Journal
ORGANIC LETTERS
Volume 18, Issue 10, Pages 2399-2402Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b00883
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Funding
- JSPS KAKENHI [15K14718]
- Grants-in-Aid for Scientific Research [15K14718] Funding Source: KAKEN
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An expeditious enantioselective total synthesis of amphirionin-4, a remarkably potent promoter of the proliferation of ST-2 cells, has been achieved from (+/-)-(E)-1,4-hexadien-3-ol by an 8-pot sequence that features the Sharpless kinetic resolution, iodoetherification, and the CBS reduction to install the stereocenters, utilization of four one pot transformations to streamline the synthetic process, and the Stille coupling reaction at nearly the center of the target molecule to complete the total synthesis.
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