Palladium-catalyzed asymmetric allylic C-H alkylation of 1,4-dienes and glycine Schiff bases

Palladium-catalyzed asymmetric allylic C-H alkylation of 1,4-dienes and glycine Schiff bases
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钯催化 1,4-二烯和甘氨酸席夫碱的不对称烯丙基 C-H 烷基化

DOI:
10.1007/s11426-019-9687-1
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发表时间:
2020-03
影响因子:
9.6
通讯作者:
Gong Liu-Zhu
Gong Liu-Zhu
中科院分区:
化学1区
文献类型:
--
作者:
Wang Tian-Ci;Wang Pu-Sheng;Gong Liu-Zhu

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A highly regio- and enantioselective allylic C-H alkylation of 1,4-dienes with glycine Schiff bases has been established by chiral palladium-phosphoramidite catalysis. This reaction can proceed under mild conditions and tolerate a wide scope of 1,4-dienes, delivering structurally diverse chiral β-branched a-amino acid surrogates in moderate to high yields and with high levels of regio-, Z / E -, diastereo- and enantioselectivities.
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