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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 |