Z-E conformational isomerism of nerol, geraniol, and their acetates

J.W. Haan, de, L.J.M. Ven, van de

Research output: Contribution to journalArticleAcademicpeer-review

18 Citations (Scopus)
1 Downloads (Pure)

Abstract

NMR shift values indicate that geraniol has an E-conformation and nerol a Z-conformation. Thus, the shift reagent, tris(dipivalomethanato)-europium(III), is added to solns. of geraniol, nerol, geranyl acetate, and neryl acetate in CCl4 and the shift values of the C-4, C-5, and C-10 protons are examd. The opposite conformational assignments made by F. H. A. Rummens (1965) are discussed. [on SciFinder (R)]
Original languageEnglish
Pages (from-to)2703-2706
Number of pages4
JournalTetrahedron Letters
Volume12
Issue number29
DOIs
Publication statusPublished - 1971

Fingerprint Dive into the research topics of 'Z-E conformational isomerism of nerol, geraniol, and their acetates'. Together they form a unique fingerprint.

Cite this