✦ LIBER ✦

Tunable Hydride Transfer in the Redox Amination of Indoline with Aldehyde: An Attractive Intramolecular Hydrogen-Bond Effect

✍ Scribed by Hui Mao; Runsheng Xu; Dr. Jieping Wan; Zhengyang Jiang; Prof. Dr. Cuirong Sun; Prof. Dr. Yuanjiang Pan

Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 174 KB
Volume: 16
Category: Article
ISSN: 0947-6539
DOI: 10.1002/chem.201001896

No coin nor oath required. For personal study only.

✦ Synopsis

Supporting information for this article is available on the WWW under http://dx.doi.org/10.1002/chem.201001896. Scheme 1. A proposed hypothesis for the formation of N-benzylindole 3 a.

📜 SIMILAR VOLUMES

ChemInform Abstract: Tunable Hydride Tra

ChemInform Abstract: Tunable Hydride Transfer in the Redox Amination of Indoline with Aldehyde: An Attractive Intramolecular Hydrogen-Bond Effect.

✍ Hui Mao; Runsheng Xu; Jieping Wan; Zhengyang Jiang; Cuirong Sun; Yuanjiang Pan 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

## Abstract A Broensted acid catalyzed redox amination of indoline with aldehydes for the synthesis of N‐alkylindoles (III) proceeds via intramolecular hydride transfer.