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Regioselectivity inversion tuned by iron(iii) salts in palladium-catalyzed carbonylations†
Chemical Communications ( IF 4.3 ) Pub Date : 2018-03-22 00:00:00 , DOI: 10.1039/c8cc01190g
Zijun Huang 1, 2, 3, 4, 5 , Yazhe Cheng 1, 2, 3, 4, 5 , Xipeng Chen 1, 2, 3, 4, 5 , Hui-Fang Wang 6, 7, 8, 9, 10 , Chen-Xia Du 11, 12, 13, 14 , Yuehui Li 1, 2, 3, 4, 5
Affiliation  

Impactful regioselectivity control is crucial for cost-effective chemical synthesis. By using cheap and abundant iron(III) salts, the hydroxycarbonylations of both aromatic and aliphatic alkenes were significantly enhanced in both reactivity and selectivity (iso/n or n/iso up to >99 : 1). Moreover, Pd-catalyzed carbonylation selectivity can be switched from branched to linear by using different Fe(III) salts. In addition, similar results were obtained for the carbonylation of secondary alcohols.

中文翻译:

铁(iii)盐在钯催化的羰基化反应中调节的区域选择性反演

有效的区域选择性控制对于经济高效的化学合成至关重要。通过使用廉价而丰富的铁(III)盐,芳族和脂族烯烃的羟羰基化反应性和选择性都得到了显着提高(iso / nn / iso高达> 99:1)。此外,可以通过使用不同的Fe(III)盐将Pd催化的羰基化选择性从支链切换为线性。另外,对于仲醇的羰基化获得了相似的结果。
更新日期:2018-03-22
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