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Page 1
Bacterial metabolism of 2,6-xylenol.
Ewers J, Rubio MA, Knackmuss HJ, Freier-Schröder D. Ewers J, et al. Appl Environ Microbiol. 1989 Nov;55(11):2904-8. doi: 10.1128/aem.55.11.2904-2908.1989. Appl Environ Microbiol. 1989. PMID: 16348052 Free PMC article.
Intact cells of Mycobacterium strain DM1 grown with 2,6-xylenol cooxidized 2,4,6-trimethylphenol to 2,4,6-trimethylresorcinol. 4-Chloro-3,5-dimethylphenol prevents 2,6-xylenol from being totally degraded; it was quantitatively converted t …
Intact cells of Mycobacterium strain DM1 grown with 2,6-xylenol cooxidized 2,4,6-trimethylphenol to 2,4,6-trimethylreso …
Organocatalytic Enantioselective Synthesis of Bicyclo[2.2.2]octenones via Oxaziridinium Catalysed ortho-Hydroxylative Phenol Dearomatization.
D'Arcy TD, Elsegood MRJ, Buckley BR. D'Arcy TD, et al. Angew Chem Int Ed Engl. 2022 Jul 25;61(30):e202205278. doi: 10.1002/anie.202205278. Epub 2022 Jun 10. Angew Chem Int Ed Engl. 2022. PMID: 35543699 Free PMC article.
This approach was applied to the highly enantioselective synthesis of (+)-biscarvacrol (99 : 1 e.r.) and (-)-bis(2,6-xylenol) (94 : 6 e.r.). The practicality of our conditions was demonstrated at gram-scale, using an amine precatalyst, accessible in a single …
This approach was applied to the highly enantioselective synthesis of (+)-biscarvacrol (99 : 1 e.r.) and (-)-bis(2,6-xyleno
Carbon Dioxide Solubility in Nonionic Deep Eutectic Solvents Containing Phenolic Alcohols.
Alhadid A, Safarov J, Mokrushina L, Müller K, Minceva M. Alhadid A, et al. Front Chem. 2022 Mar 22;10:864663. doi: 10.3389/fchem.2022.864663. eCollection 2022. Front Chem. 2022. PMID: 35392423 Free PMC article.
CO(2) solubility was experimentally determined in two different DES, namely, L-menthol/thymol in 1:2 molar ratio and thymol/2,6-xylenol in 1:1 molar ratio, at various temperatures and pressures. ...
CO(2) solubility was experimentally determined in two different DES, namely, L-menthol/thymol in 1:2 molar ratio and thymol/2,6
56 results