Preparation and structure of di-exo-condensed norbornane heterocycles

Ferenc Miklós, A. Hetényi, P. Sohár, G. Stájer

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Cyclization of di-exo-aroylnorbornanecarboxylic acid with bidentate nucleophiles (hydrazine, o-phenylenediamine, o-aminophenol, alkylenediamines, and amino alcohols) yielded heterotri-, tetra-, and pentacycles. Their structures were established by means of NMR spectroscopy, with the application of HMQC, HMBC, DEPT, DIFFNOE, and COSY methods.

Original languageEnglish
Pages (from-to)839-847
Number of pages9
JournalMonatshefte fur Chemie
Volume135
Issue number7
Publication statusPublished - Jul 2004

Fingerprint

hydrazine
Norbornanes
Amino Alcohols
Nucleophiles
Cyclization
Nuclear magnetic resonance spectroscopy
Acids
vitamin B 12 factor III
2-aminophenol
1,2-diaminobenzene

Keywords

  • Bicyclo[2.2.1]heptane derivatives
  • Cyclizations
  • Heterocycles
  • Isoindolones

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Preparation and structure of di-exo-condensed norbornane heterocycles. / Miklós, Ferenc; Hetényi, A.; Sohár, P.; Stájer, G.

In: Monatshefte fur Chemie, Vol. 135, No. 7, 07.2004, p. 839-847.

Research output: Contribution to journalArticle

@article{a38b9187927e42e1b3353d87715669b9,
title = "Preparation and structure of di-exo-condensed norbornane heterocycles",
abstract = "Cyclization of di-exo-aroylnorbornanecarboxylic acid with bidentate nucleophiles (hydrazine, o-phenylenediamine, o-aminophenol, alkylenediamines, and amino alcohols) yielded heterotri-, tetra-, and pentacycles. Their structures were established by means of NMR spectroscopy, with the application of HMQC, HMBC, DEPT, DIFFNOE, and COSY methods.",
keywords = "Bicyclo[2.2.1]heptane derivatives, Cyclizations, Heterocycles, Isoindolones",
author = "Ferenc Mikl{\'o}s and A. Het{\'e}nyi and P. Soh{\'a}r and G. St{\'a}jer",
year = "2004",
month = "7",
language = "English",
volume = "135",
pages = "839--847",
journal = "Monatshefte fur Chemie",
issn = "0026-9247",
publisher = "Springer Wien",
number = "7",

}

TY - JOUR

T1 - Preparation and structure of di-exo-condensed norbornane heterocycles

AU - Miklós, Ferenc

AU - Hetényi, A.

AU - Sohár, P.

AU - Stájer, G.

PY - 2004/7

Y1 - 2004/7

N2 - Cyclization of di-exo-aroylnorbornanecarboxylic acid with bidentate nucleophiles (hydrazine, o-phenylenediamine, o-aminophenol, alkylenediamines, and amino alcohols) yielded heterotri-, tetra-, and pentacycles. Their structures were established by means of NMR spectroscopy, with the application of HMQC, HMBC, DEPT, DIFFNOE, and COSY methods.

AB - Cyclization of di-exo-aroylnorbornanecarboxylic acid with bidentate nucleophiles (hydrazine, o-phenylenediamine, o-aminophenol, alkylenediamines, and amino alcohols) yielded heterotri-, tetra-, and pentacycles. Their structures were established by means of NMR spectroscopy, with the application of HMQC, HMBC, DEPT, DIFFNOE, and COSY methods.

KW - Bicyclo[2.2.1]heptane derivatives

KW - Cyclizations

KW - Heterocycles

KW - Isoindolones

UR - http://www.scopus.com/inward/record.url?scp=3242696245&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=3242696245&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:3242696245

VL - 135

SP - 839

EP - 847

JO - Monatshefte fur Chemie

JF - Monatshefte fur Chemie

SN - 0026-9247

IS - 7

ER -