Results 111 to 120 of about 33,103 (197)

The asymmetric synthesis of (+)-sitophilure, the natural form of the aggregation pheromone of Sitophilus oryzae L. and Sitophilus zeamais M.

open access: yesJournal of the Brazilian Chemical Society, 1999
The asymmetric synthesis of (+)-sitophilure, the aggregation pheromone of Sitophilus oryzae L. and Sitophilus zeamais M., was carried out in 12 steps, 18% overall yield and 82% enantiomeric excess from the enzymatic reduction of methyl 3-oxopentanoate ...
Pilli Ronaldo A., Riatto Valéria B.
doaj  

Chiral thiols. Synthesis and enantiomeric excess determination

open access: yes, 1987
Chiral thiols are a class of chira compounds, which is gaining mone and nore attention the last decenniun. Especially α-mercaptocarboxylic acids are frequently found as a structunal unit in (biologically) important products. As a consequence, many synthetic analoga or derivatives of these natural products, but also other organosulfur compounds, have ...
openaire   +1 more source

High Enantiomeric Excess In-Loop Synthesis of d-[methyl-11C]Methionine for Use as a Diagnostic Positron Emission Tomography Radiotracer in Bacterial Infection. [PDF]

open access: yesACS Infect Dis, 2020
Stewart MN   +13 more
europepmc   +1 more source

Enantiomeric Excess Bupivacaine in a Lavender Oil NLC Tested in a Melanoma Model: Prolonged Release and Anticancer Effect. [PDF]

open access: yesMol Pharm
Geronimo G   +10 more
europepmc   +1 more source

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