- acid-catalyzed
rearrangement reaction and ring-closing
reaction to
tetrahydrocarbazole. In one modification, both
steps are
rolled into one by carrying...
- S2CID 39252411.
Edelson J,
Benziger DP (1980). "Disposition of a
series of
tetrahydrocarbazoles". Drug
Metabolism Reviews. 11 (2): 263–89. doi:10.3109/03602538008994027...
- Borsche–Drechsel
cyclization is a
chemical reaction used to
synthesize tetrahydrocarbazoles by the acid-catalyzed
cyclization of
cyclohexanone arylhydrazones...
-
Identifiers IUPAC name (+)-(R)-3-Methylamino-6-carboxamido-1,2,3,4-
tetrahydrocarbazole CAS
Number 158747-02-5 Y succinate: 158930-17-7 Y
PubChem CID 77992...
-
Ivanov PY,
Neustroeva VD,
Nyrkova VG,
Pershin GN,
Shvedov VI (1986). "
Tetrahydrocarbazole derivatives and
their antitubercular activity in vitro. I. N-Substituted...
-
synthetic strategy used a Bischler-Napieralski
reaction to form the
tetrahydrocarbazole portion of Reserpine. The
subsequent imine intermediate was treated...
-
Komlossy J (June 1976). "Cycloalkanoindoles. 2. 1-Alkyl-1,2,3,4-
tetrahydrocarbazole-1-e****ines and
related compounds.
Potential antidepressants"....
