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Short access to 4-alkenylbenzonitriles: Reaction of anionic reduced forms of terephthalonitrile with alkenyl bromides Full article

Journal Synlett
ISSN: 0936-5214 , E-ISSN: 1437-2096
Output data Year: 2007, Number: 10, Pages: 1616-1618 Pages count : DOI: 10.1055/s-2007-982549
Tags reductive alkylation; terephthalonitrile dianion and radical anion; para-(omega-alkenyl)benzonitriles
Authors Panteleeva Elena V. , Haufe Guenter , Shteingarts Vitalij D.
Affiliations
1 (Данные Web of science) Univ Munster, Inst Organ Chem, D-48149 Munster, Germany
2 (Данные Web of science) Russian Acad Sci, Siberian Div, NN Vorozhtsov Inst Organ Chem, Novosibirsk 630090, Russia
3 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia

Abstract: Direct one-pot syntheses of 4-(omega-alkenyl)-benzonitriles in high yields have been achieved via the reaction of terephthalonitrile dianion with allyl or omega-alkenyl bromides in liquid ammonia.
Cite: Panteleeva E.V. , Haufe G. , Shteingarts V.D.
Short access to 4-alkenylbenzonitriles: Reaction of anionic reduced forms of terephthalonitrile with alkenyl bromides
Synlett. 2007. N10. P.1616-1618. DOI: 10.1055/s-2007-982549 WOS Scopus OpenAlex
Dates:
Published print: Jun 1, 2007
Identifiers:
Web of science: WOS:000247832200032
Scopus: 2-s2.0-34347334635
OpenAlex: W2949951610
Citing:
DB Citing
Web of science 5
Scopus 3
OpenAlex 3
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