Synthesis of 1,4-diaryl-2-naphthoates based on site-selective Suzuki-Miyaura reactions

被引：17

作者：

Abid, Obaid-ur-Rahman ^{[1
,2
]}

Ibad, Muhammad Farooq ^{[1
]}

Nawaz, Muhammad ^{[1
]}

Ali, Asad ^{[1
]}

Sher, Muhammad ^{[3
]}

Rama, Nasim Hasan ^{[2
]}

Villinger, Alexander ^{[1
]}

Langer, Peter ^{[1
,4
]}

机构：

[1] Univ Rostock, Inst Chem, D-18059 Rostock, Germany

[2] Quaid i Azam Univ, Dept Chem, Islamabad, Pakistan

[3] Allama Iqbal Open Univ, Dept Chem, Islamabad, Pakistan

[4] Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany

来源：

TETRAHEDRON LETTERS | 2010年 / 51卷 / 12期

关键词：

CROSS-COUPLING REACTIONS; GAS-ADSORPTION PROFILE; ESTERS;

D O I：

10.1016/j.tetlet.2010.01.038

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The palladium(0)-catalyzed Suzuki cross-coupling reaction of the bis(triflates) of phenyl 1,4-dihydroxy-2-naphthoate afforded various 1,4-diaryl-2-naphthoates. The reactions proceeded with very good site-selectivity. Due to electronic reasons, the first attack occurred at the sterically more hindered position C-1. (C) 2010 Elsevier Ltd. All rights reserved.

引用

页码：1541 / 1544

页数：4

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