has been cited by the following article(s):
[1]
|
Pd-Catalyzed carbonylative lactonization of 2-halidearomatic aldehydes with H2O as a nucleophile
Organic & Biomolecular Chemistry,
2022
DOI:10.1039/D2OB00623E
|
|
|
[2]
|
Recent advancements in synthetic methodologies of 3-substituted phthalides and their application in the total synthesis of biologically active natural products
RSC Advances,
2020
DOI:10.1039/D0RA00701C
|
|
|
[3]
|
Synthesis of New 3-Arylaminophthalides and 3-Indolyl-phthalides using Ammonium Chloride, Evaluation of their Anti-Mycobacterial Potential and Docking Study
Combinatorial Chemistry & High Throughput Screening,
2020
DOI:10.2174/1386207323666200422082754
|
|
|
[4]
|
In-vitro cytotoxicity of synthesized phthalide-fused indoles and indolines against HL-60 and HepG2 cells
Arabian Journal of Chemistry,
2019
DOI:10.1016/j.arabjc.2019.02.002
|
|
|
[5]
|
Solvent-Free Microwave Accelerated Synthesis and Structural Characterization of Phthalide-Fused Indolines
HETEROCYCLES,
2018
DOI:10.3987/COM-17-13796
|
|
|
[6]
|
Iron(III)-Catalyzed 1,3-Functional Group Transposition Reactions: Synthetic Protocol to Access 3-Substituted Indoles
Asian Journal of Organic Chemistry,
2016
DOI:10.1002/ajoc.201600037
|
|
|
[7]
|
Carbazoles from the [4C+2C] Reaction of 2,3-Allenols with Indoles
Chemistry - A European Journal,
2016
DOI:10.1002/chem.201604317
|
|
|
[8]
|
Iron(III)‐Catalyzed 1,3‐Functional Group Transposition Reactions: Synthetic Protocol to Access 3‐Substituted Indoles
Asian Journal of Organic Chemistry,
2016
DOI:10.1002/ajoc.201600037
|
|
|
[9]
|
Carbazoles from the [4C+2C] Reaction of 2,3‐Allenols with Indoles
Chemistry – A European Journal,
2016
DOI:10.1002/chem.201604317
|
|
|
[10]
|
Phthalides and Phthalans: Synthetic Methodologies and Their Applications in the Total Synthesis
Chemical Reviews,
2014
DOI:10.1021/cr400524q
|
|
|
[11]
|
Phthalides and Phthalans: Synthetic Methodologies and Their Applications in the Total Synthesis
Chemical Reviews,
2014
DOI:10.1021/cr400524q
|
|
|