Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines
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 imi...
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| Veröffentlicht in: | Russian journal of organic chemistry 2009-05, Vol.45 (5), p.735-739 |
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| container_title | Russian journal of organic chemistry |
| container_volume | 45 |
| creator | Yunnikova, L. P. Makhova, T. V. Yunnikov, A. L. Gorokhov, V. Yu |
| description | 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. |
| doi_str_mv | 10.1134/S1070428009050157 |
| format | Article |
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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.</description><identifier>ISSN: 1070-4280</identifier><identifier>EISSN: 1608-3393</identifier><identifier>DOI: 10.1134/S1070428009050157</identifier><language>eng</language><publisher>Dordrecht: SP MAIK Nauka/Interperiodica</publisher><subject>Chemistry ; Chemistry and Materials Science ; Organic Chemistry</subject><ispartof>Russian journal of organic chemistry, 2009-05, Vol.45 (5), p.735-739</ispartof><rights>Pleiades Publishing, Ltd. 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c288t-2f507b63b06b152106753c21c83c891bc6976200e1e08baa1116136a91b9f3723</citedby><cites>FETCH-LOGICAL-c288t-2f507b63b06b152106753c21c83c891bc6976200e1e08baa1116136a91b9f3723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S1070428009050157$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1070428009050157$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,782,786,27931,27932,41495,42564,51326</link.rule.ids></links><search><creatorcontrib>Yunnikova, L. 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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.</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Organic Chemistry</subject><issn>1070-4280</issn><issn>1608-3393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kEFLxDAQhYMouK7-AG_9AUZnkjZNjrK4KiyIqOeSpuk2S9tI0kX678263gRP8x7fvIF5hFwj3CLy_O4NoYScSQAFBWBRnpAFCpCUc8VPk06YHvg5uYhxBwA55nxBXtdWT_tgY-bbLFhtJufHH4NABzt1c0_VTdKN6-YmeG2Ca9xos85ONtlR934bsy83dZkbEoiX5KzVfbRXv3NJPtYP76snunl5fF7db6hhUk6UtQWUteA1iBoLhiDKghuGRnIjFdZGqFIwAIsWZK01IgrkQiekWl4yviR4vGuCjzHYtvoMbtBhrhCqQyfVn05Shh0zMe2OWxuqnd-H9EP8J_QNdcphgQ</recordid><startdate>20090501</startdate><enddate>20090501</enddate><creator>Yunnikova, L. 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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><cop>Dordrecht</cop><pub>SP MAIK Nauka/Interperiodica</pub><doi>10.1134/S1070428009050157</doi><tpages>5</tpages></addata></record> |
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| ispartof | Russian journal of organic chemistry, 2009-05, Vol.45 (5), p.735-739 |
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| language | eng |
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| source | SpringerNature Journals |
| subjects | Chemistry Chemistry and Materials Science Organic Chemistry |
| title | Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines |
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