- The Wolff–
Kishner reduction is a
reaction used in
organic chemistry to
convert carbonyl functionalities into
methylene groups. In the
context of complex...
- (posterior view)
Cutaneous innervation Dorsal root
Peripheral nerve field Kishner, Stephen. "Dermatomes Anatomy". eMedicine. Medscape.
Retrieved 2013-10-09...
- CH3C4H3S. It is a colorless,
flammable liquid. It can be
produced by Wolff-
Kishner reduction of thiophene-2-carboxaldehyde. Its
commercial synthesis involvess...
- "Scoliosis and
Spinal Curvatures". Medtronic.
Nowak JE (5
December 2019).
Kishner S (ed.). "Scheuermann Disease". Medscape.
McMaster MJ,
Singh H (October...
-
Reaction name
Product Comment Wolff–
Kishner reduction Alkane If an
aldehyde is
converted to a
simple hydrazone (RCH=NHNH2) and this is
heated with a base...
-
nickel sulfide. This
method is
milder than
either the
Clemmensen or Wolff-
Kishner reductions,
which employ strongly acidic or
basic conditions, respectively...
- phorone. The
intermediate triacetone amine is then
reduced in a Wolff-
Kishner reaction. 2,6-Dimethylpiperidine
Pempidine TEMPO ((2,2,6...
-
subsequently reduced to the
corresponding alkane substituent by
either Wolff–
Kishner reduction or
Clemmensen reduction. The net
result is the same as the Friedel–Crafts...
-
which often uses KOH and
platinum as catalysts, is also
known as the
Kishner cyclopropane synthesis after the
Russian chemist Nikolai Kischner and can...
- hexanaphthene, but this
riddle was
solved in 1895 by Markovnikov, N.M.
Kishner, and
Nikolay Zelinsky when they re****igned "hexahydrobenzene" and "hexanaphtene"...
