Russian Journal of Organic Chemistry

, volume 48 , issue 5 , pages 694-698

Five-membered 2,3-dioxoheterocycles: LXXXVI. spiro-heterocyclization of 1-aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones under the action of 3-arylamino-1H-inden-1-ones. Crystal and molecular structure of 4′-hydroxy-3′-(2,4-dimethylbenzoyl)-1,1′-diphenyl-1H- spiro[indeno[1,2-b]pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-trione

N V Bubnov ¹

E S Denislamova ²

P S Silaichev ^{1, 2}

P A Slepukhin ³

A N Maslivets ^{1, 2}

Hide authors affiliations Show authors affiliations: 3 affiliations

Institute of Natural Sciences at Perm State University, Perm, Russia |

Perm State University, Perm, Russia |

Postovskii Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, Yekaterinburg, Russia |

Publication type: Journal Article

Publication date: 2012-05-01

Pleiades Publishing

Russian Journal of Organic Chemistry

scimago Q4

wos Q4

SJR: 0.190

CiteScore: 1.3

Impact factor: 0.9

ISSN: 10704280, 16083393

DOI: 10.1134/S1070428012050119

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Organic Chemistry

Abstract

Abstract1-Aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones react with 3-arylamino-1H-inden-1-ones affording 1,1′-diaryl-3′-aroyl-4′-hydroxy-1H-spiro[indeno[1,2-b]pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-triones. The crystal and molecular structure of 4′-hydroxy-3′-(2,4-dimethylbenzoyl)-1,1′-diphenyl-1H-spiro[indeno[1,2-b] pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-trione.

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2 citations

Maslivets Andrey

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DSc in Chemistry, professor

346 publications, 1 766 citations, 1 review

h-index: 14

Perm State National Research University

Research interests

Organic Chemistry

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Bubnov N. V. et al. Five-membered 2,3-dioxoheterocycles: LXXXVI. spiro-heterocyclization of 1-aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones under the action of 3-arylamino-1H-inden-1-ones. Crystal and molecular structure of 4′-hydroxy-3′-(2,4-dimethylbenzoyl)-1,1′-diphenyl-1H- spiro[indeno[1,2-b]pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-trione // Russian Journal of Organic Chemistry. 2012. Vol. 48. No. 5. pp. 694-698.

GOST all authors (up to 50) Copy

Bubnov N. V., Denislamova E. S., Silaichev P. S., Slepukhin P. A., Maslivets A. N. Five-membered 2,3-dioxoheterocycles: LXXXVI. spiro-heterocyclization of 1-aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones under the action of 3-arylamino-1H-inden-1-ones. Crystal and molecular structure of 4′-hydroxy-3′-(2,4-dimethylbenzoyl)-1,1′-diphenyl-1H- spiro[indeno[1,2-b]pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-trione // Russian Journal of Organic Chemistry. 2012. Vol. 48. No. 5. pp. 694-698.

RIS |

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RIS Copy

TY - JOUR

DO - 10.1134/S1070428012050119

UR - http://link.springer.com/10.1134/S1070428012050119

TI - Five-membered 2,3-dioxoheterocycles: LXXXVI. spiro-heterocyclization of 1-aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones under the action of 3-arylamino-1H-inden-1-ones. Crystal and molecular structure of 4′-hydroxy-3′-(2,4-dimethylbenzoyl)-1,1′-diphenyl-1H- spiro[indeno[1,2-b]pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-trione

T2 - Russian Journal of Organic Chemistry

AU - Bubnov, N V

AU - Denislamova, E S

AU - Silaichev, P S

AU - Slepukhin, P A

AU - Maslivets, A N

PY - 2012

DA - 2012/05/01

PB - Pleiades Publishing

SP - 694-698

IS - 5

VL - 48

SN - 1070-4280

SN - 1608-3393

ER -

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BibTex (up to 50 authors) Copy

@article{2012_Bubnov,

author = {N V Bubnov and E S Denislamova and P S Silaichev and P A Slepukhin and A N Maslivets},

title = {Five-membered 2,3-dioxoheterocycles: LXXXVI. spiro-heterocyclization of 1-aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones under the action of 3-arylamino-1H-inden-1-ones. Crystal and molecular structure of 4′-hydroxy-3′-(2,4-dimethylbenzoyl)-1,1′-diphenyl-1H- spiro[indeno[1,2-b]pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-trione},

journal = {Russian Journal of Organic Chemistry},

year = {2012},

volume = {48},

publisher = {Pleiades Publishing},

month = {may},

url = {http://link.springer.com/10.1134/S1070428012050119},

number = {5},

pages = {694--698},

doi = {10.1134/S1070428012050119}

}

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Bubnov, N. V., et al. “Five-membered 2,3-dioxoheterocycles: LXXXVI. spiro-heterocyclization of 1-aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones under the action of 3-arylamino-1H-inden-1-ones. Crystal and molecular structure of 4′-hydroxy-3′-(2,4-dimethylbenzoyl)-1,1′-diphenyl-1H- spiro[indeno[1,2-b]pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-trione.” Russian Journal of Organic Chemistry, vol. 48, no. 5, May. 2012, pp. 694-698. http://link.springer.com/10.1134/S1070428012050119.