Abstract
3-Formyl-2-acetylenyl-1-methylindole oximes readily undergo intramolecular heterocyclization with closure of a pyridine ring and formation of substituted γ-carboline N-oxides.
| Original language | English |
|---|---|
| Pages (from-to) | 2383-2385 |
| Number of pages | 3 |
| Journal | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science |
| Volume | 33 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - 1 Nov 1984 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Chemistry(all)
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Cyclizaticn of 3-formyl-2-acetylenylindole oximes. / Prikhod'ko, T. A.; Vasilevskii, S. F.; Shvartsberg, M. S.
In: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, Vol. 33, No. 11, 01.11.1984, p. 2383-2385.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Cyclizaticn of 3-formyl-2-acetylenylindole oximes
AU - Prikhod'ko, T. A.
AU - Vasilevskii, S. F.
AU - Shvartsberg, M. S.
PY - 1984/11/1
Y1 - 1984/11/1
N2 - 3-Formyl-2-acetylenyl-1-methylindole oximes readily undergo intramolecular heterocyclization with closure of a pyridine ring and formation of substituted γ-carboline N-oxides.
AB - 3-Formyl-2-acetylenyl-1-methylindole oximes readily undergo intramolecular heterocyclization with closure of a pyridine ring and formation of substituted γ-carboline N-oxides.
UR - http://www.scopus.com/inward/record.url?scp=0037694382&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0037694382&partnerID=8YFLogxK
U2 - 10.1007/BF00948858
DO - 10.1007/BF00948858
M3 - Article
AN - SCOPUS:0037694382
VL - 33
SP - 2383
EP - 2385
JO - Russian Chemical Bulletin
JF - Russian Chemical Bulletin
SN - 0568-5230
IS - 11
ER -