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- W1964867985 abstract "An intramolecular Diels-Alder (IMDA)-tandem metathesis strategy is used to access a vinyl triquinane skeleton and a formal synthesis of (±)-Δ9(¹²)-capnellene is realized. A variety of strategies have been applied to the synthesis of similar terpenoids (see Review below) and this sequence is an interesting addition. The authors also present a discussion of two possible metathesis sequences: ring-opening-ring-closing metathesis (ROM-RCM) versus ring-closing-ring-opening-cross-metathesis (RCM-ROM-CM, pictured). Evidence supporting the latter proposal is disclosed." @default.
- W1964867985 created "2016-06-24" @default.
- W1964867985 date "2010-06-22" @default.
- W1964867985 modified "2023-09-26" @default.
- W1964867985 title "Diastereoselective Domino Synthesis of Triquinanes" @default.
- W1964867985 doi "https://doi.org/10.1055/s-0029-1220080" @default.
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