122313-77-3

Upstream product

• 57706-89-5 (E)-3,7-dimethylocta-2,6-dien-1-yl phenylcarbamate 

Downstream Products

• 136937-06-9 (6S,2E)-6-Acetoxy-7-hydroxy-3,7-dimethyloct-2-en-1-yl N-Phenylcarbamate 
• 122313-80-8 (6R,2E)-6,7-epoxy-3,7-dimethyl-2-octen-1-yl phenylcarbamate 
• 41720-60-9 trans-linalool oxide 
• 23007-29-6 cis-5-ethenyltetrahydro-α,α,5-trimethyl-2-furan methanol 
• 122313-79-5 (6S,2E)-6,7-dihydroxy-6,7-O-isopropylidene-3,7-dimethyl-2-octen-1-yl phenylcarbamate 
• 61262-94-0 (6S)-5,6-dihydroxy-5,6-O-isopropylidene-6-methylheptan-2-one 
• 61262-97-3 (4'S,2E)-3-methyl-5-(2',2',5',5'-tetramethyl-1',3'-dioxolan-4'-yl)-2-penten-1-ol 
• 56752-50-2 Acetic acid (S)-2,2,6-trimethyl-6-vinyl-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

Verbena x hybrida flower volatiles attractive to Western flower thrips, Frankliniella occidentalis

Western flower thrips (WFT) are attracted to three flowering verbena cultivars. The volatile components of these cultivars contain different enantiomers of linalool oxide which ahve been synthesised and one shown to be attractive to WFT.

Microbiological Transformations. 19. Asymmetric Dihydroxylation of the Remote Double Bond of Geraniol: A Unique Stereochemical Control Allowing Easy Access to Both Enantiomers of Geraniol-6,7-diol

The microbiological oxygenation of the geraniol N-phenylcarbamate 1 by Aspergillus niger is described, which leads regiospecifically to a formal dihydroxylation of its C(6)=C(7) double bond.By use of different pH values of the incubation medium, it is pos