ChemInform Abstract: 3‐Alkenyl‐2‐silyloxyindoles in Vinylogous Mannich Reactions: Synthesis of Aminated Indole‐Based Scaffolds and Products. Issue 29 (22nd July 2014)

Record Type:: Journal Article
Title:: ChemInform Abstract: 3‐Alkenyl‐2‐silyloxyindoles in Vinylogous Mannich Reactions: Synthesis of Aminated Indole‐Based Scaffolds and Products. Issue 29 (22nd July 2014)
Main Title:: ChemInform Abstract: 3‐Alkenyl‐2‐silyloxyindoles in Vinylogous Mannich Reactions: Synthesis of Aminated Indole‐Based Scaffolds and Products.
Authors:: Ranieri, Beatrice
Sartori, Andrea
Curti, Claudio
Battistini, Lucia
Rassu, Gloria
Pelosi, Giorgio
Casiraghi, Giovanni
Zanardi, Franca
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Tbs‐Protected oxydienes, derived from enolizable alkylideneoxindoles, serve as extended carbon nucleophiles in Lewis acid‐catalyzed vinylogous Mukaiyama‐type Mannich coupling with both aliphatic and aromatic N‐Boc aminals.</p> </abstract>
Is Part Of:: ChemInform. Volume 45:Issue 29(2014)
Journal:: ChemInform
Issue:: Volume 45:Issue 29(2014)
Issue Display:: Volume 45, Issue 29 (2014)
Year:: 2014
Volume:: 45
Issue:: 29
Issue Sort Value:: 2014-0045-0029-0000
Page Start:: no
Page End:: no
Publication Date:: 2014-07-22
Subjects:: 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.201429135 ↗
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:: 3102.xml