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• W2139610488 abstract "An efficient route using nitroalkane synthon 3a and 3b for the synthesis of optically pure R-(+)-trans whisky lactone, (+)-9 and R-(+)-eldanolide, (+)-10 is described. In a key step, bakers' yeast reduction is employed to get the required chirality." @default.
• W2139610488 created "2016-06-24" @default.
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• W2139610488 date "1993-03-01" @default.
• W2139610488 modified "2023-10-12" @default.
• W2139610488 title "Nitro alkanes in organic synthesis: An efficient stereoselective synthesis of (+)-trans whisky lactone and (+)-eldanolide from nitro alkane synthons and using bakers' yeast reduction as the key step" @default.
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• W2139610488 doi "https://doi.org/10.1016/s0040-4020(01)80369-0" @default.
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