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- W1574752416 endingPage "1374" @default.
- W1574752416 startingPage "1365" @default.
- W1574752416 abstract "An efficient, mild, and highly diastereoselective strategy for the synthesis of trans-2,6-disubstituted-5-methyl-3,6-dihydropyran ring systems has been developed starting from δ-hydroxy α-methyl α,β-unsaturated aldehydes and allyltrimethylsilane in the presence of a catalytic amount of ZnBr2 in a highly diastereoselective manner with excellent yield. The versatility of the above method was also demonstrated for the construction of the bicyclic core present in penostatin B in a concise and highly stereoselective manner." @default.
- W1574752416 created "2016-06-24" @default.
- W1574752416 creator A5001690439 @default.
- W1574752416 creator A5035230211 @default.
- W1574752416 creator A5036517273 @default.
- W1574752416 date "2015-01-28" @default.
- W1574752416 modified "2023-10-16" @default.
- W1574752416 title "Highly Stereocontrolled Synthesis of <i>trans</i>-2,6-Disubstituted-5-methyl-3,6-dihydropyrans: Stereoselective Synthesis of the Bicyclic Core of Penostatin B" @default.
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- W1574752416 doi "https://doi.org/10.1021/jo502101u" @default.
- W1574752416 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25585160" @default.
- W1574752416 hasPublicationYear "2015" @default.
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