First example of [3+2] cycloaddition of azomethine ylides to 5-methylidene-3-phenylhydantoin
Publication type: Journal Article
Publication date: 2019-11-01
scimago Q3
SJR: 0.305
CiteScore: 2.8
Impact factor: —
ISSN: 10665285, 15739171
General Chemistry
Abstract
New type dispiroindolinones, dispiroimidazolidine-4,3′-pyrrolidine-2′,3″-indolinones unsubstituted at position 4′ of the central pyrrolidine ring, were synthesized by the 1,3-dipolar cycloaddition of azomethine ylides, generated from N-alkyl-substituted amino acids and isatines, to 5-methylidene-substituted 3-phenylhydantoin.
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Kukushkin M. E. et al. First example of [3+2] cycloaddition of azomethine ylides to 5-methylidene-3-phenylhydantoin // Russian Chemical Bulletin. 2019. Vol. 68. No. 11. pp. 2088-2091.
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Kukushkin M. E., Kondratyeva A. A., Zyk N. V., Majouga A. G., Beloglazkina E. K. First example of [3+2] cycloaddition of azomethine ylides to 5-methylidene-3-phenylhydantoin // Russian Chemical Bulletin. 2019. Vol. 68. No. 11. pp. 2088-2091.
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TY - JOUR
DO - 10.1007/s11172-019-2670-5
UR - http://link.springer.com/10.1007/s11172-019-2670-5
TI - First example of [3+2] cycloaddition of azomethine ylides to 5-methylidene-3-phenylhydantoin
T2 - Russian Chemical Bulletin
AU - Kukushkin, M E
AU - Kondratyeva, A A
AU - Zyk, N. V.
AU - Majouga, A G
AU - Beloglazkina, E K
PY - 2019
DA - 2019/11/01
PB - Springer Nature
SP - 2088-2091
IS - 11
VL - 68
SN - 1066-5285
SN - 1573-9171
ER -
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@article{2019_Kukushkin,
author = {M E Kukushkin and A A Kondratyeva and N. V. Zyk and A G Majouga and E K Beloglazkina},
title = {First example of [3+2] cycloaddition of azomethine ylides to 5-methylidene-3-phenylhydantoin},
journal = {Russian Chemical Bulletin},
year = {2019},
volume = {68},
publisher = {Springer Nature},
month = {nov},
url = {http://link.springer.com/10.1007/s11172-019-2670-5},
number = {11},
pages = {2088--2091},
doi = {10.1007/s11172-019-2670-5}
}
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MLA
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Kukushkin, M. E., et al. “First example of [3+2] cycloaddition of azomethine ylides to 5-methylidene-3-phenylhydantoin.” Russian Chemical Bulletin, vol. 68, no. 11, Nov. 2019, pp. 2088-2091. http://link.springer.com/10.1007/s11172-019-2670-5.