Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps

A tricyclic lactam is reported in a four step synthesis sequence via Beckmann rearrangement and ring-rearrangement metathesis as key steps. Here, we used a simple starting material such as dicyclopentadiene.

Detalles Bibliográficos
Autores principales: Kotha, Sambasivarao, Ravikumar, Ongolu, Majhi, Jadab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578362/
https://www.ncbi.nlm.nih.gov/pubmed/26425207
http://dx.doi.org/10.3762/bjoc.11.163
_version_ 1782391103360598016
author Kotha, Sambasivarao
Ravikumar, Ongolu
Majhi, Jadab
author_facet Kotha, Sambasivarao
Ravikumar, Ongolu
Majhi, Jadab
author_sort Kotha, Sambasivarao
collection PubMed
description A tricyclic lactam is reported in a four step synthesis sequence via Beckmann rearrangement and ring-rearrangement metathesis as key steps. Here, we used a simple starting material such as dicyclopentadiene.
format Online
Article
Text
id pubmed-4578362
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-45783622015-09-30 Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps Kotha, Sambasivarao Ravikumar, Ongolu Majhi, Jadab Beilstein J Org Chem Full Research Paper A tricyclic lactam is reported in a four step synthesis sequence via Beckmann rearrangement and ring-rearrangement metathesis as key steps. Here, we used a simple starting material such as dicyclopentadiene. Beilstein-Institut 2015-08-27 /pmc/articles/PMC4578362/ /pubmed/26425207 http://dx.doi.org/10.3762/bjoc.11.163 Text en Copyright © 2015, Kotha et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Kotha, Sambasivarao
Ravikumar, Ongolu
Majhi, Jadab
Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps
title Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps
title_full Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps
title_fullStr Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps
title_full_unstemmed Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps
title_short Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps
title_sort synthesis of a tricyclic lactam via beckmann rearrangement and ring-rearrangement metathesis as key steps
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578362/
https://www.ncbi.nlm.nih.gov/pubmed/26425207
http://dx.doi.org/10.3762/bjoc.11.163
work_keys_str_mv AT kothasambasivarao synthesisofatricycliclactamviabeckmannrearrangementandringrearrangementmetathesisaskeysteps
AT ravikumarongolu synthesisofatricycliclactamviabeckmannrearrangementandringrearrangementmetathesisaskeysteps
AT majhijadab synthesisofatricycliclactamviabeckmannrearrangementandringrearrangementmetathesisaskeysteps

Ejemplares similares