Synthesis of new β-carboline derivatives via 1,7-electrocyclisation of azomethine ylides

Miklós Nyerges, A. Virányi, J. Tóth, Gábor Blaskó, L. Tőke

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

A new route to the benzo[5,6]azepino[2,1-a]-β-carboline and indazolo[3,2-a]-β-carboline ring systems has been developed via the 1,7-dipolar electrocyclisation reactions of azomethine ylides derived from easily available β-carboline derivatives.

Original languageEnglish
Pages (from-to)1273-1278
Number of pages6
JournalSynthesis
Issue number8
DOIs
Publication statusPublished - Apr 19 2006

Fingerprint

Carbolines
Derivatives
azomethine

Keywords

  • Electrocyclic reactions
  • Heterocycles
  • Tandem reactions
  • Ylides

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Synthesis of new β-carboline derivatives via 1,7-electrocyclisation of azomethine ylides. / Nyerges, Miklós; Virányi, A.; Tóth, J.; Blaskó, Gábor; Tőke, L.

In: Synthesis, No. 8, 19.04.2006, p. 1273-1278.

Research output: Contribution to journalArticle

@article{5bbe057273a741cc945411a3346588f6,
title = "Synthesis of new β-carboline derivatives via 1,7-electrocyclisation of azomethine ylides",
abstract = "A new route to the benzo[5,6]azepino[2,1-a]-β-carboline and indazolo[3,2-a]-β-carboline ring systems has been developed via the 1,7-dipolar electrocyclisation reactions of azomethine ylides derived from easily available β-carboline derivatives.",
keywords = "Electrocyclic reactions, Heterocycles, Tandem reactions, Ylides",
author = "Mikl{\'o}s Nyerges and A. Vir{\'a}nyi and J. T{\'o}th and G{\'a}bor Blask{\'o} and L. Tőke",
year = "2006",
month = "4",
day = "19",
doi = "10.1055/s-2006-926400",
language = "English",
pages = "1273--1278",
journal = "Synthesis",
issn = "0039-7881",
publisher = "Georg Thieme Verlag",
number = "8",

}

TY - JOUR

T1 - Synthesis of new β-carboline derivatives via 1,7-electrocyclisation of azomethine ylides

AU - Nyerges, Miklós

AU - Virányi, A.

AU - Tóth, J.

AU - Blaskó, Gábor

AU - Tőke, L.

PY - 2006/4/19

Y1 - 2006/4/19

N2 - A new route to the benzo[5,6]azepino[2,1-a]-β-carboline and indazolo[3,2-a]-β-carboline ring systems has been developed via the 1,7-dipolar electrocyclisation reactions of azomethine ylides derived from easily available β-carboline derivatives.

AB - A new route to the benzo[5,6]azepino[2,1-a]-β-carboline and indazolo[3,2-a]-β-carboline ring systems has been developed via the 1,7-dipolar electrocyclisation reactions of azomethine ylides derived from easily available β-carboline derivatives.

KW - Electrocyclic reactions

KW - Heterocycles

KW - Tandem reactions

KW - Ylides

UR - http://www.scopus.com/inward/record.url?scp=33646261672&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=33646261672&partnerID=8YFLogxK

U2 - 10.1055/s-2006-926400

DO - 10.1055/s-2006-926400

M3 - Article

SP - 1273

EP - 1278

JO - Synthesis

JF - Synthesis

SN - 0039-7881

IS - 8

ER -