2002
DOI: 10.1016/s1381-1177(02)00015-2
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Baker’s yeast mediated preparation of (10-alkyl-10H-phenothiazin-3-yl)methanols

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Cited by 19 publications
(4 citation statements)
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“…Over the assay time frame phenothiazine sulfoxide was the major isolated metabolite (Figure 2-10). These results are similar to bioconversions of phenothiazine with the yeast C. elegans 78 , B. bassiana 111 , and the functional group conversions identified in the oxidation of phenothiazine drugs 79,83,84,116…”
Section: Metabolite Characterizationsupporting
confidence: 73%
See 1 more Smart Citation
“…Over the assay time frame phenothiazine sulfoxide was the major isolated metabolite (Figure 2-10). These results are similar to bioconversions of phenothiazine with the yeast C. elegans 78 , B. bassiana 111 , and the functional group conversions identified in the oxidation of phenothiazine drugs 79,83,84,116…”
Section: Metabolite Characterizationsupporting
confidence: 73%
“…, its metabolism has been thoroughly studied in mammals 82 . The oxidation of phenothiazine and substituted phenothiazine drugs has been studied in the lower fungi C. elegans 78 and endophytic fungi 79,83,84 . Thiophenes are building blocks in many agrochemicals, pharmaceuticals (lornoxicam), and electrically conductive polymers 86 .…”
Section: Sulfoxide Importancementioning
confidence: 99%
“…The synthesis of aldehydes 1a-e was previously described. 19 All solvents were purified and dried by standard methods as required. 20 Amberlite IRA 904 was purchased from Acros and was conditioned as previously described.…”
Section: Methodsmentioning
confidence: 99%
“…9 During the work-up and purification procedures the instability of N-substituted phenothiazin-3-yl-ethanols rac2a-d was observed. While at room temperature and neutral pH they are relatively stable, slowly decomposing compounds, at higher temperature or at lower pH the easy water elimination could be the explanation for the high instability of rac-2a-d.…”
Section: Chemical Synthesismentioning
confidence: 99%