Long-chain substituted tetracyanoquinodimethanes: A convenient synthetic approach

M. Utinans; V. Khodorkovsky; O. Neilands

doi:10.1081/SCC-100103524

Long-chain substituted tetracyanoquinodimethanes: A convenient synthetic approach

M. Utinans
, V. Khodorkovsky
, O. Neilands

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

Abstract

2-Alkylcyclohexane-1,4-diones, key precursors of TCNQ derivatives, have been synthesized by modified Birch reduction of 2,5-dimethoxybenzoic acid by Li and Et₂NH in an ultrasonic bath and subsequent alkylation.

Original language	English
Pages (from-to)	971-974
Number of pages	4
Journal	Synthetic Communications
Volume	31
Issue number	7
DOIs	https://doi.org/10.1081/SCC-100103524
State	Published - 1 Jan 2001
Externally published	Yes

ASJC Scopus subject areas

Organic Chemistry

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10.1081/SCC-100103524

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@article{9e9bf35d8ae14b7c92b0dec700aef96b,

title = "Long-chain substituted tetracyanoquinodimethanes: A convenient synthetic approach",

abstract = "2-Alkylcyclohexane-1,4-diones, key precursors of TCNQ derivatives, have been synthesized by modified Birch reduction of 2,5-dimethoxybenzoic acid by Li and Et2NH in an ultrasonic bath and subsequent alkylation.",

author = "M. Utinans and V. Khodorkovsky and O. Neilands",

year = "2001",

month = jan,

day = "1",

doi = "10.1081/SCC-100103524",

language = "English",

volume = "31",

pages = "971--974",

journal = "Synthetic Communications",

issn = "0039-7911",

publisher = "Taylor and Francis Ltd.",

number = "7",

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TY - JOUR

T1 - Long-chain substituted tetracyanoquinodimethanes

T2 - A convenient synthetic approach

AU - Utinans, M.

AU - Khodorkovsky, V.

AU - Neilands, O.

PY - 2001/1/1

Y1 - 2001/1/1

N2 - 2-Alkylcyclohexane-1,4-diones, key precursors of TCNQ derivatives, have been synthesized by modified Birch reduction of 2,5-dimethoxybenzoic acid by Li and Et2NH in an ultrasonic bath and subsequent alkylation.

AB - 2-Alkylcyclohexane-1,4-diones, key precursors of TCNQ derivatives, have been synthesized by modified Birch reduction of 2,5-dimethoxybenzoic acid by Li and Et2NH in an ultrasonic bath and subsequent alkylation.

UR - https://www.scopus.com/pages/publications/0034995681

U2 - 10.1081/SCC-100103524

DO - 10.1081/SCC-100103524

M3 - Article

AN - SCOPUS:0034995681

SN - 0039-7911

VL - 31

SP - 971

EP - 974

JO - Synthetic Communications

JF - Synthetic Communications

IS - 7

ER -

Long-chain substituted tetracyanoquinodimethanes: A convenient synthetic approach

Abstract

ASJC Scopus subject areas

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