Formation of 2-arylnaphthalenes from N-tosylated phenylalanine derivatives

被引：13

作者：

Seong, MR ^{[1
]}

Song, HN ^{[1
]}

Kim, JN ^{[1
]}

机构：

[1] Chonnam Natl Univ, Dept Chem, Kwangju 500757, South Korea

来源：

TETRAHEDRON LETTERS | 1998年 / 39卷 / 39期

关键词：

2-arylnaphthalenes; Friedel-Crafts reaction; N-tosylated phenylalanine;

D O I：

10.1016/S0040-4039(98)01507-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

N-Tosylated phenylalanine derivatives in benzene in the presence of sulfuric acid afforded 2-arylnaphthalene derivatives in moderate yields. The reaction might proceed via the corresponding decarbonylated N-tosylimine derivatives. Aldol type reaction of N-tosylimines followed by intramolecular Friedel-Crafts reaction and elimination of p-toluenesulfonamide gave 2-arylnaphthalenes. (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：7101 / 7104

页数：4

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