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- W2337291225 abstract "A stereoselective synthesis of 14-membered macrolide hamigeromycin E (6) has been studied by employing ortho-lithiated formylation, Barbier allylation, Julia–Kocienski olefination, Mitsunobu esterification, and ring-closing metathesis (RCM) reactions. The final RCM reaction did not provide the target molecule. This study has prompted us to synthesize a stereoisomer of zeaenol and accomplish the total synthesis with the above protocols." @default.
- W2337291225 created "2016-06-24" @default.
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- W2337291225 date "2016-06-01" @default.
- W2337291225 modified "2023-09-24" @default.
- W2337291225 title "Carbohydrate-Based Studies Toward the Synthesis of Hamigeromycin E: A Stereoselective Total Synthesis of an Isomer of Zeaenol" @default.
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- W2337291225 doi "https://doi.org/10.1002/hlca.201500267" @default.
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