- 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...
-
August Bischler (29
April 1865 – 26 May 1957) was a
Russian Empire-born
ethnic Crimea German chemist who
later emigrated to Switzerland. He discovered...
-
following Bischler–Napieralski
reaction produces papaverine. The Pictet–Gams
reaction and the Pictet–Spengler
reaction are both
variations on the
Bischler–Napieralski...
-
Beate Bischler (born 17 June 1968) is a
retired German Paralympic judoka who
competed in
international level events. She was a
bronze medalist at the 2004...
- 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...
-
reactions include (not exhaustive): Azide-alkyne ****sgen
cycloaddition Bischler–Napieralski
reaction Bucherer carbazole synthesis Danheiser annulation...
- Vilsmeier–Haack
reaction Aldehyde (via imine) POCl3,
aromatic substrate,
formamide Bischler–Napieralski
reaction Cyclic aryl
imine POCl3, SOCl2, etc.
Tautomeric chlorination...
-
nitrobenzene and the
former is
better since the
reaction is less violent.
Bischler-Napieralski
reaction Doebner-Miller
reaction Skraup, Z. H. (1880). "Eine...
- one-pot
synthesis using microwave irradiation.
Bartoli indole synthesis Bischler–Möhlau
indole synthesis Cadogan-Sundberg
indole synthesis ****uyama indole...
