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Structure · dataset · 2026

The Convergent Synthetic Efforts toward Knightol and a Simplified Analog

Listed in ZivaHub and Deakin Research Online and DMU Figshare — shown once because both records carry DOI 10.1021/acs.joc.6c01838.s001

We report our efforts toward the convergent total synthesis of the cembranoid diterpene (−)-knightol, a marine natural product reported to exhibit antibiofilm activity against <i>Staphylococcus aureus</i>, and a rationally designed aryl analog, <i>m</i>knightol.

Description

Our strategy was guided by a two-phase approach involving construction of the macrocyclic framework, followed by selective epoxidation and further diversification.

Both targets were designed to arise from common western fragment building blocks and an eastern fragment accessible on a gram scale. A scalable cross-electrophile coupling provided efficient access to an advanced intermediate en route to the cyclophane and enabled evaluation of key late-stage transformations.

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Where it is published

Catalogue records · 1

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Provenance · 3 source records, 23 field assertions
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ZivaHuboai:figshare.com:article/3403211313 d agoJSON v1
Deakin Research Onlineoai:figshare.com:article/3403211313 d agoJSON v1
DMU Figshareoai:figshare.com:article/3403211313 d agoJSON v1
FieldAssertionExtractorEvidence
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