Abstract
The trifluoroacetylation of 9-alkenylcarbazoles in pyridine takes place regio- and stereospecifically with the formation of the Β-trifluoroacetyl derivatives. The cis isomers are inert to trifluoroacetic anhydride.
| Original language | English |
|---|---|
| Pages (from-to) | 877-879 |
| Number of pages | 3 |
| Journal | Chemistry of Heterocyclic Compounds |
| Volume | 24 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - Aug 1988 |
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ASJC Scopus subject areas
- Organic Chemistry
Cite this
9-alkenylcarbazoles. 13. Trifluoroacetylation of trans- and cis-9-alkenylcarbazoles. / Moskalev, N. V.; Filimonov, V. D.; Sirotkina, E. E.
In: Chemistry of Heterocyclic Compounds, Vol. 24, No. 8, 08.1988, p. 877-879.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - 9-alkenylcarbazoles. 13. Trifluoroacetylation of trans- and cis-9-alkenylcarbazoles
AU - Moskalev, N. V.
AU - Filimonov, V. D.
AU - Sirotkina, E. E.
PY - 1988/8
Y1 - 1988/8
N2 - The trifluoroacetylation of 9-alkenylcarbazoles in pyridine takes place regio- and stereospecifically with the formation of the Β-trifluoroacetyl derivatives. The cis isomers are inert to trifluoroacetic anhydride.
AB - The trifluoroacetylation of 9-alkenylcarbazoles in pyridine takes place regio- and stereospecifically with the formation of the Β-trifluoroacetyl derivatives. The cis isomers are inert to trifluoroacetic anhydride.
UR - http://www.scopus.com/inward/record.url?scp=34249967343&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=34249967343&partnerID=8YFLogxK
U2 - 10.1007/BF00479341
DO - 10.1007/BF00479341
M3 - Article
AN - SCOPUS:34249967343
VL - 24
SP - 877
EP - 879
JO - Chemistry of Heterocyclic Compounds
JF - Chemistry of Heterocyclic Compounds
SN - 0009-3122
IS - 8
ER -