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Negative ion liquid secondary ion mass spectrometry of carbamate‐linked oligodeoxynucleosides. II
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Zeitschriftentitel: | Organic Mass Spectrometry |
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Personen und Körperschaften: | , , , , |
In: | Organic Mass Spectrometry, 25, 1990, 4, S. 219-224 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
Wiley
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Schlagwörter: |
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. |
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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 |
doi_str_mv |
10.1002/oms.1210250408 |
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Online |
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Medizin Chemie und Pharmazie Allgemeines Technik |
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Wiley, 1990 |
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Wiley, 1990 |
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0030-493X |
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0030-493X |
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English |
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Wiley (CrossRef) |
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1990 |
publisher |
Wiley |
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ai |
series |
Organic Mass Spectrometry |
source_id |
49 |
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. |
container_issue | 4 |
container_start_page | 219 |
container_title | Organic Mass Spectrometry |
container_volume | 25 |
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> |
doi_str_mv | 10.1002/oms.1210250408 |
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finc_class_facet | Medizin, Chemie und Pharmazie, Allgemeines, Technik |
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format_dezwi2 | Article, E-Article |
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id | ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9vbXMuMTIxMDI1MDQwOA |
imprint | Wiley, 1990 |
imprint_str_mv | Wiley, 1990 |
institution | DE-Bn3, DE-Brt1, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275 |
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issn_str_mv | 0030-493X |
language | English |
last_indexed | 2024-03-01T15:08:05.583Z |
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mega_collection | Wiley (CrossRef) |
physical | 219-224 |
publishDate | 1990 |
publishDateSort | 1990 |
publisher | Wiley |
record_format | ai |
recordtype | ai |
series | Organic Mass Spectrometry |
source_id | 49 |
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 |