Application of continuous flow technology to the expedient synthesis of isotopically substituted compounds

Isotopically modified compounds are of great importance to the scientific community owing to the large number of specific uses that exist for them; however, due to their low abundance associated costs are high. Once a small discrete isotopic precursor has been obtained, it must then be incorporated...

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Main Author: Hooper, Julian
Other Authors: Watts, Paul
Published: University of Hull 2008
Subjects:
Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.494863
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spelling ndltd-bl.uk-oai-ethos.bl.uk-4948632015-03-20T04:39:39ZApplication of continuous flow technology to the expedient synthesis of isotopically substituted compoundsHooper, JulianWatts, Paul2008Isotopically modified compounds are of great importance to the scientific community owing to the large number of specific uses that exist for them; however, due to their low abundance associated costs are high. Once a small discrete isotopic precursor has been obtained, it must then be incorporated into a more complex molecule at the desired position which creates a major synthetic challenge owing to their limited availability. The difficulties encountered when obtaining isotopically enriched compounds result in phenomenal costs that mean even small quantities of simple molecules are extremely expensive to prepare; thus there is a need for expedient, cost effective and transferable syntheses involving isotopes. In contrast to traditional synthetic techniques, continuous flow systems provide a superior route to the preparation of such molecules viz allowing the use of small, highly contained systems, stoichiometric quantities of reagents and generic methodology to deliver products in high yields and purities. The work contained herein exemplifies that by applying small scale, continuous flow technology to the traditional problems of synthesis involving isotopes, either stable or unstable, new developments can be realised which allow the rapid, efficient, controlled and contained preparation of labelled molecules. General procedures have been developed which allow for the synthesis of isotopically substituted phenyl acetate, methoxybenzene, N-phenylacetamide and biphenyl derivatives in a timely manner using continuous flow systems. As proof of concept, small libraries comprising of compounds containing deuterium isotope labels were successfully prepared, generally in yields greater than 90% at a scale of 10’s mg.541.3884ChemistryUniversity of Hullhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.494863http://hydra.hull.ac.uk/resources/hull:748Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 541.3884
Chemistry
spellingShingle 541.3884
Chemistry
Hooper, Julian
Application of continuous flow technology to the expedient synthesis of isotopically substituted compounds
description Isotopically modified compounds are of great importance to the scientific community owing to the large number of specific uses that exist for them; however, due to their low abundance associated costs are high. Once a small discrete isotopic precursor has been obtained, it must then be incorporated into a more complex molecule at the desired position which creates a major synthetic challenge owing to their limited availability. The difficulties encountered when obtaining isotopically enriched compounds result in phenomenal costs that mean even small quantities of simple molecules are extremely expensive to prepare; thus there is a need for expedient, cost effective and transferable syntheses involving isotopes. In contrast to traditional synthetic techniques, continuous flow systems provide a superior route to the preparation of such molecules viz allowing the use of small, highly contained systems, stoichiometric quantities of reagents and generic methodology to deliver products in high yields and purities. The work contained herein exemplifies that by applying small scale, continuous flow technology to the traditional problems of synthesis involving isotopes, either stable or unstable, new developments can be realised which allow the rapid, efficient, controlled and contained preparation of labelled molecules. General procedures have been developed which allow for the synthesis of isotopically substituted phenyl acetate, methoxybenzene, N-phenylacetamide and biphenyl derivatives in a timely manner using continuous flow systems. As proof of concept, small libraries comprising of compounds containing deuterium isotope labels were successfully prepared, generally in yields greater than 90% at a scale of 10’s mg.
author2 Watts, Paul
author_facet Watts, Paul
Hooper, Julian
author Hooper, Julian
author_sort Hooper, Julian
title Application of continuous flow technology to the expedient synthesis of isotopically substituted compounds
title_short Application of continuous flow technology to the expedient synthesis of isotopically substituted compounds
title_full Application of continuous flow technology to the expedient synthesis of isotopically substituted compounds
title_fullStr Application of continuous flow technology to the expedient synthesis of isotopically substituted compounds
title_full_unstemmed Application of continuous flow technology to the expedient synthesis of isotopically substituted compounds
title_sort application of continuous flow technology to the expedient synthesis of isotopically substituted compounds
publisher University of Hull
publishDate 2008
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.494863
work_keys_str_mv AT hooperjulian applicationofcontinuousflowtechnologytotheexpedientsynthesisofisotopicallysubstitutedcompounds
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