A simple route to γ-carbolines and indolizino[7, 6-b]indoles. Issue 46 (18th November 2015)
- Record Type:
- Journal Article
- Title:
- A simple route to γ-carbolines and indolizino[7, 6-b]indoles. Issue 46 (18th November 2015)
- Main Title:
- A simple route to γ-carbolines and indolizino[7, 6-b]indoles
- Authors:
- Pilipenko, Arkady S.
Uchuskin, Maxim G.
Trushkov, Igor V.
Butin, Alexander V. - Abstract:
- Abstract: We designed and realized for the first time an approach to indolizino[7, 6- b ]indoles. This approach is based on the Leuckart–Wallach reaction of 2-(2-oxoalkyl)indoles with formamide followed by Bischler–Napieralski cyclization producing γ-carbolines. The alkylation of 3-alkyl-γ-carbolines with phenacyl bromides followed by the treatment of the formed pyridinium salt with base produced the target aromatic tetracyclic system. Graphical abstract:
- Is Part Of:
- Tetrahedron. Volume 71:Issue 46(2015)
- Journal:
- Tetrahedron
- Issue:
- Volume 71:Issue 46(2015)
- Issue Display:
- Volume 71, Issue 46 (2015)
- Year:
- 2015
- Volume:
- 71
- Issue:
- 46
- Issue Sort Value:
- 2015-0071-0046-0000
- Page Start:
- 8786
- Page End:
- 8790
- Publication Date:
- 2015-11-18
- Subjects:
- Indoles -- Reductive amination -- Bischler–Napieralski cyclization -- γ-Carbolines -- Indolizino[7, 6-b]indoles
Chemistry, Organic -- Periodicals
547.005 - Journal URLs:
- http://www.elsevier.com/journals ↗
- DOI:
- 10.1016/j.tet.2015.09.046 ↗
- Languages:
- English
- ISSNs:
- 0040-4020
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8796.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 438.xml