ChemInform Abstract: Facile Synthesis of Indolizino[3, 4, 5‐ab]isoindoles by an Acid‐Induced Cyclization of 1, 2‐Di(1H‐pyrrol‐2‐yl)benzenes. Issue 2 (23rd December 2015)

Record Type:: Journal Article
Title:: ChemInform Abstract: Facile Synthesis of Indolizino[3, 4, 5‐ab]isoindoles by an Acid‐Induced Cyclization of 1, 2‐Di(1H‐pyrrol‐2‐yl)benzenes. Issue 2 (23rd December 2015)
Main Title:: ChemInform Abstract: Facile Synthesis of Indolizino[3, 4, 5‐ab]isoindoles by an Acid‐Induced Cyclization of 1, 2‐Di(1H‐pyrrol‐2‐yl)benzenes.
Authors:: Kuzuhara, Daiki
Miyake, Satoshi
Moriyama, Hirotake
Tamura, Yuto
Aratani, Naoki
Yamada, Hiroko
Abstract:: Abstract: The two‐step synthesis of the substrates via Suzuki‐coupling of the corresponding 1, 2‐dibromobenzene with N‐Boc‐pyrrole‐2‐boronic acid and subsequent N‐deprotection is described.
Is Part Of:: ChemInform. Volume 47:Issue 2(2016)
Journal:: ChemInform
Issue:: Volume 47:Issue 2(2016)
Issue Display:: Volume 47, Issue 2 (2016)
Year:: 2016
Volume:: 47
Issue:: 2
Issue Sort Value:: 2016-0047-0002-0000
Page Start:: no
Page End:: no
Publication Date:: 2015-12-23
Subjects:: fused pyrrole derivatives -- ring closure reactions, annulation reactions -- optical properties (excluding spectra) (organic substances)
Chemistry -- Abstracts -- Periodicals
540.5
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1522-2667 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/chin.201602115 ↗
Languages:: English
ISSNs:: 0931-7597
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3158.195000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 787.xml