Research output: Contribution to journal › Article › peer-review
Synthesis of 1-aryl-3a,8b-dihydroxy-3-(1-hydroxyethylidene)-1,3,3a,8b-tetrahydroindeno[1,2-b]pyrrole-2,4-diones. / Yankin, A. N.; Nosova, N. V.; Dmitriev, M. V.; Gein, V. L.
In: Russian Journal of Organic Chemistry, Vol. 52, No. 2, 01.02.2016, p. 206-208.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Synthesis of 1-aryl-3a,8b-dihydroxy-3-(1-hydroxyethylidene)-1,3,3a,8b-tetrahydroindeno[1,2-b]pyrrole-2,4-diones
AU - Yankin, A. N.
AU - Nosova, N. V.
AU - Dmitriev, M. V.
AU - Gein, V. L.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - Reaction of acetoacetic acid N-arylamides with ninhydrin at boiling in ethanol in the presence of iron(III) chloride afforded 1-aryl-3a,8b-dihydroxy-3-(1-hydroxyethylidene)-1,3,3a,8b-tetrahydroindeno[1,2-b]-pyrrole-2,4-diones. The structure of compounds was confirmed by IR, 1H NMR, and mass spectra and X-ray diffraction (XRD) analysis.
AB - Reaction of acetoacetic acid N-arylamides with ninhydrin at boiling in ethanol in the presence of iron(III) chloride afforded 1-aryl-3a,8b-dihydroxy-3-(1-hydroxyethylidene)-1,3,3a,8b-tetrahydroindeno[1,2-b]-pyrrole-2,4-diones. The structure of compounds was confirmed by IR, 1H NMR, and mass spectra and X-ray diffraction (XRD) analysis.
UR - http://www.scopus.com/inward/record.url?scp=84962467437&partnerID=8YFLogxK
U2 - 10.1134/S107042801602007X
DO - 10.1134/S107042801602007X
M3 - Article
AN - SCOPUS:84962467437
VL - 52
SP - 206
EP - 208
JO - Russian Journal of Organic Chemistry
JF - Russian Journal of Organic Chemistry
SN - 1070-4280
IS - 2
ER -
ID: 36325384