Structure and absolute configuration of (–)-taylorione, a novel carbon skeletal sesquiterpene ketone of ent-1,10-seco-aromadendrane form, from Mylia taylorii(liverwort)
“…The structure of (+)-taylorione 365 was elucidated and its absolute conguration was determined by combination of its spectral data analysis and degradation investigation. 240 The total synthesis (+)-taylorione 365 was accomplished and reported by Kerr et al in 1996 (ref. 241) 245,246 This tricyclic sesquiterpene 375 is involved in the biosynthesis of neopentalenolactone antibiotic.…”
Section: Sesquiterpenesmentioning
confidence: 99%
“…The structure of (+)-taylorione 365 was elucidated and its absolute configuration was determined by combination of its spectral data analysis and degradation investigation. 240 …”
Section: Applications Of Pauson–khand Reaction In the Total Synthesis...mentioning
The Pauson–Khand reaction (PKR) is a formal [2 + 2 + 1] cycloaddition involving an alkyne, an alkene and carbon monoxide mediated by a hexacarbonyldicobaltalkyne complex to yield cyclopentenones in a single step.
“…The structure of (+)-taylorione 365 was elucidated and its absolute conguration was determined by combination of its spectral data analysis and degradation investigation. 240 The total synthesis (+)-taylorione 365 was accomplished and reported by Kerr et al in 1996 (ref. 241) 245,246 This tricyclic sesquiterpene 375 is involved in the biosynthesis of neopentalenolactone antibiotic.…”
Section: Sesquiterpenesmentioning
confidence: 99%
“…The structure of (+)-taylorione 365 was elucidated and its absolute configuration was determined by combination of its spectral data analysis and degradation investigation. 240 …”
Section: Applications Of Pauson–khand Reaction In the Total Synthesis...mentioning
The Pauson–Khand reaction (PKR) is a formal [2 + 2 + 1] cycloaddition involving an alkyne, an alkene and carbon monoxide mediated by a hexacarbonyldicobaltalkyne complex to yield cyclopentenones in a single step.
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