-
Norcarane, or bicyclo[4.1.0]heptane, is a
colorless liquid. It is an
organic compound prepared using the Simmons–Smith reaction, by the
action of diiodomethane...
- 3-Methylcyclohexene 4-Methylcyclohexene
Methylenecyclohexane Norbornane Norcarane Vinylcyclopentane This set
index page
lists chemical structure articles...
- 10.2009) Two
cyclopropanation reactions: Smith, R. D.; Simmons, H. E. "
Norcarane".
Organic Syntheses;
Collected Volumes, vol. 5, p. 855., Ito, Y.; Fujii...
- diiodomethane, and a zinc-copper
couple (as
iodomethylzinc iodide, ICH2ZnI)
yield norcarane (bicyclo[4.1.0]heptane). The Simmons–Smith
reaction is
generally preferred...
-
diiodomethane and a zinc-copper
couple reacts with
cyclohexene to give
norcarane (bicyclo[4.1.0]heptane).
Iodomethylzinc iodide may also be
generated by...
- rz011. ISBN 0-471-93623-5.
Howard H. Simmons,
Ronald D.
Smith (1973). "
Norcarane".
Organic Syntheses;
Collected Volumes, vol. 5, p. 855.
Eugene LeGoff...
- 2002). "Revisiting the
Mechanism of P450
Enzymes with the
Radical Clocks Norcarane and Spiro[2,5]octane".
Journal of the
American Chemical Society. 124 (21):...
-
chloride in a
total 70% yield.
Oxidation of a
radical clock substrate,
norcarane,
produced significant amounts of
radical rearranged products, suggesting...
