- The
Bischler–Napieralski
reaction is an
intramolecular electrophilic aromatic substitution reaction that
allows for the
cyclization of β-arylethylamides...
- The
Bischler–Möhlau
indole synthesis, also
often referred to as the
Bischler indole synthesis, is a
chemical reaction that
forms a 2-aryl-indole from an...
-
following Bischler–Napieralski
reaction produces papaverine. The Pictet–Gams
reaction and the Pictet–Spengler
reaction are both
variations on the
Bischler–Napieralski...
- Hélène
Bischler-Causse (January 3, 1932, in Bern –
February 12, 2005, in Paris) was a
French botanist and bryologist, best
known for her
research and description...
-
August Bischler (29
April 1865 – 26 May 1957) was a
Russian Empire-born
ethnic Crimea German chemist who
later emigrated to Switzerland. He discovered...
- Vilsmeier–Haack
reaction Aldehyde (via imine) POCl3,
aromatic substrate,
formamide Bischler–Napieralski
reaction Cyclic aryl
imine POCl3, SOCl2, etc.
Tautomeric chlorination...
- one-pot
synthesis using microwave irradiation.
Bartoli indole synthesis Bischler–Möhlau
indole synthesis Cadogan-Sundberg
indole synthesis ****uyama indole...
-
electrophilic substitutions to
pyrrole are the Pictet–Spengler
reaction and the
Bischler–Napieralski reaction.
Electrophilic aromatic substitutions with prochiral...
-
related reaction,
certain aryl-substituted
amides can be
cyclized using the
Bischler-Napieralski reaction. Such
reactions are
believed to
proceed via an imidoyl...
-
synthesis Biginelli reaction Bingel reaction Birch reduction Bischler–Möhlau
indole synthesis Bischler–Napieralski
reaction Biuret test
Blaise ketone synthesis...
