Synthesis of Unsymmetrical 3,3′-Dialkyloxindole Boronic Esters from 3-Alkylidene-2-oxindoles Enabled by Copper Catalysis-Reference-Cited by-同舟云学术

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Synthesis of Unsymmetrical 3,3′-Dialkyloxindole Boronic Esters from 3-Alkylidene-2-oxindoles Enabled by Copper Catalysis

Published:2024-07-06 Issue:14 Volume:89 Page:10403-10408
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Mondal Pinku Prasad¹,Chungath Alvin Antony¹,Krishnan Malavika¹,Das Subham¹,Mandodi Aarya¹,Sahoo Basudev¹^ORCID

Affiliation:

1. School of Chemistry, Indian Institute of Science Education and Research Thiruvananthapuram, Thiruvananthapuram 695551, Kerala, India

Funder

Science and Engineering Research Board

Ministry of Education, India

Indian Institute of Science Education and Research Thiruvananthapuram

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c01326

Reference42 articles.

1. Oxindole and its derivatives: A review on recent progress in biological activities

2. 3‐Alkenyl‐oxindoles: Natural Products, Pharmaceuticals, and Recent Synthetic Advances in Tandem/Telescoped Approaches

3. Catalytic Asymmetric Ring-Opening/Cyclopropanation of Cyclic Sulfur Ylides: Construction of Sulfur-Containing Spirocyclopropyloxindoles with Three Vicinal Stereocenters

4. Metal-free intermolecular cyclopropanation between alkenes and iodonium ylides mediated by PhI(OAc)2·Bu4NI

5. Enantioselective 1,3-Dipolar Cycloaddition of Methyleneindolinones with α-Diazomethylphosphonate to Access Chiral Spiro-phosphonylpyrazoline-oxindoles Catalyzed by Tertiary Amine Thiourea and 1,5-Diazabicyclo[4.3.0]non-5-ene

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