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- W2078352807 abstract "The routes towards the proposed, (I), and revised, (II), structures of aspergillide B involve kinetically controlled ring-closing metathesis for the construction of the 14-membered macrocyclic ring, ester formation by employing Yamaguchi conditions, a Wacker-type oxidative cyclization with respect to creation of the C-4 stereogenic center, as well as a previously reported diastereoselective isomerization-iodocyclization strategy for the construction of the 2,6-trans-disubstituted tetrahydropyran subunit." @default.
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- W2078352807 date "2014-09-25" @default.
- W2078352807 modified "2023-09-22" @default.
- W2078352807 title "ChemInform Abstract: Total Synthesis of the Z-Isomers of the Proposed and Revised Structures of Aspergillide B via an Iodocyclization and Ring-Closing Metathesis Strategy." @default.
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- W2078352807 doi "https://doi.org/10.1002/chin.201441216" @default.
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