Preparation of some nitrogen-containing 2,5-dialkoxystyrene derivatives

被引：0

作者：

Borja, Guadalupe ^{[1
]}

Pleixats, Roser ^{[1
]}

Shafir, Alexandr ^{[1
]}

Parella, Teodor ^{[2
]}

机构：

[1] Univ Autonoma Barcelona, Dept Chem, E-08193 Barcelona, Spain

[2] Univ Autonoma Barcelona, Serv Ressonancia Magnet Nucl, E-08193 Barcelona, Spain

来源：

ARKIVOC | 2010年

关键词：

Styrene derivatives; triazine derivatives; Wittig reaction; OLEFIN METATHESIS CATALYSTS; GRUBBS RUTHENIUM CARBENES; CATIONIC-POLYMERIZATION; EFFICIENT; HYDROGEN; STEP;

D O I：

10.3998/ark.5550190.0011.315

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The synthesis of 2,5-dialkoxystyrene derivatives starting from 2,5-dihydroxybenzaldehyde is described. The key steps in the synthesis are the alkylation of the phenolic hydroxyl groups and subsequent Wittig olefination of the aldehyde moiety. The ether side-chains of the products display several nitrogen-containing functional groups, including phthalimido, tert-butoxycarbonylamino, cyano and aminotriazines.

引用

页码：169 / 180

页数：12

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