Profiles
Research Units
Publications
Sign Up
Faculty Login
X
Articles
Facile formation of cyclic aminals through a Brønsted acid-promoted redox process
C. Zhang
,
Sandip Murarka
,
D. Seidel
Published in
2009
DOI:
10.1021/jo802325x
PMID:
19053590
Volume: 74
Issue: 1
Pages: 419 - 422
Abstract
(Chemical Equation Presented) Cyclic aminals were prepared through a Brønsted acid-promoted reaction. This redox neutral process involves iminium ion formation, 1,5 H-transfer, followed by ring closure. © 2009 American Chemical Society.
Request full-text
Cite
Content may be subject to copyright.
Journal Details
Authors (1)
About the journal
Journal
Journal of Organic Chemistry
ISSN
00223263
Authors (1)
Sandip Murarka
Department of Chemistry
IIT Jodhpur
Recent publications
Organophotoredox-Catalyzed Late-Stage Functionalization of Heterocycles
Hypervalent iodine(III) reagents in the synthesis of heterocyclic compounds
Metal-Catalyzed Oxidative Coupling of Ketones and Ketone Enolates
Catalytic enantioselective intramolecular redox reactions: Ring-fused tetrahydroquinolines
Get all the updates for this publication
Follow