Synthetic Studies toward the Hamigerans with a 6-7-5 Tricyclic Core.
Synthetic Studies toward the Hamigerans with a 6-7-5 Tricyclic Core.
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DOI:
10.1021/acs.orglett.0c01253
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发表时间:
2020-06-05
期刊:
影响因子:
5.2
通讯作者:
Dai M
中科院分区:
文献类型:
--
作者:
Jiang B;Dai M
An approach towards the 6-7-5 tricyclic carbon skeleton of the hamigeran natural products was developed. The key steps include a benzyne-β-ketoester annulative ring expansion to form the 7-membered ring, a Nazarov reaction to form the 5-membered ring, a Ni-catalyzed conjugate methyl addition or a Corey-Chaykovsky reaction to install the all-carbon quaternary center, and a Suzuki cross coupling followed by reduction to introduce the isopropyl group.
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