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- W1977462999 abstract "Abstract For the first time, electrophilic cyclization and ring‐closing metathesis were used as key steps in the synthesis of a macrocyclic enediyne system, which allowed a 12‐membered dienediyne containing a thiophene‐fused ring to be obtained. The macrocycle synthesized represents a class of compounds that possess planar chirality and exists in the solid state as two enantiomers, whereas in solution the rate of interconversion is rapid as a result of unhindered switching of the double bond through the macrocycle." @default.
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- W1977462999 date "2012-09-03" @default.
- W1977462999 modified "2023-10-10" @default.
- W1977462999 title "Electrophilic Cyclization and Ring-Closing Metathesis as Key Steps in the Synthesis of a 12-Membered Cyclic Enediyne" @default.
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- W1977462999 doi "https://doi.org/10.1002/ejoc.201200881" @default.
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