1999
DOI: 10.1002/(sici)1099-0690(199910)1999:10<2533::aid-ejoc2533>3.0.co;2-o
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EPC Syntheses of Trifluorocitronellol and of Hexafluoropyrenophorin – A Comparison of Their Physiological Properties with the Nonfluorinated Analogs
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Cited by 26 publications
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“…In a second approach (cf. B in Scheme 8), the aldol addition of the oxazolidinone derivatives III with aldehydes IV (PG' Tr [107]; PG' Ts [106]), followed by deoxygenation under Barton ± McCombie conditions [67] [108] [ 109], resulted in the isolation of degradation products caused by retro-aldol reactions, occurring during the deoxygenation step. Thus, the amidomethylation reaction via Ti-enolates was attempted (cf.…”
mentioning
confidence: 99%
“…In a second approach (cf. B in Scheme 8), the aldol addition of the oxazolidinone derivatives III with aldehydes IV (PG' Tr [107]; PG' Ts [106]), followed by deoxygenation under Barton ± McCombie conditions [67] [108] [ 109], resulted in the isolation of degradation products caused by retro-aldol reactions, occurring during the deoxygenation step. Thus, the amidomethylation reaction via Ti-enolates was attempted (cf.…”
mentioning
confidence: 99%
