1,3-Dipolar cycloaddition reactions of isatin-derived azomethine ylides for the synthesis of spirooxindole and indole-derived scaffolds: recent developments-Reference-Cited by-同舟云学术

1,3-Dipolar cycloaddition reactions of isatin-derived azomethine ylides for the synthesis of spirooxindole and indole-derived scaffolds: recent developments

Published:2022-08-04 Issue: Volume: Page:
ISSN:1381-1991
Container-title:Molecular Diversity
language:en
Short-container-title:Mol Divers

Author:

Miankooshki Fatemeh Rostami,Bayat Mohammad^ORCID,Nasri Shima,Samet Narges Habibi

Publisher

Springer Science and Business Media LLC

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Molecular Biology,General Medicine,Information Systems,Catalysis

Link

https://link.springer.com/content/pdf/10.1007/s11030-022-10510-9.pdf

Reference81 articles.

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2. Kidd SL, Osberger TJ, Mateu N, Sore HF, Spring DR (2018) Recent applications of diversity-oriented synthesis toward novel, 3-dimensional fragment collections. Front Chem 6:460. https://doi.org/10.3389/fchem.2018.00460

3. Chen Y, Cui BD, Wang Y, Han WY, Wan NW, Bai M, Chen YZ (2018) Asymmetric [3+2] cycloaddition reaction of isatin-derived MBH carbonates with 3-methyleneoxindoles: enantioselective synthesis of 3,3′-cyclopentenyldispirooxindoles incorporating two adjacent quaternary spirostereocenters. J Org Chem 83:10465–10475. https://doi.org/10.1021/acs.joc.8b01506

4. Adrio J, Carretero JC (2014) Recent advances in the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides. Chem Commun 50:12434–12446. https://doi.org/10.1039/C4CC04381B

5. Shiri P (2021) Novel hybrid molecules based on triazole-β-lactam as potential biological agents. Mini-Rev Med Chem 21:536–553. https://doi.org/10.2174/1389557520666201027160436

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