- reaction.
Tosylhydrazones can be
reduced to the
corresponding alkanes with
reagents such as
sodium borohydride and borane.
Tosylhydrazone salts can react...
-
preformed N-
tosylhydrazones are used.
Barluenga and
coworkers also
developed metal-free
reductive coupling methodology of N-
tosylhydrazones with boronic...
-
catecholborane to
reduce α,β-unsaturated
tosylhydrazones. The
mechanism of NaBH3CN
reduction of α,β-unsaturated
tosylhydrazones has been
examined using deuterium-labeling...
- 1021/ar00086a004. Shapiro,
Robert H.; Heath,
Marsha J. (1967). "
Tosylhydrazones. V.
Reaction of
Tosylhydrazones with
Alkyllithium Reagents. A New
Olefin Synthesis"...
- THC-O-acetate
Srebnik M,
Mechoulam R (1984). "Reactions of
cannabinoid tosylhydrazones:
Stereochemical aspects". Tetrahedron. 40 (19): 3839–3843. doi:10...
- the
carbonylation of α‐diazocarbonyl
compounds and a
variety of N‐
tosylhydrazones catalysed by Co(II)–porphyrin
metalloradicals leading to the formation...
- doi:10.1351/goldbook.H02879 Shapiro,
Robert H. (1976). "Alkenes from
Tosylhydrazones". Org. React. 23 (3): 405–507. doi:10.1002/0471264180.or023.03. ISBN 0471264180...
-
Diazo compounds are
intermediates in the Bamford–Stevens
reaction of
tosylhydrazones to alkenes,
again with a
carbene intermediate: In the Doyle–Kirmse...
-
single ketone can also be
converted to the
corresponding alkene via its
tosylhydrazone,
using sodium methoxide (the Bamford–Stevens reaction) or an alkyllithium...
-
Organic Syntheses;
Collected Volumes, vol. 8, p. 612. X.
Creary (1990). "
Tosylhydrazone Salt Pyrolyses: Phenydiazomethanes".
Organic Syntheses;
Collected Volumes...
