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

Guadalupe Borja; Roser Pleixats; Alexandr Shafir; Teodor Parella

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

Guadalupe Borja, Roser Pleixats, Alexandr Shafir, Teodor Parella

Department of Chemistry

Research output: Contribution to journal › Article › Research › peer-review

Abstract

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, tertbutoxycarbonylamino, cyano and aminotriazines.

Original language	English
Pages (from-to)	169-180
Journal	Arkivoc
Volume	2010
Issue number	3
Publication status	Published - 17 Jun 2010

Keywords

Styrene derivatives
Triazine derivatives
Wittig reaction

Cite this

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title = "Preparation of some nitrogen-containing 2,5-dialkoxystyrene derivatives",

abstract = "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, tertbutoxycarbonylamino, cyano and aminotriazines.",

keywords = "Styrene derivatives, Triazine derivatives, Wittig reaction",

author = "Guadalupe Borja and Roser Pleixats and Alexandr Shafir and Teodor Parella",

year = "2010",

month = jun,

day = "17",

language = "English",

volume = "2010",

pages = "169--180",

journal = "Arkivoc",

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TY - JOUR

T1 - Preparation of some nitrogen-containing 2,5-dialkoxystyrene derivatives

AU - Borja, Guadalupe

AU - Pleixats, Roser

AU - Shafir, Alexandr

AU - Parella, Teodor

PY - 2010/6/17

Y1 - 2010/6/17

N2 - 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, tertbutoxycarbonylamino, cyano and aminotriazines.

AB - 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, tertbutoxycarbonylamino, cyano and aminotriazines.

KW - Styrene derivatives

KW - Triazine derivatives

KW - Wittig reaction

M3 - Article

SN - 1551-7004

VL - 2010

SP - 169

EP - 180

JO - Arkivoc

JF - Arkivoc

IS - 3

ER -

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

Abstract

Keywords

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