dc.contributor.author |
Skvortsov I. |
|
dc.contributor.author |
Kolesnikov S. |
|
dc.contributor.author |
Samitov Y. |
|
dc.contributor.author |
Shcherbakova G. |
|
dc.date.accessioned |
2018-09-14T20:07:03Z |
|
dc.date.available |
2018-09-14T20:07:03Z |
|
dc.date.issued |
1977 |
|
dc.identifier.issn |
0009-3122 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/132145 |
|
dc.description.abstract |
Mixtures of isomeric 5-, 6-, and 7-carbethoxymethyl-1,2-dihydropyrrolizines were obtained by reaction of 1,2-dihydropyrrolizines with ethyl diazoacetate. The effect of the position of the alkyl groups in the two-membered ring on the ratio of isomers in the reaction products is demonstrated. A method for the isolation of 5-carbethoxymethyl-1,2-dihydropyrrolizines from the mixtures of isomers based on the difference in their reactivities in diazo coupling is described. The preferred conformations of the two-membered rings in the 5-carbethoxymethyl-1,2-dihydropyrrolizines are judged from the PMR spectral data. © 1978 Plenum Publishing Corporation. |
|
dc.relation.ispartofseries |
Chemistry of Heterocyclic Compounds |
|
dc.title |
Research on 1-aza two-ring systems - XVI. Synthesis of 5-, 6-, and 7-carbethoxymethyl-1,2-dihydropyrrolizines and method for the isolation of 5-carbethoxymethyl-1,2-dihydropyrrolizines from mixtures with other isomers |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
8 |
|
dc.relation.ispartofseries-volume |
13 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
877 |
|
dc.source.id |
SCOPUS00093122-1977-13-8-SID34250283134 |
|