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Alkylation of substituted 2,5-dihydropyrrol-2-ones at the 3- and 5-positions

Kirill Valentinovich Nikitin 1
Kirill Valentinovich Nikitin
, 
Nonna Petrovna Andryukhova 1
Nonna Petrovna Andryukhova
10.1070/MC1999v009n04ABEH001150
Published 1999-07-09
Communication , Volume 9, Issue 4, 168-170
4
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Nikitin K. V., Andryukhova N. P. Alkylation of substituted 2,5-dihydropyrrol-2-ones at the 3- and 5-positions // Mendeleev Communications. 1999. Vol. 9. No. 4. pp. 168-170.
GOST all authors (up to 50) Copy
Nikitin K. V., Andryukhova N. P. Alkylation of substituted 2,5-dihydropyrrol-2-ones at the 3- and 5-positions // Mendeleev Communications. 1999. Vol. 9. No. 4. pp. 168-170.
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TY - JOUR
DO - 10.1070/MC1999v009n04ABEH001150
UR - https://mendcomm.colab.ws/publications/10.1070/MC1999v009n04ABEH001150
TI - Alkylation of substituted 2,5-dihydropyrrol-2-ones at the 3- and 5-positions
T2 - Mendeleev Communications
AU - Nikitin, Kirill Valentinovich
AU - Andryukhova, Nonna Petrovna
PY - 1999
DA - 1999/07/09
PB - Mendeleev Communications
SP - 168-170
IS - 4
VL - 9
ER -
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@article{1999_Nikitin,
author = {Kirill Valentinovich Nikitin and Nonna Petrovna Andryukhova},
title = {Alkylation of substituted 2,5-dihydropyrrol-2-ones at the 3- and 5-positions},
journal = {Mendeleev Communications},
year = {1999},
volume = {9},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1999v009n04ABEH001150},
number = {4},
pages = {168--170},
doi = {10.1070/MC1999v009n04ABEH001150}
}
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Nikitin, Kirill Valentinovich, and Nonna Petrovna Andryukhova. “Alkylation of substituted 2,5-dihydropyrrol-2-ones at the 3- and 5-positions.” Mendeleev Communications, vol. 9, no. 4, Jul. 1999, pp. 168-170. https://mendcomm.colab.ws/publications/10.1070/MC1999v009n04ABEH001150.

Abstract

The alkylation and Michael reaction of dihydropyrrol-2-ones have been performed under mild conditions.

References

1.
B. Boehner and M. Baumann, Swiss Patent, 633678, 1982 (Chem. Abstr., 1982, 98, 121386).
2.
T. Kume, T. Goto, M. Honmachida, A. Kamochi, A. Yanagi, S. Yagi and S. Miyachi, European Patent, 0286816 A1, 1989 (Chem. Abstr., 1989, 110, 135246).
3.
B. Boehner and M. Baumann, German Patent, 2735841 A1, 1978 (Chem. Abstr., 1978, 88, 152415).
4.
Total synthesis of pukeleimide A, a 5-ylidenepyrrol-2(5H)-one from blue green algae
James G.D., Mills S.D., Pattenden G.
Journal of the Chemical Society Perkin Transactions 1, 1993
5.
10.1070/MC1999v009n04ABEH001150_bib5
Gill
J. Chem. Soc., Perkin Trans. 1, 1993
6.
New protocols for the synthesis of substituted 4-O-methyl tetramates
Jones R.C., Patience J.M.
Journal of the Chemical Society Perkin Transactions 1, 1990
7.
Diastereoselective bis-alkylation of chiral non-racemic α,β-unsaturated γ-lactams
Baussanne I., Chiaroni A., Husson H., Riche C., Royer J.
Tetrahedron Letters, 1994