Circular dichroism of guaianolides and the products of their amination View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1984-11-01

AUTHORS

G. P. Moiseeva, I. M. Yusupova, Sh. Z. Kasymov, M. I. Yusupov

ABSTRACT

The presence of an α-oriented hydroxy group at C8 in a guaianolide promotes the stereospecificity of the amination of an exomethylene bond linked with the γ-lactone grouping. The addition of morphiline and of piperidine to the exomethylene bond of the lactone ring of a guaianolide containing an α-oriented hydroxy group at C8 takes place with the preferential formation of the 11S isomer. More... »

PAGES

683-685

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00580022

DOI

http://dx.doi.org/10.1007/bf00580022

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1034744758


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