3-Methyleneisoindolin-1-one Assembly via Base- and CuI/l-Proline-Catalyzed Domino Reaction: Mechanism of Regioselective Anionic Cyclization
Author:
Affiliation:
1. Shimadzu Institute for Research Technology, University of Texas at Arlington, Arlington, Texas 76019, United States
2. Department of Chemistry and Biochemistry, Texas Christian University, Fort Worth, Texas 76129, United States
Funder
Texas Christian University
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b01904
Reference32 articles.
1. Regio- and Stereoselective Synthesis of Isoindolin-1-ones via Electrophilic Cyclization
2. Copper-Mediated Tandem Oxidative C(sp2)–H/C(sp)–H Alkynylation and Annulation of Arenes with Terminal Alkynes
3. Palladium-Catalysed Heteroannulation with Terminal Alkynes: a Highly Regio- and Stereoselective Synthesis of (Z)-3-Aryl(alkyl)idene Isoindolin-1-ones
4. Tuning Selectivity of Anionic Cyclizations: Competition between 5-Exo and 6-Endo-Dig Closures of Hydrazides of o-Acetylenyl Benzoic Acids and Based-Catalyzed Fragmentation/Recyclization of the Initial 5-Exo-Dig Products
5. Synthesis of Extended, π-Conjugated Isoindolin-1-ones
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