Development of Cycloisomerization with Rearrangement of a Tosyl Group Using N-Tosyl-o-allenylaniline
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamada-oka, Suita, Osaka 565-0871, Japan
2. Comprehensive Analysis Centre, SANKEN, Osaka University, Mihogaoka, Ibaraki, Osaka 567-0047, Japan
Funder
Core Research for Evolutional Science and Technology
Japan Agency for Medical Research and Development
Japan Society for the Promotion of Science
Chugai Foundation for Innovative Drug Discovery Science
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c00625
Reference18 articles.
1. Regio‐ and Site‐selective Molecular Rearrangements by Homogeneous Gold Catalysis
2. Synthetic and mechanistic aspects of sulfonyl migrations
3. Highly selective intramolecular addition of C–N and S–N bonds to alkynes catalyzed by palladium: a practical access to two distinct functional indoles
4. Synthesis of Fused Carbazoles by Gold-Catalyzed Tricyclization of Conjugated Diynes via Rearrangement of an N-Propargyl Group
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