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A total synthesis of (±)-1-desoxyhypnophilin: using ring closing metathesis for the construction of cyclic enones

✍ Scribed by David C Harrowven; Matthew C Lucas; Peter D Howes


Publisher
Elsevier Science
Year
2000
Tongue
French
Weight
73 KB
Volume
41
Category
Article
ISSN
0040-4039

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✦ Synopsis


The paper describes the first total synthesis of (±)-1-desoxyhypnophilin, a linear triquinane isolated from the East African mushroom Lentinus crinitus which displays promising antimicrobial activity. The key strategic feature is a new cyclopentannulation method for appending cycloalkenones onto ketones involving sequential use of a ring closing metathesis reaction with a tertiary allylic alcohol and a PCC induced oxidative rearrangement.


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ChemInform Abstract: A Total Synthesis o
✍ David C. Harrowven; Matthew C. Lucas; Peter D. Howes 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

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