Transition-Metal-Free Tunable Chemoselective N Functionalization of Indoles with Ynamides
Author:
Publisher
Wiley
Subject
General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.201402767/fullpdf
Reference65 articles.
1. Ynamides in Ring Forming Transformations
2. Inamide: vielseitige Bausteine für die organische Synthese
3. Ynamides: Versatile Tools in Organic Synthesis
4. Ynamides: A Modern Functional Group for the New Millennium
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1. Base‐Mediated Generation of Ketenimines from Ynamides: Addition of Hydrazones to Give Acetimidohydrazides**;European Journal of Organic Chemistry;2022-05-12
2. Quadruple Functionalization of a Tetraphenylethylene Aromatic Scaffold with Ynamides or Tetracyanobutadienes: Synthesis and Optical Properties;European Journal of Organic Chemistry;2022-03-24
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4. Media‐Driven Pd‐Catalyzed Reaction Cascades with 1,3‐Diynamides Leading Selectively to Either Indoles or Quinolines;Angewandte Chemie;2021-09-13
5. Azetidinimines as a novel series of non-covalent broad-spectrum inhibitors of β-lactamases with submicromolar activities against carbapenemases KPC-2 (class A), NDM-1 (class B) and OXA-48 (class D);European Journal of Medicinal Chemistry;2021-07
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