trans-3-Aryl-4-nitro-pyrrolidines via 1,3-dipolar cycloaddition of nonstabilized azomethine ylide to ß-nitro styrenes

Miklós Nyerges, László Balázs, István Kádas, I. Bitter, István Kövesdi, L. Tőke

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

Various β-nitro styrenes undergo 1,3 dipolar cycloaddition with the azomethine ylide derived from sarcosine and paraformaldehyde to give 3-aryl-4-nitro-pyrrolidines in good yield.

Original languageEnglish
Pages (from-to)6783-6788
Number of pages6
JournalTetrahedron
Volume51
Issue number24
DOIs
Publication statusPublished - Jun 12 1995

Fingerprint

Styrenes
Pyrrolidines
Sarcosine
Cycloaddition
Cycloaddition Reaction
paraform
azomethine

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

trans-3-Aryl-4-nitro-pyrrolidines via 1,3-dipolar cycloaddition of nonstabilized azomethine ylide to ß-nitro styrenes. / Nyerges, Miklós; Balázs, László; Kádas, István; Bitter, I.; Kövesdi, István; Tőke, L.

In: Tetrahedron, Vol. 51, No. 24, 12.06.1995, p. 6783-6788.

Research output: Contribution to journalArticle

Nyerges, Miklós ; Balázs, László ; Kádas, István ; Bitter, I. ; Kövesdi, István ; Tőke, L. / trans-3-Aryl-4-nitro-pyrrolidines via 1,3-dipolar cycloaddition of nonstabilized azomethine ylide to ß-nitro styrenes. In: Tetrahedron. 1995 ; Vol. 51, No. 24. pp. 6783-6788.
@article{bf841f09aa0840cdba19248f13335ead,
title = "trans-3-Aryl-4-nitro-pyrrolidines via 1,3-dipolar cycloaddition of nonstabilized azomethine ylide to {\ss}-nitro styrenes",
abstract = "Various β-nitro styrenes undergo 1,3 dipolar cycloaddition with the azomethine ylide derived from sarcosine and paraformaldehyde to give 3-aryl-4-nitro-pyrrolidines in good yield.",
author = "Mikl{\'o}s Nyerges and L{\'a}szl{\'o} Bal{\'a}zs and Istv{\'a}n K{\'a}das and I. Bitter and Istv{\'a}n K{\"o}vesdi and L. Tőke",
year = "1995",
month = "6",
day = "12",
doi = "10.1016/0040-4020(95)00311-U",
language = "English",
volume = "51",
pages = "6783--6788",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Elsevier Limited",
number = "24",

}

TY - JOUR

T1 - trans-3-Aryl-4-nitro-pyrrolidines via 1,3-dipolar cycloaddition of nonstabilized azomethine ylide to ß-nitro styrenes

AU - Nyerges, Miklós

AU - Balázs, László

AU - Kádas, István

AU - Bitter, I.

AU - Kövesdi, István

AU - Tőke, L.

PY - 1995/6/12

Y1 - 1995/6/12

N2 - Various β-nitro styrenes undergo 1,3 dipolar cycloaddition with the azomethine ylide derived from sarcosine and paraformaldehyde to give 3-aryl-4-nitro-pyrrolidines in good yield.

AB - Various β-nitro styrenes undergo 1,3 dipolar cycloaddition with the azomethine ylide derived from sarcosine and paraformaldehyde to give 3-aryl-4-nitro-pyrrolidines in good yield.

UR - http://www.scopus.com/inward/record.url?scp=0029020883&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0029020883&partnerID=8YFLogxK

U2 - 10.1016/0040-4020(95)00311-U

DO - 10.1016/0040-4020(95)00311-U

M3 - Article

AN - SCOPUS:0029020883

VL - 51

SP - 6783

EP - 6788

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 24

ER -