A catalytic enantioselective tandem allylation strategy for rapid terpene construction: application to the synthesis of pumilaside aglycon.

A catalytic enantioselective tandem allylation strategy for rapid terpene construction: application to the synthesis of pumilaside aglycon.
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DOI:
10.1021/ja400506j
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发表时间:
2013-02-20
影响因子:
15
通讯作者:
Morken, James P.
Morken, James P.
中科院分区:
化学1区
文献类型:
--
作者:
Ferris, Grace E.;Hong, Kai;Roundtree, Ian A.;Morken, James P.

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Catalytic enantioselective 1,2-diboration of 1,3-dienes followed by cascade allylborations with dicarbonyls provides rapid entry into carbocyclic reaction products. The stereochemical course of this reaction was studied along with its application in the synthesis of pumilaside aglycon.
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