Gold(I)-Catalyzed Dearomative Rautenstrauch Rearrangement: Enantioselective Access to Cyclopenta[b]indoles
Author:
Affiliation:
1. Department of Chemistry, University of California, Berkeley, California 94720, United States
2. Institute of Chemistry and BioMedical Sciences, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210046, P. R. China
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.5b00613
Reference61 articles.
1. 2-Cyclopentenones from 1-ethynyl-2-propenyl acetates
2. Palladium(II)- and mercury(II)-catalyzed rearrangements of propargyl acetates
3. Pt-Catalyzed Pentannulations from In Situ Generated Metallo−Carbenoids Utilizing Propargylic Esters
4. Regiodivergent Synthesis of Functionalized Indene Derivatives via Pt-Catalyzed Rautenstrauch Reaction of Propargyl Carbonates
5. Transition metal-catalyzed pentannulation of propargyl acetates via styrylcarbene intermediates
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