194934-66-2Relevant academic research and scientific papers
Frogolide – An Unprecedented Sesquiterpene Macrolactone from Scent Glands of African Frogs
Menke, Markus,Melnik, Kristina,Peram, Pardha S.,Starnberger, Iris,H?dl, Walter,Vences, Miguel,Schulz, Stefan
, p. 2651 - 2656 (2018)
Some amphibians use chemical signals in addition to optical and acoustical signals to transmit information. Males of mantellid frogs from Madagascar and hyperoliid frogs from Africa emit complex, species- and sex-specific bouquets of volatiles from their femoral or gular glands. We report here on the identification, synthesis, and determination of the absolute configuration of a macrocyclic lactone occurring in several species of both families, (S)-3,7,11-dodec-6,10-dien-12-olide (S-14, frogolide). Macrolides are a preferred compound class of frog volatiles. Nevertheless, frogolide is the first macrocyclic lactone obviously derived from the terpene pathway, in contrast to known frog macrolides that are usually formed via the fatty acid biosynthetic pathway.
Identification and Composition of Clasper Scent Gland Components of the Butterfly Heliconius erato and Its Relation to Mimicry
Darragh, Kathy,Ehlers, Stephanie,H?tling, Susan,Harig, Tim,Jiggins, Chris D.,Schulz, Stefan,Stell, Matthew,Szczerbowski, Daiane
, p. 3300 - 3313 (2021/10/12)
The butterfly Heliconius erato occurs in various mimetic morphs. The male clasper scent gland releases an anti-aphrodisiac pheromone and additionally contains a complex mixture of up to 350 components, varying between individuals. In 114 samples of five different mimicry groups and their hybrids 750 different compounds were detected by gas chromatography/mass spectrometry (GC/MS). Many unknown components occurred, which were identified using their mass spectra, gas chromatography/infrared spectroscopy (GC/IR)-analyses, derivatization, and synthesis. Key compounds proved to be various esters of 3-oxohexan-1-ol and (Z)-3-hexen-1-ol with (S)-2,3-dihydrofarnesoic acid, accompanied by a large variety of other esters with longer terpene acids, fatty acids, and various alcohols. In addition, linear terpenes with up to seven uniformly connected isoprene units occur, e. g. farnesylfarnesol. A large number of the compounds have not been reported before from nature. Discriminant analyses of principal components of the gland contents showed that the iridescent mimicry group differs strongly from the other, mostly also separated, mimicry groups. Comparison with data from other species indicated that Heliconius recruits different biosynthetic pathways in a species-specific manner for semiochemical formation.
METHOD FOR PRODUCING OPTICALLY ACTIVE 2,3-DIHYDROFARNESAL
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Paragraph 0012; 0098-0099, (2017/07/08)
PROBLEM TO BE SOLVED: To provide a synthetic intermediate useful for obtaining optically active 2,3-dihydrofarnesal high in chemical purity and optical purity, and a satisfactorily efficient method for producing the intermediate. SOLUTION: Provided is optically active farnesyl enamine represented by formula (4) (*denotes an asymmetric carbon atom; R1 and R2 respectively independently denote H, a substituted/unsubstituted 1-20C alkyl group, a substituted/unsubstituted 3-8 membered-ring alicyclic group, a substituted/unsubstituted 6-15C aryl group; a substituted/unsubstituted 2-15C heterocyclic group or a substituted/unsubstituted 7-12C aralkyl group; and R1 and R2 are not simultaneously H or R1 and R2 may be coupled to form a ring). SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT
METHOD FOR PRODUCING OPTICALLY ACTIVE 2,3-DIHYDROFARNESAL
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, (2015/09/22)
A method for producing an optically active 2,3-dihydrofarnesal of formula (1) is disclosed. The method includes subjecting β-farnesene f formula (2) to amination in the presence of a lithium salt of an amine to obtain (2E)-farnesyl allylamine of general formula (3); subjecting the (2E)-farnesyl allylamine to asymmetric isomerization to obtain an optically active farnesyl enamine of general formula (4); and subjecting the optically active farnesyl enamine to solvolysis:
FRAGRANCE COMPOSITION
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, (2015/09/22)
The present invention relates to: a fragrance composition containing (3S)-(6E)-2,3-dihydrofarnesal having a chemical purity of 90 mass% or more and an optical purity of 50% e.e. or more; a cosmetic product containing the fragrance composition; and a method for improving an aroma using the fragrance composition.
METHOD FOR PRODUCING OPTICALLY ACTIVE 2,3-DIHYDROFARNESAL
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, (2015/07/22)
A method for producing an optically active 2,3-dihydrofarnesal represented by formula (1): the method comprising: subjecting β-farnesene represented by formula (2) to amination in the presence of a lithium salt of an amine: to obtain (2E)-farnesyl allylamine represented by general formula (3): subsequently subjecting to asymmetric isomerization to obtain an optically active farnesyl enamine represented by general formula (4): and subjecting the optically active farnesyl enamine to solvolysis, wherein R1, R2, and * are as defined in claims of the present application.
Asymmetric counteranion-directed catalysis
Mayer, Sonja,List, Benjamin
, p. 4193 - 4195 (2007/10/03)
(Chemical Equation Presented) Exceedingly high enantioselectivity in a catalytic reaction can be realized even when the chirality resides only in the counteranion of the catalyst. A salt (1) composed of an achiral ammonium cation and a chiral phosphate counteranion catalyzes asymmetric transfer hydrogenations of aromatic and aliphatic α,β-unsaturated aldehydes with a Hantzsch ester in excellent enantioselectivities (see scheme).
