A new synthetic approach to pentacyclic ring, 6,7,14,15-tetrahydro[1,5] diazocino[1,2-a:6,5-a']-8-dihydrodiindole
The construction of a new pentacyclic ring system, 6,7,14,15-tetrahydro[1, 5]diazocino[1,2-a:6,5-a'] -8-dihydrodiindole (7) from simple precursors through our new synthetic route was presented to be a facile and concise method for an intramolecular N-alkylation of tosylate 12 which was obtained...
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th-mahidol.116892018-05-03T15:41:14Z A new synthetic approach to pentacyclic ring, 6,7,14,15-tetrahydro[1,5] diazocino[1,2-a:6,5-a']-8-dihydrodiindole Kittisak Sripha Darius Paul Zlotos Ulrike Holzgrabe Somsak Ruchirawat Mahidol University Julius-Maximilians-Universitat Wurzburg Chulabhorn Research Institute Chemistry Pharmacology, Toxicology and Pharmaceutics The construction of a new pentacyclic ring system, 6,7,14,15-tetrahydro[1, 5]diazocino[1,2-a:6,5-a'] -8-dihydrodiindole (7) from simple precursors through our new synthetic route was presented to be a facile and concise method for an intramolecular N-alkylation of tosylate 12 which was obtained from N-acylation of indoline 4 with indole acid 9, followed by reduction and tosylation. This new synthetic approach can overcome the disadvantage of uncontrollable intermolecular double N-alkylation of the precursor 3 to produce the unexpected ring system 2. © 2011 The Japan Institute of Heterocyclic Chemistry. 2018-05-03T08:06:30Z 2018-05-03T08:06:30Z 2011-10-31 Article Heterocycles. Vol.83, No.11 (2011), 2627-2633 10.3987/COM-11-12340 18810942 03855414 2-s2.0-80455125913 https://repository.li.mahidol.ac.th/handle/123456789/11689 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=80455125913&origin=inward |
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Chemistry Pharmacology, Toxicology and Pharmaceutics Kittisak Sripha Darius Paul Zlotos Ulrike Holzgrabe Somsak Ruchirawat A new synthetic approach to pentacyclic ring, 6,7,14,15-tetrahydro[1,5] diazocino[1,2-a:6,5-a']-8-dihydrodiindole |
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The construction of a new pentacyclic ring system, 6,7,14,15-tetrahydro[1, 5]diazocino[1,2-a:6,5-a'] -8-dihydrodiindole (7) from simple precursors through our new synthetic route was presented to be a facile and concise method for an intramolecular N-alkylation of tosylate 12 which was obtained from N-acylation of indoline 4 with indole acid 9, followed by reduction and tosylation. This new synthetic approach can overcome the disadvantage of uncontrollable intermolecular double N-alkylation of the precursor 3 to produce the unexpected ring system 2. © 2011 The Japan Institute of Heterocyclic Chemistry. |
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Mahidol University |
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Mahidol University Kittisak Sripha Darius Paul Zlotos Ulrike Holzgrabe Somsak Ruchirawat |
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Kittisak Sripha Darius Paul Zlotos Ulrike Holzgrabe Somsak Ruchirawat |
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Kittisak Sripha |
title |
A new synthetic approach to pentacyclic ring, 6,7,14,15-tetrahydro[1,5] diazocino[1,2-a:6,5-a']-8-dihydrodiindole |
title_short |
A new synthetic approach to pentacyclic ring, 6,7,14,15-tetrahydro[1,5] diazocino[1,2-a:6,5-a']-8-dihydrodiindole |
title_full |
A new synthetic approach to pentacyclic ring, 6,7,14,15-tetrahydro[1,5] diazocino[1,2-a:6,5-a']-8-dihydrodiindole |
title_fullStr |
A new synthetic approach to pentacyclic ring, 6,7,14,15-tetrahydro[1,5] diazocino[1,2-a:6,5-a']-8-dihydrodiindole |
title_full_unstemmed |
A new synthetic approach to pentacyclic ring, 6,7,14,15-tetrahydro[1,5] diazocino[1,2-a:6,5-a']-8-dihydrodiindole |
title_sort |
new synthetic approach to pentacyclic ring, 6,7,14,15-tetrahydro[1,5] diazocino[1,2-a:6,5-a']-8-dihydrodiindole |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/11689 |
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1763487799400464384 |