Asymmetric total synthesis of (+)-fostriecin.

Asymmetric total synthesis of (+)-fostriecin.
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( )-磷霉素的不对称全合成。

DOI:
10.1021/ol025537r
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发表时间:
2002
期刊:
影响因子:
5.2
通讯作者:
Falck,JR
Falck,JR
中科院分区:
化学1区
文献类型:
--
作者:
Reddy,YKrishna;Falck,JR

文献摘要

被引文献

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The title compound, a potent protein phosphatase inhibitor and anticancer agent, was prepared by an efficient, multiconvergent asymmetric synthesis. Key transformations include a ring forming olefin metathesis leading to the α,β-unsaturated lactone and creation of the triene moiety via Suzuki cross-coupling.