Cargando…

Enantiospecific synthesis of [2.2]paracyclophane-4-thiol and derivatives

This paper describes a simple route to enantiomerically enriched [2.2]paracyclophane-4-thiol via the stereospecific introduction of a chiral sulfoxide to the [2.2]paracyclophane skeleton. The first synthesis of an enantiomerically enriched planar chiral benzothiazole is also reported.

Detalles Bibliográficos
Autores principales: Rowlands, Gareth J, Seacome, Richard J
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686273/
https://www.ncbi.nlm.nih.gov/pubmed/19478964
http://dx.doi.org/10.3762/bjoc.5.9
_version_ 1782167389094281216
author Rowlands, Gareth J
Seacome, Richard J
author_facet Rowlands, Gareth J
Seacome, Richard J
author_sort Rowlands, Gareth J
collection PubMed
description This paper describes a simple route to enantiomerically enriched [2.2]paracyclophane-4-thiol via the stereospecific introduction of a chiral sulfoxide to the [2.2]paracyclophane skeleton. The first synthesis of an enantiomerically enriched planar chiral benzothiazole is also reported.
format Text
id pubmed-2686273
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-26862732009-05-28 Enantiospecific synthesis of [2.2]paracyclophane-4-thiol and derivatives Rowlands, Gareth J Seacome, Richard J Beilstein J Org Chem Full Research Paper This paper describes a simple route to enantiomerically enriched [2.2]paracyclophane-4-thiol via the stereospecific introduction of a chiral sulfoxide to the [2.2]paracyclophane skeleton. The first synthesis of an enantiomerically enriched planar chiral benzothiazole is also reported. Beilstein-Institut 2009-03-12 /pmc/articles/PMC2686273/ /pubmed/19478964 http://dx.doi.org/10.3762/bjoc.5.9 Text en Copyright © 2009, Rowlands and Seacome 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
Rowlands, Gareth J
Seacome, Richard J
Enantiospecific synthesis of [2.2]paracyclophane-4-thiol and derivatives
title Enantiospecific synthesis of [2.2]paracyclophane-4-thiol and derivatives
title_full Enantiospecific synthesis of [2.2]paracyclophane-4-thiol and derivatives
title_fullStr Enantiospecific synthesis of [2.2]paracyclophane-4-thiol and derivatives
title_full_unstemmed Enantiospecific synthesis of [2.2]paracyclophane-4-thiol and derivatives
title_short Enantiospecific synthesis of [2.2]paracyclophane-4-thiol and derivatives
title_sort enantiospecific synthesis of [2.2]paracyclophane-4-thiol and derivatives
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686273/
https://www.ncbi.nlm.nih.gov/pubmed/19478964
http://dx.doi.org/10.3762/bjoc.5.9
work_keys_str_mv AT rowlandsgarethj enantiospecificsynthesisof22paracyclophane4thiolandderivatives
AT seacomerichardj enantiospecificsynthesisof22paracyclophane4thiolandderivatives