-
straightforward reactions.
Lutidine comes in
several isomers: 2,3-
Lutidine (2,3-dimethylpyridine) 2,4-
Lutidine (2,4-dimethylpyridine) 2,5-
Lutidine (2,5-dimethylpyridine)...
- dimethyl-substituted
derivative of pyridine, all of
which are
referred to as
lutidines. It is a
colorless liquid with
mildly basic properties and a pungent,...
- dimethyl-substituted
derivatives of pyridine, all of
which are
referred to as
lutidines. It is a
colorless liquid with
mildly basic properties and a pungent,...
-
lutidines. It is a
colorless liquid with
mildly basic properties and a
pungent odor. The
compound is a
precursor to the drug omeprazole. 3,5-
Lutidine...
-
related cations are
known involving substituted pyridines, e.g. picolines,
lutidines, collidines. They are
prepared by
treating pyridine with acids. As pyridine...
-
formula C7H9N may
refer to:
Benzylamine Lutidines (dimethylpyridines) 2,4-
Lutidine 2,6-
Lutidine 3,5-
Lutidine N-Methylaniline
Toluidines o-Toluidine m-Toluidine...
-
Trifluoromethylation using CF3I and triethylborane. The base is 2,6-
lutidine...
- pyridine, and
various alkyl homologues of pyridine, such as
picoline and
lutidine.
Water concerns are
sensitive issues in arid regions, such as the western...
-
trifluoromethanesulfonate (TMSOTf) and base (i.e. pyridine, triethylamine, or 2,6-
lutidine) in
dichloromethane TMSCl and
lithium sulfide (Li2S) in
acetonitrile TMS...
-
using trimethylsilyl trifluoromethanesulfonate and
triethylamine or 2,6-
lutidine.
TMSOTf is also a
useful reagent to
replace metal-halogen
bonds with a...
