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N,N’-Carbonyldiimidazole as a reagent of choice for the synthesis of thienyl-substituted pyrrolidine-2,5-diones

Mikhail Mikhailovich Krayushkin 1
Mikhail Mikhailovich Krayushkin
, 
Feliks Markelovich Stojanovich 1
Feliks Markelovich Stojanovich
, 
Sergei Valer'evich Shorunov 1
Sergei Valer'evich Shorunov
10.1070/MC2003v013n04ABEH001761
Published 2003-09-02
Communication , Volume 13, Issue 4, 192-193
8
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Krayushkin M. M., Stojanovich F. M., Shorunov S. V. N,N’-Carbonyldiimidazole as a reagent of choice for the synthesis of thienyl-substituted pyrrolidine-2,5-diones // Mendeleev Communications. 2003. Vol. 13. No. 4. pp. 192-193.
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Krayushkin M. M., Stojanovich F. M., Shorunov S. V. N,N’-Carbonyldiimidazole as a reagent of choice for the synthesis of thienyl-substituted pyrrolidine-2,5-diones // Mendeleev Communications. 2003. Vol. 13. No. 4. pp. 192-193.
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TY - JOUR
DO - 10.1070/MC2003v013n04ABEH001761
UR - https://mendcomm.colab.ws/publications/10.1070/MC2003v013n04ABEH001761
TI - N,N’-Carbonyldiimidazole as a reagent of choice for the synthesis of thienyl-substituted pyrrolidine-2,5-diones
T2 - Mendeleev Communications
AU - Krayushkin, Mikhail Mikhailovich
AU - Stojanovich, Feliks Markelovich
AU - Shorunov, Sergei Valer'evich
PY - 2003
DA - 2003/09/02
PB - Mendeleev Communications
SP - 192-193
IS - 4
VL - 13
ER -
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@article{2003_Krayushkin,
author = {Mikhail Mikhailovich Krayushkin and Feliks Markelovich Stojanovich and Sergei Valer'evich Shorunov},
title = {N,N’-Carbonyldiimidazole as a reagent of choice for the synthesis of thienyl-substituted pyrrolidine-2,5-diones},
journal = {Mendeleev Communications},
year = {2003},
volume = {13},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2003v013n04ABEH001761},
number = {4},
pages = {192--193},
doi = {10.1070/MC2003v013n04ABEH001761}
}
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Krayushkin, Mikhail Mikhailovich, et al. “N,N’-Carbonyldiimidazole as a reagent of choice for the synthesis of thienyl-substituted pyrrolidine-2,5-diones.” Mendeleev Communications, vol. 13, no. 4, Sep. 2003, pp. 192-193. https://mendcomm.colab.ws/publications/10.1070/MC2003v013n04ABEH001761.

Abstract

N-tert-Butyloxycarbonylamino-3-[Z-α-(2,5-dimethyl-3-thienyl)ethylidene]-4-isopropylidenepyrrolidine-2,5-dione was prepared in 80% yield from the corresponding isomeric hydrazidic acids using N,N’-carbonyldiimidazole, whereas a number of other cyclisation reagents were ineffective.

References

1.
Photochromic heterocyclic fulgides. Part 4. The thermal and photochemical reactions of (E)-isopropylidene-[α-(2- and -(3-thienyl)ethylidene]succinic anhydrides and related compounds
Glaze A.P., Harris S.A., Heller H.G., Johncock W., Oliver S.N., Strydom P.J., Whittall J.
Journal of the Chemical Society Perkin Transactions 1, 1985
2.
The Synthesis of N-Substituted Isomaleimides
COTTER R.J., SAUERS C.K., WHELAN J.M.
Journal of Organic Chemistry, 1961
4.
Ti(o-i-pr)4 mediated lactamizations
Mader M., Helquist P.
Tetrahedron Letters, 1988
6.
Stereoselective nucleophilic additions to the carbon-nitrogen double bond. 3. Chiral acyliminium ions
Polniaszek R.P., Belmont S.E., Alvarez R.
Journal of Organic Chemistry, 1990
7.
Acylation of lycoctonine: Semi-synthesis of inuline, delsemine analogues and methyllycaconitine
Blagbrough I.S., Coates P.A., Hardick D.J., Lewis T., Rowan M.G., Wonnacott S., Potter B.V.
Tetrahedron Letters, 1994