Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines
Abstract Relying on the values of the energy of the highest occupied molecular orbitals calculated ab initio a series of reactivity was established for ylides isomeric to 10-methyl-9,10-dihydroacridine, dibenzopyran, dibenzothiopyran, 1,3-benzodithiol, and the tentative threshold value was determine...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Yunnikova, L. P. [verfasserIn] Makhova, T. V. [verfasserIn] Yunnikov, A. L. [verfasserIn] Gorokhov, V. Yu. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2009 |
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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, 45(2009), 5 vom: Mai, Seite 735-739 |
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| Übergeordnetes Werk: |
volume:45 ; year:2009 ; number:5 ; month:05 ; pages:735-739 |
| Links: |
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| DOI / URN: |
10.1134/S1070428009050157 |
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| Katalog-ID: |
SPR017483034 |
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| 100 | 1 | |a Yunnikova, L. P. |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines |
| 264 | 1 | |c 2009 | |
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| 520 | |a Abstract Relying on the values of the energy of the highest occupied molecular orbitals calculated ab initio a series of reactivity was established for ylides isomeric to 10-methyl-9,10-dihydroacridine, dibenzopyran, dibenzothiopyran, 1,3-benzodithiol, and the tentative threshold value was determined for imines reaction with the mentioned heterocycles. One- or two-stage imines interaction with 10-methyl-9,10-dihydroacridine or dibenzopyran was confirmed by two reactions of ionic hydroheterylation of N-benzylideneaniline in the presence of sodium tetrahydroborate by the cation of 10-methyl-9,10-dihydroacridinium or the cation of dibenzopyrylium. | ||
| 650 | 4 | |a Xanthene |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Sodium Tetrahydroborate |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Methyleneaniline |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Thioxanthene |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Protonated Imine |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Makhova, T. V. |e verfasserin |4 aut | |
| 700 | 1 | |a Yunnikov, A. L. |e verfasserin |4 aut | |
| 700 | 1 | |a Gorokhov, V. Yu. |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 45(2009), 5 vom: Mai, Seite 735-739 |w (DE-627)340148543 |w (DE-600)2065669-5 |x 1608-3393 |7 nnns |
| 773 | 1 | 8 | |g volume:45 |g year:2009 |g number:5 |g month:05 |g pages:735-739 |
| 856 | 4 | 0 | |u https://dx.doi.org/10.1134/S1070428009050157 |z lizenzpflichtig |3 Volltext |
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| 912 | |a GBV_ILN_2011 | ||
| 912 | |a GBV_ILN_2014 | ||
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| 912 | |a GBV_ILN_2037 | ||
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| 912 | |a GBV_ILN_2039 | ||
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| 912 | |a GBV_ILN_2056 | ||
| 912 | |a GBV_ILN_2057 | ||
| 912 | |a GBV_ILN_2059 | ||
| 912 | |a GBV_ILN_2061 | ||
| 912 | |a GBV_ILN_2064 | ||
| 912 | |a GBV_ILN_2065 | ||
| 912 | |a GBV_ILN_2068 | ||
| 912 | |a GBV_ILN_2070 | ||
| 912 | |a GBV_ILN_2086 | ||
| 912 | |a GBV_ILN_2088 | ||
| 912 | |a GBV_ILN_2093 | ||
| 912 | |a GBV_ILN_2106 | ||
| 912 | |a GBV_ILN_2107 | ||
| 912 | |a GBV_ILN_2108 | ||
| 912 | |a GBV_ILN_2110 | ||
| 912 | |a GBV_ILN_2111 | ||
| 912 | |a GBV_ILN_2112 | ||
| 912 | |a GBV_ILN_2113 | ||
| 912 | |a GBV_ILN_2116 | ||
| 912 | |a GBV_ILN_2118 | ||
| 912 | |a GBV_ILN_2119 | ||
| 912 | |a GBV_ILN_2122 | ||
| 912 | |a GBV_ILN_2129 | ||
| 912 | |a GBV_ILN_2143 | ||
| 912 | |a GBV_ILN_2144 | ||
| 912 | |a GBV_ILN_2147 | ||
| 912 | |a GBV_ILN_2148 | ||
| 912 | |a GBV_ILN_2152 | ||
| 912 | |a GBV_ILN_2153 | ||
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| 912 | |a GBV_ILN_2336 | ||
| 912 | |a GBV_ILN_2446 | ||
| 912 | |a GBV_ILN_2470 | ||
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| 912 | |a GBV_ILN_4112 | ||
| 912 | |a GBV_ILN_4125 | ||
| 912 | |a GBV_ILN_4126 | ||
| 912 | |a GBV_ILN_4242 | ||
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| 912 | |a GBV_ILN_4249 | ||
| 912 | |a GBV_ILN_4251 | ||
| 912 | |a GBV_ILN_4305 | ||
| 912 | |a GBV_ILN_4306 | ||
| 912 | |a GBV_ILN_4307 | ||
| 912 | |a GBV_ILN_4313 | ||
| 912 | |a GBV_ILN_4322 | ||
| 912 | |a GBV_ILN_4323 | ||
| 912 | |a GBV_ILN_4324 | ||
| 912 | |a GBV_ILN_4325 | ||
| 912 | |a GBV_ILN_4326 | ||
| 912 | |a GBV_ILN_4333 | ||
| 912 | |a GBV_ILN_4334 | ||
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| 912 | |a GBV_ILN_4336 | ||
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| 912 | |a GBV_ILN_4700 | ||
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| 951 | |a AR | ||
| 952 | |d 45 |j 2009 |e 5 |c 05 |h 735-739 | ||
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2009 |
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| allfields |
10.1134/S1070428009050157 doi (DE-627)SPR017483034 (SPR)S1070428009050157-e DE-627 ger DE-627 rakwb eng 540 ASE 35.50 bkl Yunnikova, L. P. verfasserin aut Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Relying on the values of the energy of the highest occupied molecular orbitals calculated ab initio a series of reactivity was established for ylides isomeric to 10-methyl-9,10-dihydroacridine, dibenzopyran, dibenzothiopyran, 1,3-benzodithiol, and the tentative threshold value was determined for imines reaction with the mentioned heterocycles. One- or two-stage imines interaction with 10-methyl-9,10-dihydroacridine or dibenzopyran was confirmed by two reactions of ionic hydroheterylation of N-benzylideneaniline in the presence of sodium tetrahydroborate by the cation of 10-methyl-9,10-dihydroacridinium or the cation of dibenzopyrylium. Xanthene (dpeaa)DE-He213 Sodium Tetrahydroborate (dpeaa)DE-He213 Methyleneaniline (dpeaa)DE-He213 Thioxanthene (dpeaa)DE-He213 Protonated Imine (dpeaa)DE-He213 Makhova, T. V. verfasserin aut Yunnikov, A. L. verfasserin aut Gorokhov, V. Yu. verfasserin aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 45(2009), 5 vom: Mai, Seite 735-739 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:45 year:2009 number:5 month:05 pages:735-739 https://dx.doi.org/10.1134/S1070428009050157 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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 45 2009 5 05 735-739 |
| spelling |
10.1134/S1070428009050157 doi (DE-627)SPR017483034 (SPR)S1070428009050157-e DE-627 ger DE-627 rakwb eng 540 ASE 35.50 bkl Yunnikova, L. P. verfasserin aut Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Relying on the values of the energy of the highest occupied molecular orbitals calculated ab initio a series of reactivity was established for ylides isomeric to 10-methyl-9,10-dihydroacridine, dibenzopyran, dibenzothiopyran, 1,3-benzodithiol, and the tentative threshold value was determined for imines reaction with the mentioned heterocycles. One- or two-stage imines interaction with 10-methyl-9,10-dihydroacridine or dibenzopyran was confirmed by two reactions of ionic hydroheterylation of N-benzylideneaniline in the presence of sodium tetrahydroborate by the cation of 10-methyl-9,10-dihydroacridinium or the cation of dibenzopyrylium. Xanthene (dpeaa)DE-He213 Sodium Tetrahydroborate (dpeaa)DE-He213 Methyleneaniline (dpeaa)DE-He213 Thioxanthene (dpeaa)DE-He213 Protonated Imine (dpeaa)DE-He213 Makhova, T. V. verfasserin aut Yunnikov, A. L. verfasserin aut Gorokhov, V. Yu. verfasserin aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 45(2009), 5 vom: Mai, Seite 735-739 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:45 year:2009 number:5 month:05 pages:735-739 https://dx.doi.org/10.1134/S1070428009050157 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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 45 2009 5 05 735-739 |
| allfields_unstemmed |
10.1134/S1070428009050157 doi (DE-627)SPR017483034 (SPR)S1070428009050157-e DE-627 ger DE-627 rakwb eng 540 ASE 35.50 bkl Yunnikova, L. P. verfasserin aut Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Relying on the values of the energy of the highest occupied molecular orbitals calculated ab initio a series of reactivity was established for ylides isomeric to 10-methyl-9,10-dihydroacridine, dibenzopyran, dibenzothiopyran, 1,3-benzodithiol, and the tentative threshold value was determined for imines reaction with the mentioned heterocycles. One- or two-stage imines interaction with 10-methyl-9,10-dihydroacridine or dibenzopyran was confirmed by two reactions of ionic hydroheterylation of N-benzylideneaniline in the presence of sodium tetrahydroborate by the cation of 10-methyl-9,10-dihydroacridinium or the cation of dibenzopyrylium. Xanthene (dpeaa)DE-He213 Sodium Tetrahydroborate (dpeaa)DE-He213 Methyleneaniline (dpeaa)DE-He213 Thioxanthene (dpeaa)DE-He213 Protonated Imine (dpeaa)DE-He213 Makhova, T. V. verfasserin aut Yunnikov, A. L. verfasserin aut Gorokhov, V. Yu. verfasserin aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 45(2009), 5 vom: Mai, Seite 735-739 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:45 year:2009 number:5 month:05 pages:735-739 https://dx.doi.org/10.1134/S1070428009050157 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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 45 2009 5 05 735-739 |
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10.1134/S1070428009050157 doi (DE-627)SPR017483034 (SPR)S1070428009050157-e DE-627 ger DE-627 rakwb eng 540 ASE 35.50 bkl Yunnikova, L. P. verfasserin aut Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Relying on the values of the energy of the highest occupied molecular orbitals calculated ab initio a series of reactivity was established for ylides isomeric to 10-methyl-9,10-dihydroacridine, dibenzopyran, dibenzothiopyran, 1,3-benzodithiol, and the tentative threshold value was determined for imines reaction with the mentioned heterocycles. One- or two-stage imines interaction with 10-methyl-9,10-dihydroacridine or dibenzopyran was confirmed by two reactions of ionic hydroheterylation of N-benzylideneaniline in the presence of sodium tetrahydroborate by the cation of 10-methyl-9,10-dihydroacridinium or the cation of dibenzopyrylium. Xanthene (dpeaa)DE-He213 Sodium Tetrahydroborate (dpeaa)DE-He213 Methyleneaniline (dpeaa)DE-He213 Thioxanthene (dpeaa)DE-He213 Protonated Imine (dpeaa)DE-He213 Makhova, T. V. verfasserin aut Yunnikov, A. L. verfasserin aut Gorokhov, V. Yu. verfasserin aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 45(2009), 5 vom: Mai, Seite 735-739 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:45 year:2009 number:5 month:05 pages:735-739 https://dx.doi.org/10.1134/S1070428009050157 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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 45 2009 5 05 735-739 |
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10.1134/S1070428009050157 doi (DE-627)SPR017483034 (SPR)S1070428009050157-e DE-627 ger DE-627 rakwb eng 540 ASE 35.50 bkl Yunnikova, L. P. verfasserin aut Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Relying on the values of the energy of the highest occupied molecular orbitals calculated ab initio a series of reactivity was established for ylides isomeric to 10-methyl-9,10-dihydroacridine, dibenzopyran, dibenzothiopyran, 1,3-benzodithiol, and the tentative threshold value was determined for imines reaction with the mentioned heterocycles. One- or two-stage imines interaction with 10-methyl-9,10-dihydroacridine or dibenzopyran was confirmed by two reactions of ionic hydroheterylation of N-benzylideneaniline in the presence of sodium tetrahydroborate by the cation of 10-methyl-9,10-dihydroacridinium or the cation of dibenzopyrylium. Xanthene (dpeaa)DE-He213 Sodium Tetrahydroborate (dpeaa)DE-He213 Methyleneaniline (dpeaa)DE-He213 Thioxanthene (dpeaa)DE-He213 Protonated Imine (dpeaa)DE-He213 Makhova, T. V. verfasserin aut Yunnikov, A. L. verfasserin aut Gorokhov, V. Yu. verfasserin aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 45(2009), 5 vom: Mai, Seite 735-739 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:45 year:2009 number:5 month:05 pages:735-739 https://dx.doi.org/10.1134/S1070428009050157 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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 45 2009 5 05 735-739 |
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Enthalten in Russian journal of organic chemistry 45(2009), 5 vom: Mai, Seite 735-739 volume:45 year:2009 number:5 month:05 pages:735-739 |
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Xanthene Sodium Tetrahydroborate Methyleneaniline Thioxanthene Protonated Imine |
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Russian journal of organic chemistry |
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Yunnikova, L. P. @@aut@@ Makhova, T. V. @@aut@@ Yunnikov, A. L. @@aut@@ Gorokhov, V. Yu. @@aut@@ |
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2009-05-01T00:00:00Z |
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| author |
Yunnikova, L. P. |
| spellingShingle |
Yunnikova, L. P. ddc 540 bkl 35.50 misc Xanthene misc Sodium Tetrahydroborate misc Methyleneaniline misc Thioxanthene misc Protonated Imine Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines |
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540 ASE 35.50 bkl Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines Xanthene (dpeaa)DE-He213 Sodium Tetrahydroborate (dpeaa)DE-He213 Methyleneaniline (dpeaa)DE-He213 Thioxanthene (dpeaa)DE-He213 Protonated Imine (dpeaa)DE-He213 |
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ddc 540 bkl 35.50 misc Xanthene misc Sodium Tetrahydroborate misc Methyleneaniline misc Thioxanthene misc Protonated Imine |
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ddc 540 bkl 35.50 misc Xanthene misc Sodium Tetrahydroborate misc Methyleneaniline misc Thioxanthene misc Protonated Imine |
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ddc 540 bkl 35.50 misc Xanthene misc Sodium Tetrahydroborate misc Methyleneaniline misc Thioxanthene misc Protonated Imine |
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Elektronische Aufsätze Aufsätze Elektronische Ressource |
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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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Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines |
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| title_full |
Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines |
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Yunnikova, L. P. |
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Russian journal of organic chemistry |
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2009 |
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735 |
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Yunnikova, L. P. Makhova, T. V. Yunnikov, A. L. Gorokhov, V. Yu. |
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540 ASE 35.50 bkl |
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Yunnikova, L. P. |
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10.1134/S1070428009050157 |
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540 |
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verfasserin |
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features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines |
| title_auth |
Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines |
| abstract |
Abstract Relying on the values of the energy of the highest occupied molecular orbitals calculated ab initio a series of reactivity was established for ylides isomeric to 10-methyl-9,10-dihydroacridine, dibenzopyran, dibenzothiopyran, 1,3-benzodithiol, and the tentative threshold value was determined for imines reaction with the mentioned heterocycles. One- or two-stage imines interaction with 10-methyl-9,10-dihydroacridine or dibenzopyran was confirmed by two reactions of ionic hydroheterylation of N-benzylideneaniline in the presence of sodium tetrahydroborate by the cation of 10-methyl-9,10-dihydroacridinium or the cation of dibenzopyrylium. |
| abstractGer |
Abstract Relying on the values of the energy of the highest occupied molecular orbitals calculated ab initio a series of reactivity was established for ylides isomeric to 10-methyl-9,10-dihydroacridine, dibenzopyran, dibenzothiopyran, 1,3-benzodithiol, and the tentative threshold value was determined for imines reaction with the mentioned heterocycles. One- or two-stage imines interaction with 10-methyl-9,10-dihydroacridine or dibenzopyran was confirmed by two reactions of ionic hydroheterylation of N-benzylideneaniline in the presence of sodium tetrahydroborate by the cation of 10-methyl-9,10-dihydroacridinium or the cation of dibenzopyrylium. |
| abstract_unstemmed |
Abstract Relying on the values of the energy of the highest occupied molecular orbitals calculated ab initio a series of reactivity was established for ylides isomeric to 10-methyl-9,10-dihydroacridine, dibenzopyran, dibenzothiopyran, 1,3-benzodithiol, and the tentative threshold value was determined for imines reaction with the mentioned heterocycles. One- or two-stage imines interaction with 10-methyl-9,10-dihydroacridine or dibenzopyran was confirmed by two reactions of ionic hydroheterylation of N-benzylideneaniline in the presence of sodium tetrahydroborate by the cation of 10-methyl-9,10-dihydroacridinium or the cation of dibenzopyrylium. |
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5 |
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Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines |
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https://dx.doi.org/10.1134/S1070428009050157 |
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Makhova, T. V. Yunnikov, A. L. Gorokhov, V. Yu |
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Makhova, T. V. Yunnikov, A. L. Gorokhov, V. Yu |
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10.1134/S1070428009050157 |
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2024-07-04T03:31:12.966Z |
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|
| score |
7.4000053 |