author_facet Laramée, James A.
Arbogast, Brian
Stirchak, Eugene P.
Weller, Dwight D.
Deinzer, Max L.
Laramée, James A.
Arbogast, Brian
Stirchak, Eugene P.
Weller, Dwight D.
Deinzer, Max L.
author Laramée, James A.
Arbogast, Brian
Stirchak, Eugene P.
Weller, Dwight D.
Deinzer, Max L.
spellingShingle Laramée, James A.
Arbogast, Brian
Stirchak, Eugene P.
Weller, Dwight D.
Deinzer, Max L.
Organic Mass Spectrometry
Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
Instrumentation
Molecular Medicine
Biochemistry
author_sort laramée, james a.
spelling Laramée, James A. Arbogast, Brian Stirchak, Eugene P. Weller, Dwight D. Deinzer, Max L. 0030-493X Wiley Instrumentation Molecular Medicine Biochemistry http://dx.doi.org/10.1002/oms.1210250408 <jats:title>Abstract</jats:title><jats:p>Carbamate‐linked Oligodeoxynucleosides, in which the backbone consists of carbamate and <jats:italic>N</jats:italic>‐methylcarbamate linkages, have been analyzed by negative ion liquid secondary ion mass spectrometry. Bidirectional sequence‐determining fragmentations are postulated to occur from a common radical anion intermediate that is produced by capture of an ionizing electron by the neutral sample molecule. Fragmentation reactions appear to be related to whether a proton or methyl group is present on the amide nitrogen.</jats:p> Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II Organic Mass Spectrometry
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series Organic Mass Spectrometry
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title Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
title_unstemmed Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
title_full Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
title_fullStr Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
title_full_unstemmed Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
title_short Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
title_sort negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. ii
topic Instrumentation
Molecular Medicine
Biochemistry
url http://dx.doi.org/10.1002/oms.1210250408
publishDate 1990
physical 219-224
description <jats:title>Abstract</jats:title><jats:p>Carbamate‐linked Oligodeoxynucleosides, in which the backbone consists of carbamate and <jats:italic>N</jats:italic>‐methylcarbamate linkages, have been analyzed by negative ion liquid secondary ion mass spectrometry. Bidirectional sequence‐determining fragmentations are postulated to occur from a common radical anion intermediate that is produced by capture of an ionizing electron by the neutral sample molecule. Fragmentation reactions appear to be related to whether a proton or methyl group is present on the amide nitrogen.</jats:p>
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author Laramée, James A., Arbogast, Brian, Stirchak, Eugene P., Weller, Dwight D., Deinzer, Max L.
author_facet Laramée, James A., Arbogast, Brian, Stirchak, Eugene P., Weller, Dwight D., Deinzer, Max L., Laramée, James A., Arbogast, Brian, Stirchak, Eugene P., Weller, Dwight D., Deinzer, Max L.
author_sort laramée, james a.
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description <jats:title>Abstract</jats:title><jats:p>Carbamate‐linked Oligodeoxynucleosides, in which the backbone consists of carbamate and <jats:italic>N</jats:italic>‐methylcarbamate linkages, have been analyzed by negative ion liquid secondary ion mass spectrometry. Bidirectional sequence‐determining fragmentations are postulated to occur from a common radical anion intermediate that is produced by capture of an ionizing electron by the neutral sample molecule. Fragmentation reactions appear to be related to whether a proton or methyl group is present on the amide nitrogen.</jats:p>
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spelling Laramée, James A. Arbogast, Brian Stirchak, Eugene P. Weller, Dwight D. Deinzer, Max L. 0030-493X Wiley Instrumentation Molecular Medicine Biochemistry http://dx.doi.org/10.1002/oms.1210250408 <jats:title>Abstract</jats:title><jats:p>Carbamate‐linked Oligodeoxynucleosides, in which the backbone consists of carbamate and <jats:italic>N</jats:italic>‐methylcarbamate linkages, have been analyzed by negative ion liquid secondary ion mass spectrometry. Bidirectional sequence‐determining fragmentations are postulated to occur from a common radical anion intermediate that is produced by capture of an ionizing electron by the neutral sample molecule. Fragmentation reactions appear to be related to whether a proton or methyl group is present on the amide nitrogen.</jats:p> Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II Organic Mass Spectrometry
spellingShingle Laramée, James A., Arbogast, Brian, Stirchak, Eugene P., Weller, Dwight D., Deinzer, Max L., Organic Mass Spectrometry, Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II, Instrumentation, Molecular Medicine, Biochemistry
title Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
title_full Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
title_fullStr Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
title_full_unstemmed Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
title_short Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
title_sort negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. ii
title_unstemmed Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
topic Instrumentation, Molecular Medicine, Biochemistry
url http://dx.doi.org/10.1002/oms.1210250408