-
Isoborneol is a
bicyclic organic compound and a
terpene derivative. The
hydroxyl group in this
compound is
placed in an exo position. The endo diastereomer...
-
compound is
placed in an endo position. The exo
diastereomer is
called isoborneol.
Being chiral,
borneol exists as enantiomers, both of
which are found...
- an
organic compound consisting of the
acetate ester or the
terpenoid isoborneol. It is a
colorless liquid with a
pleasant pine-like scent, and it is produced...
- was
first discovered in
bicyclic terpenes for
example the
conversion of
isoborneol to camphene: The
story of the
rearrangement reveals that many scientists...
- alpha-pinene is
converted to
isobornyl acetate.
Hydrolysis of this
ester gives isoborneol which can be
oxidized to give
racemic camphor. By contrast,
camphor occurs...
- YK, Jeon SJ,
Walsh PJ,
Nugent WA (2005). "(2S)-(−)-3-exo-(Morpholino)
isoborneol ((−)-MIB)".
Organic Syntheses. 82: 87.
Smith WB, Ho OC (1990). "Application...
- 92 % 49.47 % α-Terpineol 0.90% 1.08% γ-Terpineol 0.09%
Borneol 1.43%
Isoborneol 0.82% Terpinen-4-ol 4.32%
Nerol 0.20%
Lavandulol 0.78%
Terpenes / Terpene...
- -J.; Walsh, P. J.; Nugent, W. A. (2005). "(2S)-(−)-3-exo-(Morpholino)
Isoborneol".
Organic Syntheses. 82: 87. "Red-Al,
Sodium bis(2-methoxyethoxy)aluminumhydride"...
- 3-nitrobenzaldehyde is used as the oxidant, for example, in the
oxidation of
isoborneol to camphor. The
Oppenauer oxidation is used to
prepare analgesics in the...
-
Addition of
Dialkylzincs to
Aldehydes Using (2S)-(−)-3-exo-(Dimethylamino)
isoborneol [(2S)-DAIB]: (S)-1-Phenyl-1-propanol".
Organic Syntheses{{cite journal}}:...
