Abstract
The condensation of iodo-N-methylpyrazole-4-carboxylic acids with substituted copper acetylides proceeds with the formation of the δ-lactone ring and leads to pyrano[4,3-c]pyrazoles.
| Original language | English |
|---|---|
| Pages (from-to) | 683-685 |
| Number of pages | 3 |
| Journal | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science |
| Volume | 30 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 1 Apr 1981 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Chemistry(all)
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Condensation of iodo-N-methylpyrazole-4-carboxylic acids with copper acetylides. / Vasilevskii, S. F.; Gerasimov, V. A.; Shvartsberg, M. S.
In: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, Vol. 30, No. 4, 01.04.1981, p. 683-685.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Condensation of iodo-N-methylpyrazole-4-carboxylic acids with copper acetylides
AU - Vasilevskii, S. F.
AU - Gerasimov, V. A.
AU - Shvartsberg, M. S.
PY - 1981/4/1
Y1 - 1981/4/1
N2 - The condensation of iodo-N-methylpyrazole-4-carboxylic acids with substituted copper acetylides proceeds with the formation of the δ-lactone ring and leads to pyrano[4,3-c]pyrazoles.
AB - The condensation of iodo-N-methylpyrazole-4-carboxylic acids with substituted copper acetylides proceeds with the formation of the δ-lactone ring and leads to pyrano[4,3-c]pyrazoles.
UR - http://www.scopus.com/inward/record.url?scp=34250227037&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=34250227037&partnerID=8YFLogxK
U2 - 10.1007/BF00949744
DO - 10.1007/BF00949744
M3 - Article
AN - SCOPUS:34250227037
VL - 30
SP - 683
EP - 685
JO - Russian Chemical Bulletin
JF - Russian Chemical Bulletin
SN - 0568-5230
IS - 4
ER -