⌘+K

Pulse Explore Communities Researchers Journals

Home Communities Explore

January 17, 1989Liebigs Annalen der Chemie

HPLC‐Trennung verschiedener α‐substituierter γ‐Lactone und 1,3‐Dioxolan‐4‐one an ChiraSpher

Uwe Gerlach Thomas Haubenreich Siegfried Hünig Norman Klaunzer

View at Publisher

Ask AI

Bookmark

Share

Abstract

HPLC Separation of Various α‐Substituted γ‐Lactones and 1,3‐Dioxolan‐4‐ones on ChiraSpher Various α‐substituted 1,3‐dioxolan‐4‐ones and α‐substituted γ‐lactones are resolved by analytical HPLC on the chiral phase ChiraSpher®, the enhanced range of application of which should be useful for the separation of similar compounds.

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Gerlach et al. (1989) studied this question.

synapsesocial.com/papers/6aa229b94cf61d0c7107e96b https://doi.org/10.1002/jlac.198919890122

View at Publisher

Ask AI

Bookmark

Share

Keep reading

Synapse has enriched 5 related papers. Consider them for comparative context:

1Enantiomer‐Differentiation Induced by an Enantiomeric Excess during Chromatography with Achiral PhasesOriginal Research · 1985 · 108 citations
2Analytic and preparative resolution of recemic γ‐ and δ‐lactones by chromatography on cellulose triacetate. Relationship between elution order and absolute configurationOriginal Research · 1987 · 58 citations
3Supramolekulare Phosphorylierung kationischer Alkohole mit 3‐Arylindol‐4‐carboxamidin‐StrukturLiebigs Annalen der Chemie · Wed,
4Axiceramide A and B, Two Novel tri‐α‐Glycosylceramides from the Marine Sponge Axinella sp.Liebigs Annalen der Chemie · Wed,
5Longiside, a Novel Digalactosylceramide from the Caribbean Sponge Agelas longissimaLiebigs Annalen der Chemie · Wed,

More from Liebigs Annalen der Chemie

The Redox Pair Vitamin E and Vitamin C, A 13C‐NMR StudyWed,
Synthesis of Medium and Large Ring Compounds, XXXVIII. Ring Enlargement of Cyclodecanone by a Chiral Building Block: Synthesis and Olfactory Properties of (12R)‐(+)‐12‐Methyl‐13‐TridecanolideWed,
Synthesis of (3R)‐3‐Hydroxy‐2‐Hexanone, (2R,3R)‐2,3‐hexanediol and (2S,3R)‐2,3‐hexanediol, the Male Sex Pheromone of Hylotrupes bajulus and Pyrrhidium sanguineum (cerambycidae)Wed,
Boulton‐Katritzky Rearrangement of 5‐(cyanoimino)‐1,2,4‐ThiadiazolinesWed,
Nitro Ketones in Organic Synthesis: A New, Short Synthesis of Racemic trans‐2‐methyl‐1,7‐dioxaspiro[5.5]undecane, trans, trans‐ and trans, cis‐2,8‐dimethyl‐1,7‐dioxaspiro[5.5]undecane by Henry reactionWed,