G. Uhde’s research while affiliated with Firmenich and other places

What is this page?


This page lists works of an author who doesn't have a ResearchGate profile or hasn't added the works to their profile yet. It is automatically generated from public (personal) data to further our legitimate goal of comprehensive and accurate scientific recordkeeping. If you are this author and want this page removed, please let us know.

Publications (11)


Absolute Konfiguration der enantiomeren ?-Cyclogeraniums�Uren, ?-Cyclogeraniale, ?-Jonone, ?-Jonone, ?-und ?-Carotine
  • Article

October 2004

·

21 Reads

·

25 Citations

Helvetica Chimica Acta

Richard Buchecker

·

Robert Egli

·

Helen Regel-Wild

·

[...]

·

Günther Ohloff

By chemical correlation with manool and ambrein the absolute configurations of the enantiomeric α-cyclogeranic acids, α-cyclogeranials, α-ionones and α- and ϵ-carotenes have been elucidated.


Über eine ungewöhnliche Cyclisationsreaktion bei der Umsetzung von (+)‐Epoxy‐α‐dihydrojonon mit Hydrazinhydrat

October 2004

·

31 Reads

·

21 Citations

Helvetica Chimica Acta

(+)-Epoxy-α-dihydroionone (2) is formed completely stereospecifically from (+)-α-ionone (1). Under the conditions of the Wharton reaction this epoxide gives the expected isomeric allyl alcohols 4 and 5 and, surprisingly, the bicyclic allyl alcohol 3. The structure and absolute configuration of the reaction products have been established. A common intermediate for the formation of compounds 3, 4 and 5 is probably the vinyl anion C.




Parmon, eine Phantomverbindung im Veilchenbl�ten�l

November 1972

·

10 Reads

·

34 Citations

Helvetica Chimica Acta

Das Blütenöl des Parma- sowie des Viktoria-Veilchens geörte am Anfang unseres Jahrhunderts zu den kostbarsten Ingredienzien der feinen Parfümerie. Sein Wohlgeruch faszinierte jedoch nicht nur die Noblen der damaligen Haute-Volée, sondern es regte ebenfalls in segensreiche Weise die Phantasie des Naturstoffchemikers jener Epoche an1). Der extrem hohen Herstellungskosten2) wegen ist das Veilchenblütenöl seit langem aus dem Handel verschwunden. Sicherlich liegt aus diesem Grund bis heute lediglich ein einziger Bericht über die chemische Zusammensetzung dieses ätherischen Öles vor [3].



Bestimmung der Chiralit�t der enantiomeren ?-Cyclogeraniums�uren, ?-Cyclogeraniale, ?-Jonone, ?-Jonone, ?-Carotine, ?-Carotine und verwandter Verbindungen durch chemische Verkn�pfungsreaktionen. Vorl�ufige Mitteilung

January 1969

·

6 Reads

·

55 Citations

Helvetica Chimica Acta

Die im Titel genannten enantiomeren Verbindungen sind durch chemische Reaktionen mit Ambrein und Manool verknüpft worden, so dass ihre Chiralität festgelegt ist. Damit ist zum erstenmal die Konfiguration eines chiralen Carotinoidkohlenwasserstoffes bestimmt. Das natürlich vorkommende (+)-α-Jonon hat R-Konfiguration, ebenso das natürliche (+)-α-Carotin.



Thermische Umlagerungen der Caryophyllene

January 1967

·

9 Reads

·

17 Citations

Helvetica Chimica Acta

(-)-Caryophyllen (1) lagert sich oberhalb 240° in (4S)-(+)-4,8,8-Trimethyl-4-vinyl-bicyclo[5.2.0]non-2-en (3) um, das sich über (-)-iso-Caryophyllen (2) mit seinem Diastereomeren 4 ins Gleichgewicht setzt. Die Isomerisierungen erfolgen nach dem Prinzip einer Cope-Umlagerung.


The absolute configuration of thujane

December 1966

·

33 Reads

·

39 Citations

Tetrahedron

(+)-cis- and (+)-trans-Thujane (XIV and XV) have been correlated with (+)-pulegone (IX) via (+)-pulegene (XIII). Using stereospecific reactions, the hydrocarbons of the thujane series have been linked with their oxygenated members. The absolute configurations found by Norin for these substances are in accord with our findings.Zusammenfassung(+)-cis- und (+)-trans-Thujan (XIV and XV) wird über (+)-Pulegen (XIII) mit dem (+)-Pulegon (IX) verknüpft. Durch Anwendung stereospezifischer Reaktionen können die Kohlenwasserstoffe der Thujanreihe mit ihren sauerstoffhaltigen Vertretern verbunden werden. Die von Norin für diese Verbindungsklasse angegebene absolute Konfiguration stimmt mit unserem Ergebnis überein.


Citations (7)


... The measured IR and VCD spectra of optically pure (À)-a-thujone, (þ)-b-thujone and (þ)-camphor are presented in Fig. 2. According to the literature [29,30], the absolute configurations of (À)-a-thujone and (þ)-b-thujone are respectively (1S,4R,5R)-(À)-4methyl-1-(propan-2-yl)-bicyclo-[3.1.0]-hexan-3-one and (1S,4S,5R)-(þ)-4-methyl-1-(propan-2-yl)-bicyclo-[3.1.0]-hexan-3one ...

Reference:

Analysis of the major chiral compounds of Artemisia herba-alba essential oils (EOs) using reconstructed vibrational circular dichroism (VCD) spectra: En route to a VCD chiral signature of EOs
The absolute configuration of thujane
  • Citing Article
  • December 1966

Tetrahedron

... Over the past 50 years, the chemical composition of essential oils and various concentrated extracts made from V. odorata were analyzed, including essential oils made from the flowers (Uhde and Ohloff 1972), "aerial parts" (Hammami et al. 2011), unspecified plant parts (Abdel-Rahim 2016, and leaves (Akhbari et al. 2012), as well as "absolutes" isolated from leaves (Saint-Lary et al. 2014), and an oil extracted from a "concrete" made from V. odorata leaves and flowers (Mohamed and Ghatas 2016). Aalthough essential oils are obtained through various distillation methods and are primarily composed of volatile compounds, concretes and absolutes are obtained through solvent extraction and contain nonvolatile compounds, too (Saint-Lary et al. 2016). ...

Parmon, eine Phantomverbindung im Veilchenbl�ten�l
  • Citing Article
  • November 1972

Helvetica Chimica Acta

... The question how to obtain such a hydrocarbon is also very important. It is known that the UV [10] or highhtemperature (>240°C, [9]) treatment makes it possible to rearrange caryophyllene with the formaa tion of compound (2) and its C 4 isomer. In the case of the UV treatment, the main resulting compound repp resents an isomer, where methyl and vinyl groups are located oppositely to those of compound (2). ...

Thermische Umlagerungen der Caryophyllene
  • Citing Article
  • January 1967

Helvetica Chimica Acta

... For information on the title compound as used as a key intermediate in chemical synthesis, see: Eugster et al. (1969); Naef & Decorzant (1986); Snowden et al. (1982); Fehr & Galindo (1986; Heather et al. (1976). For hydrogenbond graph-set notation, see: Etter et al. (1990); Bernstein et al. (1995). ...

Bestimmung der Chiralit�t der enantiomeren ?-Cyclogeraniums�uren, ?-Cyclogeraniale, ?-Jonone, ?-Jonone, ?-Carotine, ?-Carotine und verwandter Verbindungen durch chemische Verkn�pfungsreaktionen. Vorl�ufige Mitteilung
  • Citing Article
  • January 1969

Helvetica Chimica Acta

... For the investigation of those parameters, which are of importance for the distinction of the characteristic flavors 'fruity' and 'meaty', 35 furan derivatives were selected from the literature [14][15][16][17][18][19]. The chemical structures of these aroma compounds are depicted in Figure 1, and their exact aroma qualities are listed in Table 1. ...

Synthesis of rosefuran and dehydroelsholtzione
  • Citing Article
  • March 1968

The Journal of Organic Chemistry

... NH 4 Cl (16 mL, 20% in water) were then added to the reaction mixture, which was then cooled to room temperature. The mixture was extracted with EtOAc (70 mL × 3) and the organic phase was washed with saturated NaHCO 3 (50 mL), dried with MgSO 4 , concentrated in vacuo to give the crude product. After distillation, α-damascone (1.52 g, 72.4% yield, 97% chemical purity (GC)) was obtained as a sticky oil. ...

Über eine ungewöhnliche Cyclisationsreaktion bei der Umsetzung von (+)‐Epoxy‐α‐dihydrojonon mit Hydrazinhydrat
  • Citing Article
  • October 2004

Helvetica Chimica Acta