A H-1, C-13 and N-15 NMR spectroscopic and GIAO DFT study of ethyl 5-oxo-2-phenyl-4-(phenylhydrazono)-4,5-dihydro-1H-pyrrole-3-carboxylate
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F10%3A39881833" target="_blank" >RIV/00216275:25310/10:39881833 - isvavai.cz</a>
Result on the web
—
DOI - Digital Object Identifier
—
Alternative languages
Result language
angličtina
Original language name
A H-1, C-13 and N-15 NMR spectroscopic and GIAO DFT study of ethyl 5-oxo-2-phenyl-4-(phenylhydrazono)-4,5-dihydro-1H-pyrrole-3-carboxylate
Original language description
15N-Labelled ethyl 5-oxo-2-phenyl-4-(2-phenylhydrazono)-4,5-dihydro-1H-pyrrole-3-carboxylate was synthesized by azo-coupling of diazotized aniline (using Na15NO2, 99% 15N) with ethyl 4,5-dihydro-5oxo-2-phenyl-(1H)-pyrrole-3-carboxylate. The product was formed as a tautomeric hydrazone mixture as con?rmed by 13C and 15N chemical shifts, and was obtained as a mixture of E and Z isomers according to nJ(15N, 13C). A comparison of the 1H NMR data with GIAO DFT calculations enabled determination of the con?guration of the carboxy ester group in both isomers.
Czech name
—
Czech description
—
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—
Result continuities
Project
—
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2010
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Tetrahedron Letters
ISSN
0040-4039
e-ISSN
—
Volume of the periodical
51
Issue of the periodical within the volume
23
Country of publishing house
GB - UNITED KINGDOM
Number of pages
3
Pages from-to
—
UT code for WoS article
000278451000031
EID of the result in the Scopus database
—