A Rhodium(II)‐Catalyzed Formal [4+1]‐Cycloaddition toward Spirooxindole Pyrrolone Construction Employing Vinyl Isocyanates as 1,4‐Dipoles
Author:
Affiliation:
1. Department of Chemistry and Biochemistry University of Notre Dame Notre Dame IN 46556 USA
Funder
National Science Foundation
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201701147
Reference95 articles.
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2. Cyclopropanes in Organic Synthesis
3. Formal [4+1] Annulation Reactions in the Synthesis of Carbocyclic and Heterocyclic Systems
4. Intramolecular donor–acceptor cyclopropane ring-opening cyclizations
5. Exploitation of Cyclopropane Ring-Cleavage Reactions for the Rapid Assembly of Tetracyclic Frameworks Related to Gibberellins
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1. A Phosphorus(III)‐Mediated (4+1)‐Cycloaddition of 1,2‐Dicarbonyls and Aza‐ o ‐Quinone Methides to Access 2,3‐Dihydroindoles;Helvetica Chimica Acta;2019-12
2. Efficient Synthesis of Spirooxindole Pyrrolones by a Rhodium(III)‐Catalyzed C−H Activation/Carbene Insertion/Lossen Rearrangement Sequence;Angewandte Chemie International Edition;2019-09-16
3. Efficient Synthesis of Spirooxindole Pyrrolones by a Rhodium(III)‐Catalyzed C−H Activation/Carbene Insertion/Lossen Rearrangement Sequence;Angewandte Chemie;2019-08-07
4. Unbridged Rh(ii)–Rh(ii) complexes of N-heterocyclic carbenes and reactions with O2 to form dirhodium(μ–η1:η1-O2) complexes;Dalton Transactions;2019
5. Rhodium-Catalyzed Enantioselective Formal [4+1] Cycloaddition of Diazooxindoles and the Danishefsky Diene;Asian Journal of Organic Chemistry;2018-01-19
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