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|Title:||Enantiospecific syntheses of oxacyclodecanes from carvone via mild Lewis acid mediated etherifcation|
|Keywords:||(R)-Carvone;Terpenes;Cyclic ethers;Lewis acid;Etherification|
|Abstract:||An efficient enantiospecific syntheses of oxatri-/tetra-cyclodecanes have been accomplished starting from (R)-carvone. A mild Lewis acid (BF3×OEt2) mediated intramolecular etherification is used as the key step. Structurally aesthetic tri- and tetracyclic ethers have been synthesized.|
|Appears in Collections:||IJC-B Vol.58B(03) [March 2019]|
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