylaluminium.
Guerbet reaction...
-
Ziegler catalysis uses
nickel as a catalyst. In
addition it uses
diethylaluminum ethoxide,
phenylacetylene and
triethylaluminium It
converts ethylene...
