Iodine(III)‐Mediated Unexpected Ring‐Contraction Rearrangement and Halogenated Addition Reaction to Synthesize 3‐Substituted Phthalides and Isochroman‐1‐One Derivatives

Abstract Iodine(III)‐mediated ring‐contraction rearrangement and halogenated addition reaction have been realized. A series of 3‐substituted phthalides and isochroman‐1‐one derivatives bearing multiple functional groups were obtained in good to excellent yields under mild reaction conditions. Computational studies indicated that the reaction proceeds via a proton transfer followed by ring opening and ring formation to produce the target product. Moreover, preliminary biological evaluations revealed that both of 3‐substituted phthalides and isochroman‐1‐one derivatives show good antitumor activities.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-12-12
DOI
https://doi.org/10.1002/ejoc.202401173
Citations
1
Primary Topic
Synthesis and pharmacology of benzodiazepine derivatives
Type
article
Field-Weighted Citation Impact
0.25
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article

Iodine(III)‐Mediated Unexpected Ring‐Contraction Rearrangement and Halogenated Addition Reaction to Synthesize 3‐Substituted Phthalides and Isochroman‐1‐One Derivatives

Tao Liu, Xinxin Si, Yang Cao, Wenhui Cui et al.
1 citations
European Journal of Organic Chemistry
Synthesis and pharmacology of benzodiazepine derivatives
0.25
article

Iodine(III)‐Mediated Unexpected Ring‐Contraction Rearrangement and Halogenated Addition Reaction to Synthesize 3‐Substituted Phthalides and Isochroman‐1‐One Derivatives

Tao Liu, Xinxin Si, Yang Cao, Wenhui Cui, Yihang Zhou, Fanjing Meng
article en
1 citations

Abstract

Abstract Iodine(III)‐mediated ring‐contraction rearrangement and halogenated addition reaction have been realized. A series of 3‐substituted phthalides and isochroman‐1‐one derivatives bearing multiple functional groups were obtained in good to excellent yields under mild reaction conditions. Computational studies indicated that the reaction proceeds via a proton transfer followed by ring opening and ring formation to produce the target product. Moreover, preliminary biological evaluations revealed that both of 3‐substituted phthalides and isochroman‐1‐one derivatives show good antitumor activities.

European Journal of Organic ChemistryVol. 28(4)
Qufu Normal University (CN), Kanion Pharmaceutical (China) (CN), Jining University (CN), College of Marin (US), Nanjing University (CN)
Openalex Percentile: Top 46%
Synthesis and pharmacology of benzodiazepine derivatives
0.25
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