✦ LIBER ✦

I 2 /TBHP-Catalyzed Chemoselective Amination of Indoles

✍ Scribed by Cai, Zhong-Jian; Wang, Shun-Yi; Ji, Shun-Jun

Book ID: 121190763
Publisher: American Chemical Society
Year: 2013
Tongue: English
Weight: 289 KB
Volume: 15
Category: Article
ISSN: 1523-7060
DOI: 10.1021/ol4023936

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of Isatins by I 2 /TBHP Mediat

Synthesis of Isatins by I 2 /TBHP Mediated Oxidation of Indoles

✍ Zi, You; Cai, Zhong-Jian; Wang, Shun-Yi; Ji, Shun-Jun 📂 Article 📅 2014 🏛 American Chemical Society 🌐 English ⚖ 713 KB

Synthesis of Pyrazolo[1,5-a]indoles via

Synthesis of Pyrazolo[1,5-a]indoles via Copper(I)-Catalyzed Intramolecular Amination.

✍ Yong-Ming Zhu; Lie-Na Qin; Rui Liu; Shun-Jun Ji; Hajime Katayama 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

Palladium-/Copper-Catalyzed Regioselecti

Palladium-/Copper-Catalyzed Regioselective Amination and Chloroamination of Indoles

✍ Liu, Xue-Yuan; Gao, Pin; Shen, Yong-Wen; Liang, Yong-Min 📂 Article 📅 2011 🏛 American Chemical Society 🌐 English ⚖ 779 KB

Recyclable Ru/C catalyzed oxidative cyan

Recyclable Ru/C catalyzed oxidative cyanation of tertiary amines with TBHP

✍ Reddy, K. Harsha Vardhan; Satish, G.; Reddy, V. Prakash; Kumar, B. S. P. Anil; N 📂 Article 📅 2012 🏛 The Royal Society of Chemistry 🌐 English ⚖ 420 KB

Silica-supported ceric ammonium nitrate

Silica-supported ceric ammonium nitrate catalyzed chemoselective formylation of indoles

✍ Tongkhan, Sukanya; Radchatawedchakoon, Widchaya; Kruanetr, Senee; Sakee, Uthai 📂 Article 📅 2014 🏛 Elsevier Science 🌐 French ⚖ 315 KB

Hydrogen bond catalyzed chemoselective N

Hydrogen bond catalyzed chemoselective N-tert-butoxycarbonylation of amines

✍ Samad Khaksar; Akbar Heydari; Mahmood Tajbakhsh; Seyed Mohammad Vahdat 📂 Article 📅 2008 🏛 Elsevier Science 🌐 French ⚖ 135 KB

A novel, chemoselective mono-N-Boc protection of various structurally diverse amines with di-tert-butoxypyrocarbonate (Boc) 2 O is described that relies on selective carbonyl activation by hydrogen bond formation. This mild, acid-and metal-free process requires only catalytic amounts of thiourea as