1970
DOI: 10.1055/s-1970-21620
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The Isomerization of Olefins Part II. Thermal and Catalytic lsomerization of Olefins using Acids, Metals, Metal Complexes, or Boron Compounds as Catalysts

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Cited by 65 publications
(20 citation statements)
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“…The results are shown in this section. isomerization transformations of alkenes in the presence of acidic catalysts [47]. Double-bond migration and cis/trans isomerization are facile transformations that can take place under mild conditions and they have been subject of intensive research to investigate the acidity of different catalysts [31, 47 -61].…”
Section: Metathesis Properties Of Ni/almcm-41 Catalystsmentioning
confidence: 99%
“…The results are shown in this section. isomerization transformations of alkenes in the presence of acidic catalysts [47]. Double-bond migration and cis/trans isomerization are facile transformations that can take place under mild conditions and they have been subject of intensive research to investigate the acidity of different catalysts [31, 47 -61].…”
Section: Metathesis Properties Of Ni/almcm-41 Catalystsmentioning
confidence: 99%
“…Olefins are susceptible to isomerization triggered by acids and bases, as well as by metallic catalysts . On heterogeneous catalysts, these properties may be inherent to the support, viz.…”
Section: Opportunities Of Heterogeneous Grubbs Catalystsmentioning
confidence: 99%
“…For their importance in pharmacology, see: Fü lö p et al (2001). For the reactivity of the cycloocta-1,5-diene in basic medium, see: Huber et al (1969Huber et al ( , 1970. For the preparation of analogous unsaturated cyclooctane esters, see: Garrido et al (2008).…”
Section: Related Literaturementioning
confidence: 99%
“…In our research group there has been an enormous interest in the synthesis of conjugated unsaturated esters used as starting material in the Michael addition of enantiomerically pure lithium amides (Davies et al, 2005) as a base tool in the asymmetric synthesis of β-amino acids and alkaloids because of their interest and value in the development of biologically active compounds for the pharmacology industry (Fülöp et al, 2001). Considering that the reactivity of the cycloocta-1,5-diene is very peculiar, highlighting its trend in basic medium to conjugate its double bonds (Huber et al, 1969) because of the greater thermodynamic stability (Huber et al, 1970), is necessary and important to establish the exact structure in this class of unsaturated rings. This conjugation was determined previously for an isomer of compound 1 (tert-butyl cyclooct-1,7-dienecarboxylate) (Garrido et al, 2008) and herein for compound 1 (tert-butylcyclooct-1,3dienecarboxylate) by R-X spectroscopy of compound 6 which confirms unequivocally its configuration and structure.…”
Section: Data Collectionmentioning
confidence: 99%