Concise Synthesis of Furo[2,3-b]indolines via [3,3]-Sigmatropic Rearrangement of N-Alkenyloxyindoles
Author:
Affiliation:
1. Department of Chemistry, University of Illinois at Chicago
2. Department of Process Research & Development, Merck & Co., Inc.
Abstract
Funder
National Science Foundation
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0040-1707250.pdf
Reference8 articles.
1. Diversity-Oriented Synthetic Approaches for Furoindoline: A Review
2. Enantiocontrolled total syntheses of (-)-physovenine and (-)-physostigmine
3. Gold-Catalyzed Addition of N-Hydroxy Heterocycles to Alkynes and Subsequent 3,3-Sigmatropic Rearrangement
4. N-Hydroxy indoles as flexible substrates in rearrangements—a novel reaction with activated triple bonds
5. Synthesis of Spirocyclic 1‐Pyrrolines from Nitrones and Arynes through a Dearomative [3,3′]‐Sigmatropic Rearrangement
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