Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]
Abstract 4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. The molecular and crystal structures of 4′,5′-dibenzoyl-1′-(4-methoxyp...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Antonov, D. I. [verfasserIn] Dmitriev, M. V. [verfasserIn] Maslivets, A. N. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2019 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Russian journal of organic chemistry - Dordrecht : Springer Science + Business Media B.V., 1996, 55(2019), 7 vom: Juli, Seite 933-937 |
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| Übergeordnetes Werk: |
volume:55 ; year:2019 ; number:7 ; month:07 ; pages:933-937 |
| Links: |
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| DOI / URN: |
10.1134/S1070428019070029 |
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| Katalog-ID: |
SPR017516587 |
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| 100 | 1 | |a Antonov, D. I. |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] |
| 264 | 1 | |c 2019 | |
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| 520 | |a Abstract 4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. The molecular and crystal structures of 4′,5′-dibenzoyl-1′-(4-methoxyphenyl)-5-phenyl-5H-spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrrole]-2′,10,12(1′H)-trione were determined by X-ray analysis. | ||
| 650 | 4 | |a 4-benzoyl-1 |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a -pyrrole-2,3-diones |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a cyclic enamines |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a five-membered enamines |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a spiro heterocyclization |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a diindenopyridines |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Dmitriev, M. V. |e verfasserin |4 aut | |
| 700 | 1 | |a Maslivets, A. N. |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Russian journal of organic chemistry |d Dordrecht : Springer Science + Business Media B.V., 1996 |g 55(2019), 7 vom: Juli, Seite 933-937 |w (DE-627)340148543 |w (DE-600)2065669-5 |x 1608-3393 |7 nnns |
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| 912 | |a GBV_ILN_2068 | ||
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10.1134/S1070428019070029 doi (DE-627)SPR017516587 (SPR)S1070428019070029-e DE-627 ger DE-627 rakwb eng 540 ASE 35.50 bkl Antonov, D. I. verfasserin aut Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract 4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. The molecular and crystal structures of 4′,5′-dibenzoyl-1′-(4-methoxyphenyl)-5-phenyl-5H-spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrrole]-2′,10,12(1′H)-trione were determined by X-ray analysis. 4-benzoyl-1 (dpeaa)DE-He213 -pyrrole-2,3-diones (dpeaa)DE-He213 cyclic enamines (dpeaa)DE-He213 five-membered enamines (dpeaa)DE-He213 spiro heterocyclization (dpeaa)DE-He213 diindenopyridines (dpeaa)DE-He213 Dmitriev, M. V. verfasserin aut Maslivets, A. N. verfasserin aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 55(2019), 7 vom: Juli, Seite 933-937 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:55 year:2019 number:7 month:07 pages:933-937 https://dx.doi.org/10.1134/S1070428019070029 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.50 ASE AR 55 2019 7 07 933-937 |
| spelling |
10.1134/S1070428019070029 doi (DE-627)SPR017516587 (SPR)S1070428019070029-e DE-627 ger DE-627 rakwb eng 540 ASE 35.50 bkl Antonov, D. I. verfasserin aut Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract 4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. The molecular and crystal structures of 4′,5′-dibenzoyl-1′-(4-methoxyphenyl)-5-phenyl-5H-spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrrole]-2′,10,12(1′H)-trione were determined by X-ray analysis. 4-benzoyl-1 (dpeaa)DE-He213 -pyrrole-2,3-diones (dpeaa)DE-He213 cyclic enamines (dpeaa)DE-He213 five-membered enamines (dpeaa)DE-He213 spiro heterocyclization (dpeaa)DE-He213 diindenopyridines (dpeaa)DE-He213 Dmitriev, M. V. verfasserin aut Maslivets, A. N. verfasserin aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 55(2019), 7 vom: Juli, Seite 933-937 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:55 year:2019 number:7 month:07 pages:933-937 https://dx.doi.org/10.1134/S1070428019070029 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.50 ASE AR 55 2019 7 07 933-937 |
| allfields_unstemmed |
10.1134/S1070428019070029 doi (DE-627)SPR017516587 (SPR)S1070428019070029-e DE-627 ger DE-627 rakwb eng 540 ASE 35.50 bkl Antonov, D. I. verfasserin aut Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract 4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. The molecular and crystal structures of 4′,5′-dibenzoyl-1′-(4-methoxyphenyl)-5-phenyl-5H-spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrrole]-2′,10,12(1′H)-trione were determined by X-ray analysis. 4-benzoyl-1 (dpeaa)DE-He213 -pyrrole-2,3-diones (dpeaa)DE-He213 cyclic enamines (dpeaa)DE-He213 five-membered enamines (dpeaa)DE-He213 spiro heterocyclization (dpeaa)DE-He213 diindenopyridines (dpeaa)DE-He213 Dmitriev, M. V. verfasserin aut Maslivets, A. N. verfasserin aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 55(2019), 7 vom: Juli, Seite 933-937 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:55 year:2019 number:7 month:07 pages:933-937 https://dx.doi.org/10.1134/S1070428019070029 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.50 ASE AR 55 2019 7 07 933-937 |
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10.1134/S1070428019070029 doi (DE-627)SPR017516587 (SPR)S1070428019070029-e DE-627 ger DE-627 rakwb eng 540 ASE 35.50 bkl Antonov, D. I. verfasserin aut Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract 4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. The molecular and crystal structures of 4′,5′-dibenzoyl-1′-(4-methoxyphenyl)-5-phenyl-5H-spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrrole]-2′,10,12(1′H)-trione were determined by X-ray analysis. 4-benzoyl-1 (dpeaa)DE-He213 -pyrrole-2,3-diones (dpeaa)DE-He213 cyclic enamines (dpeaa)DE-He213 five-membered enamines (dpeaa)DE-He213 spiro heterocyclization (dpeaa)DE-He213 diindenopyridines (dpeaa)DE-He213 Dmitriev, M. V. verfasserin aut Maslivets, A. N. verfasserin aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 55(2019), 7 vom: Juli, Seite 933-937 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:55 year:2019 number:7 month:07 pages:933-937 https://dx.doi.org/10.1134/S1070428019070029 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.50 ASE AR 55 2019 7 07 933-937 |
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10.1134/S1070428019070029 doi (DE-627)SPR017516587 (SPR)S1070428019070029-e DE-627 ger DE-627 rakwb eng 540 ASE 35.50 bkl Antonov, D. I. verfasserin aut Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract 4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. The molecular and crystal structures of 4′,5′-dibenzoyl-1′-(4-methoxyphenyl)-5-phenyl-5H-spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrrole]-2′,10,12(1′H)-trione were determined by X-ray analysis. 4-benzoyl-1 (dpeaa)DE-He213 -pyrrole-2,3-diones (dpeaa)DE-He213 cyclic enamines (dpeaa)DE-He213 five-membered enamines (dpeaa)DE-He213 spiro heterocyclization (dpeaa)DE-He213 diindenopyridines (dpeaa)DE-He213 Dmitriev, M. V. verfasserin aut Maslivets, A. N. verfasserin aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 55(2019), 7 vom: Juli, Seite 933-937 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:55 year:2019 number:7 month:07 pages:933-937 https://dx.doi.org/10.1134/S1070428019070029 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.50 ASE AR 55 2019 7 07 933-937 |
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Enthalten in Russian journal of organic chemistry 55(2019), 7 vom: Juli, Seite 933-937 volume:55 year:2019 number:7 month:07 pages:933-937 |
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4-benzoyl-1 -pyrrole-2,3-diones cyclic enamines five-membered enamines spiro heterocyclization diindenopyridines |
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Russian journal of organic chemistry |
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Antonov, D. I. @@aut@@ Dmitriev, M. V. @@aut@@ Maslivets, A. N. @@aut@@ |
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I.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2019</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract 4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. 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|
| author |
Antonov, D. I. |
| spellingShingle |
Antonov, D. I. ddc 540 bkl 35.50 misc 4-benzoyl-1 misc -pyrrole-2,3-diones misc cyclic enamines misc five-membered enamines misc spiro heterocyclization misc diindenopyridines Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] |
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540 - Chemistry & allied sciences |
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1608-3393 |
| topic_title |
540 ASE 35.50 bkl Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] 4-benzoyl-1 (dpeaa)DE-He213 -pyrrole-2,3-diones (dpeaa)DE-He213 cyclic enamines (dpeaa)DE-He213 five-membered enamines (dpeaa)DE-He213 spiro heterocyclization (dpeaa)DE-He213 diindenopyridines (dpeaa)DE-He213 |
| topic |
ddc 540 bkl 35.50 misc 4-benzoyl-1 misc -pyrrole-2,3-diones misc cyclic enamines misc five-membered enamines misc spiro heterocyclization misc diindenopyridines |
| topic_unstemmed |
ddc 540 bkl 35.50 misc 4-benzoyl-1 misc -pyrrole-2,3-diones misc cyclic enamines misc five-membered enamines misc spiro heterocyclization misc diindenopyridines |
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ddc 540 bkl 35.50 misc 4-benzoyl-1 misc -pyrrole-2,3-diones misc cyclic enamines misc five-membered enamines misc spiro heterocyclization misc diindenopyridines |
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Russian journal of organic chemistry |
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540 - Chemistry |
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Russian journal of organic chemistry |
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| title |
Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] |
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(DE-627)SPR017516587 (SPR)S1070428019070029-e |
| title_full |
Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] |
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Antonov, D. I. |
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Russian journal of organic chemistry |
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Russian journal of organic chemistry |
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eng |
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Antonov, D. I. Dmitriev, M. V. Maslivets, A. N. |
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540 ASE 35.50 bkl |
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Elektronische Aufsätze |
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Antonov, D. I. |
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10.1134/S1070428019070029 |
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540 |
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verfasserin |
| title_sort |
three-component spiro heterocyclization of pyrrolediones with aminoindenones. synthesis of spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] |
| title_auth |
Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] |
| abstract |
Abstract 4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. The molecular and crystal structures of 4′,5′-dibenzoyl-1′-(4-methoxyphenyl)-5-phenyl-5H-spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrrole]-2′,10,12(1′H)-trione were determined by X-ray analysis. |
| abstractGer |
Abstract 4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. The molecular and crystal structures of 4′,5′-dibenzoyl-1′-(4-methoxyphenyl)-5-phenyl-5H-spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrrole]-2′,10,12(1′H)-trione were determined by X-ray analysis. |
| abstract_unstemmed |
Abstract 4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. The molecular and crystal structures of 4′,5′-dibenzoyl-1′-(4-methoxyphenyl)-5-phenyl-5H-spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrrole]-2′,10,12(1′H)-trione were determined by X-ray analysis. |
| collection_details |
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| container_issue |
7 |
| title_short |
Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles] |
| url |
https://dx.doi.org/10.1134/S1070428019070029 |
| remote_bool |
true |
| author2 |
Dmitriev, M. V. Maslivets, A. N. |
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Dmitriev, M. V. Maslivets, A. N. |
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340148543 |
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| doi_str |
10.1134/S1070428019070029 |
| up_date |
2024-07-03T13:24:49.215Z |
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1803564445041950720 |
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|
| score |
7.399352 |