Cargando…

Design and synthesis of polycyclic sulfones via Diels–Alder reaction and ring-rearrangement metathesis as key steps

Here, we describe a new and simple synthetic strategy to various polycyclic sulfones via Diels–Alder reaction and ring-rearrangement metathesis (RRM) as the key steps. This approach delivers tri- and tetracyclic sulfones with six (n = 1), seven (n = 2) or eight-membered (n = 3) fused-ring systems co...

Descripción completa

Detalles Bibliográficos
Autores principales: Kotha, Sambasivarao, Gunta, Rama
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578373/
https://www.ncbi.nlm.nih.gov/pubmed/26425192
http://dx.doi.org/10.3762/bjoc.11.148
_version_ 1782391105882423296
author Kotha, Sambasivarao
Gunta, Rama
author_facet Kotha, Sambasivarao
Gunta, Rama
author_sort Kotha, Sambasivarao
collection PubMed
description Here, we describe a new and simple synthetic strategy to various polycyclic sulfones via Diels–Alder reaction and ring-rearrangement metathesis (RRM) as the key steps. This approach delivers tri- and tetracyclic sulfones with six (n = 1), seven (n = 2) or eight-membered (n = 3) fused-ring systems containing trans-ring junctions unlike the conventional all cis-ring junctions generally obtained during the RRM sequence. Interestingly the starting materials used are simple and commercially available.
format Online
Article
Text
id pubmed-4578373
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-45783732015-09-30 Design and synthesis of polycyclic sulfones via Diels–Alder reaction and ring-rearrangement metathesis as key steps Kotha, Sambasivarao Gunta, Rama Beilstein J Org Chem Full Research Paper Here, we describe a new and simple synthetic strategy to various polycyclic sulfones via Diels–Alder reaction and ring-rearrangement metathesis (RRM) as the key steps. This approach delivers tri- and tetracyclic sulfones with six (n = 1), seven (n = 2) or eight-membered (n = 3) fused-ring systems containing trans-ring junctions unlike the conventional all cis-ring junctions generally obtained during the RRM sequence. Interestingly the starting materials used are simple and commercially available. Beilstein-Institut 2015-08-06 /pmc/articles/PMC4578373/ /pubmed/26425192 http://dx.doi.org/10.3762/bjoc.11.148 Text en Copyright © 2015, Kotha and Gunta 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
Gunta, Rama
Design and synthesis of polycyclic sulfones via Diels–Alder reaction and ring-rearrangement metathesis as key steps
title Design and synthesis of polycyclic sulfones via Diels–Alder reaction and ring-rearrangement metathesis as key steps
title_full Design and synthesis of polycyclic sulfones via Diels–Alder reaction and ring-rearrangement metathesis as key steps
title_fullStr Design and synthesis of polycyclic sulfones via Diels–Alder reaction and ring-rearrangement metathesis as key steps
title_full_unstemmed Design and synthesis of polycyclic sulfones via Diels–Alder reaction and ring-rearrangement metathesis as key steps
title_short Design and synthesis of polycyclic sulfones via Diels–Alder reaction and ring-rearrangement metathesis as key steps
title_sort design and synthesis of polycyclic sulfones via diels–alder reaction and ring-rearrangement metathesis as key steps
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578373/
https://www.ncbi.nlm.nih.gov/pubmed/26425192
http://dx.doi.org/10.3762/bjoc.11.148
work_keys_str_mv AT kothasambasivarao designandsynthesisofpolycyclicsulfonesviadielsalderreactionandringrearrangementmetathesisaskeysteps
AT guntarama designandsynthesisofpolycyclicsulfonesviadielsalderreactionandringrearrangementmetathesisaskeysteps