One-Pot Reaction between N-Tosylhydrazones and 2-Nitrobenzyl Bromide: Route to NH-Free C2-Arylindoles-Reference-Cited by-同舟云学术

One-Pot Reaction between N-Tosylhydrazones and 2-Nitrobenzyl Bromide: Route to NH-Free C2-Arylindoles

Published:2018-12-07 Issue:1 Volume:84 Page:228-238
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bzeih Tourin¹²,Zhang Kena¹,Khalaf Ali²,Hachem Ali²,Alami Mouad¹,Hamze Abdallah¹^ORCID

Affiliation:

1. LabEx LERMIT, Laboratoire de Chimie Thérapeutique, Faculté de Pharmacie, Université Paris-Sud, CNRS, BioCIS−UMR 8076, rue J.-B. Clément, Châtenay-Malabry F−92296, France

2. Laboratory for Medicinal Chemistry and Natural Products, Faculty of Sciences (1), and PRASE-EDST, Lebanese University, Hadath, Lebanon

Funder

Ligue Contre le Cancer

Centre National de la Recherche Scientifique

Universit? Paris-Sud

China Scholarship Council

Universit? Libanaise

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b02623

Reference65 articles.

1. N-Tosylhydrazones: versatile synthons in the construction of cyclic compounds

2. Tosylhydrazones: New Uses for Classic Reagents in Palladium-Catalyzed Cross-Coupling and Metal-Free Reactions

3. Copper-catalyzed reductive coupling of tosylhydrazones with amines: A convenient route to α-branched amines

4. Copper Acetoacetonate [Cu(acac)2]/BINAP-Promoted Csp3N Bond FormationviaReductive Coupling ofN-Tosylhydrazones with Anilines

5. Straightforward Synthesis of Ethers: Metal-Free Reductive Coupling of Tosylhydrazones with Alcohols or Phenols

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