Phenyliodine(III)diacetate (PIDA): Applications in Organic Synthesis
Abstract
:1. Introduction
2. Recent Applications of PIDA (from 2015)
2.1. C-H Functionalization and Hetero-Hetero Bond Formations
2.1.1. C-C Bond Formation
- (a)
- C-Alkylation reaction
- (b)
- C-C bond formation reaction on alkenes
2.1.2. C-O and C-X Bond Formation
2.1.3. C-N Bond Formation
2.1.4. C-Se Bond Formation
2.1.5. Hetero-Hetero Bond Formation
2.2. Heterocyclic Ring Formations
2.2.1. Synthesis of Oxazoline and Thiazoline Derivatives
2.2.2. Synthesis of Quinoxaline Derivatives
2.2.3. Synthesis of Imidazolidinones
2.3. Rearrangement/Migration Reactions
2.3.1. Hetero Diels-Alder Addition
2.3.2. Beckmann-Type Rearrangement
2.3.3. Hofmann Rearrangement
2.3.4. Morin Rearrangement
2.3.5. Grob-Type Fragmentation
2.3.6. 1,2-Diaza-Cope Rearrangement
2.4. Miscellaneous Reactions
2.4.1. Synthesis of Aryl(trifloxyalkenyl)iodonium Triflate Salts
2.4.2. Dearomative Spirocyclization
2.4.3. Generation of α-Aminoalkyl Radicals
2.4.4. Ring Opening Reaction
2.4.5. Oxidative Cleavage of C2–C3 Bond
2.4.6. Oxidation
2.4.7. Synthesis of Furylpyrazolino[60]fullerene Derivatives
2.4.8. Catalytic Oxidation of Styrene
2.4.9. Synthesis of 1,4-Bridged Dihydroisoquinolin-3-Ones
2.4.10. Regioselective Synthesis of 1-(Benzoxazol-2-yl)-1-Alkoxynaphthalen-2(1H)-Ones
2.4.11. Synthesis of Acylated Benzimidazo/Indolo[2,1-a]isoquinolines
2.4.12. Oxidative Dearomatization
3. Conclusions
Author Contributions
Funding
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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Varala, R.; Seema, V.; Dubasi, N. Phenyliodine(III)diacetate (PIDA): Applications in Organic Synthesis. Organics 2023, 4, 1-40. https://doi.org/10.3390/org4010001
Varala R, Seema V, Dubasi N. Phenyliodine(III)diacetate (PIDA): Applications in Organic Synthesis. Organics. 2023; 4(1):1-40. https://doi.org/10.3390/org4010001
Chicago/Turabian StyleVarala, Ravi, Vittal Seema, and Narsimhaswamy Dubasi. 2023. "Phenyliodine(III)diacetate (PIDA): Applications in Organic Synthesis" Organics 4, no. 1: 1-40. https://doi.org/10.3390/org4010001