Palladium-catalysed synthesis of 1-isoindolecarboxylic acid esters and sequential Diels-Alder reactions: access to bridged- and fused-ring heterocycles

被引：26

作者：

Sole, Daniel ^{[1
]}

Serrano, Olga

机构：

[1] Univ Barcelona, Lab Quim Organ, Fac Farm, E-08028 Barcelona, Spain

来源：

ORGANIC & BIOMOLECULAR CHEMISTRY | 2009年 / 7卷 / 17期

关键词：

INTRAMOLECULAR ALPHA-ARYLATION; ARYL HALIDES; ENOLATE ARYLATION; ISOINDOLE; DERIVATIVES; NAPHTHALENES; RESEARCHES; CHEMISTRY; KETONES;

D O I：

10.1039/b909701e

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The Pd-catalysed intramolecular alpha-arylation of alpha-amino acid esters provides a useful methodology for the synthesis of substituted isoindole derivatives, which have been used in Diels-Alder reactions to access diverse skeletal frameworks.

引用

页码：3382 / 3384

页数：3

共 2 条

[1] Diastereoselective Synthesis of Coumarin-Based Fused Heterocycles via Intramolecular Diels-Alder and 1,3-Dipolar Cycloaddition Reactions
Alizadeh, Abdolali
Farajpour, Behnaz
Amir Ashjaee Asalemi, Kaveh
Taghipour, Sajad
CHEMISTRYSELECT, 2020, 5 (31): : 9834 - 9838
[2] Synthesis of azepane-fused pyrano[3,2-b]indoles by Lewis acid-catalysed oxa Diels-Alder reactions
Banda, Saikumar
Villinger, Alexander
Brasholz, Malte
ORGANIC & BIOMOLECULAR CHEMISTRY, 2023, 21 (21) : 4379 - 4381

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