Synthesis of spiro[furo[3,4-b]pyran-4,3′-pyrroles] by reaction of pyrrolediones with malononitrile and tetronic acid
Publication type: Journal Article
Publication date: 2017-01-01
scimago Q4
wos Q4
SJR: 0.190
CiteScore: 1.3
Impact factor: 0.9
ISSN: 10704280, 16083393
Organic Chemistry
Abstract
Substituted ethyl 2-amino-3-cyano-2′,5-dioxo-5′-phenyl-1′,2′,5,7-tetrahydrospiro[furo[3,4-b]pyran-4,3′-pyrrole]-2′-carboxylates were synthesized by one-pot reaction of ethyl 2-phenyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-3-carboxylates with malononitrile and furan-2,4(3H,5H)-dione.
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Salnikova T. V. et al. Synthesis of spiro[furo[3,4-b]pyran-4,3′-pyrroles] by reaction of pyrrolediones with malononitrile and tetronic acid // Russian Journal of Organic Chemistry. 2017. Vol. 53. No. 1. pp. 128-129.
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Salnikova T. V., Dmitriev M. V., Maslivets A. N. Synthesis of spiro[furo[3,4-b]pyran-4,3′-pyrroles] by reaction of pyrrolediones with malononitrile and tetronic acid // Russian Journal of Organic Chemistry. 2017. Vol. 53. No. 1. pp. 128-129.
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TY - JOUR
DO - 10.1134/S1070428017010249
UR - http://link.springer.com/10.1134/S1070428017010249
TI - Synthesis of spiro[furo[3,4-b]pyran-4,3′-pyrroles] by reaction of pyrrolediones with malononitrile and tetronic acid
T2 - Russian Journal of Organic Chemistry
AU - Salnikova, T. V.
AU - Dmitriev, M V
AU - Maslivets, A N
PY - 2017
DA - 2017/01/01
PB - Pleiades Publishing
SP - 128-129
IS - 1
VL - 53
SN - 1070-4280
SN - 1608-3393
ER -
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@article{2017_Salnikova,
author = {T. V. Salnikova and M V Dmitriev and A N Maslivets},
title = {Synthesis of spiro[furo[3,4-b]pyran-4,3′-pyrroles] by reaction of pyrrolediones with malononitrile and tetronic acid},
journal = {Russian Journal of Organic Chemistry},
year = {2017},
volume = {53},
publisher = {Pleiades Publishing},
month = {jan},
url = {http://link.springer.com/10.1134/S1070428017010249},
number = {1},
pages = {128--129},
doi = {10.1134/S1070428017010249}
}
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MLA
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Salnikova, T. V., et al. “Synthesis of spiro[furo[3,4-b]pyran-4,3′-pyrroles] by reaction of pyrrolediones with malononitrile and tetronic acid.” Russian Journal of Organic Chemistry, vol. 53, no. 1, Jan. 2017, pp. 128-129. http://link.springer.com/10.1134/S1070428017010249.
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