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- W2951888714 abstract "A concise synthesis of the core structure of the macrolide neopeltolide was developed featuring a Prins cyclization to fashion the pyran ring. Key steps in the synthesis of aldehyde 16 were a Leighton allylation and a Feringa-Minnaard asymmetric methyl cuprate addition to an unsaturated thioester. For lactonization, a classical Yamaguchi macrolactonization was used. The longest linear sequence consists of 17 steps providing lactone 26 with an overall yield of 23%." @default.
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- W2951888714 date "2008-02-27" @default.
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- W2951888714 title "Formal Total Synthesis of Neopeltolide" @default.
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- W2951888714 doi "https://doi.org/10.1021/ol8001255" @default.
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