(Z)-Methyl 2-methoxyimino-3-oxobutanoate
The title compound, C6H9NO4, was prepared stereoselectively as a precursor for 1-azadienes in a study of hetero-Diels–Alder reactions. The configuration of the C=N double bond was found to be Z, corroborating earlier assignments of similar compounds based only on NMR and IR spectroscopic a...
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International Union of Crystallography
2008-03-01
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Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536808004376 |
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doaj-deb271becf3f45b483cb20f886a679092020-11-24T21:32:46ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682008-03-01643o602o60210.1107/S1600536808004376(Z)-Methyl 2-methoxyimino-3-oxobutanoateHans-Dieter ArndtHans PreutWei-Zheng ShenJin-Yong LuThe title compound, C6H9NO4, was prepared stereoselectively as a precursor for 1-azadienes in a study of hetero-Diels–Alder reactions. The configuration of the C=N double bond was found to be Z, corroborating earlier assignments of similar compounds based only on NMR and IR spectroscopic analysis.http://scripts.iucr.org/cgi-bin/paper?S1600536808004376 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hans-Dieter Arndt Hans Preut Wei-Zheng Shen Jin-Yong Lu |
spellingShingle |
Hans-Dieter Arndt Hans Preut Wei-Zheng Shen Jin-Yong Lu (Z)-Methyl 2-methoxyimino-3-oxobutanoate Acta Crystallographica Section E |
author_facet |
Hans-Dieter Arndt Hans Preut Wei-Zheng Shen Jin-Yong Lu |
author_sort |
Hans-Dieter Arndt |
title |
(Z)-Methyl 2-methoxyimino-3-oxobutanoate |
title_short |
(Z)-Methyl 2-methoxyimino-3-oxobutanoate |
title_full |
(Z)-Methyl 2-methoxyimino-3-oxobutanoate |
title_fullStr |
(Z)-Methyl 2-methoxyimino-3-oxobutanoate |
title_full_unstemmed |
(Z)-Methyl 2-methoxyimino-3-oxobutanoate |
title_sort |
(z)-methyl 2-methoxyimino-3-oxobutanoate |
publisher |
International Union of Crystallography |
series |
Acta Crystallographica Section E |
issn |
1600-5368 |
publishDate |
2008-03-01 |
description |
The title compound, C6H9NO4, was prepared stereoselectively as a precursor for 1-azadienes in a study of hetero-Diels–Alder reactions. The configuration of the C=N double bond was found to be Z, corroborating earlier assignments of similar compounds based only on NMR and IR spectroscopic analysis. |
url |
http://scripts.iucr.org/cgi-bin/paper?S1600536808004376 |
work_keys_str_mv |
AT hansdieterarndt zmethyl2methoxyimino3oxobutanoate AT hanspreut zmethyl2methoxyimino3oxobutanoate AT weizhengshen zmethyl2methoxyimino3oxobutanoate AT jinyonglu zmethyl2methoxyimino3oxobutanoate |
_version_ |
1725956071010336768 |