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1. Full Text Tandem Catalytic C(sp3)H Amination/Sila‐Sonogashira–Hagihara Coupling Reactions with Iodine Reagents
by Buendia, Julien and Darses, Benjamin and Dauban, Philippe
Angewandte Chemie International Edition, ISSN 1433-7851, 05/2015, Volume 54, Issue 19, pp. 5697 - 5701
A new tandem CN and CC bond‐forming reaction has been achieved through RhII/Pd0 catalysis. The sequence first involves an iodine(III) oxidant, then the in... 
homogeneous catalysis | cross‐coupling | hypervalent compounds | synthetic methods | CH Activation | cross-coupling | C-H Activation | PALLADIUM | CASCADE REACTIONS | ALKYNYLSILANES | MEDIATED AZIRIDINATION | DIARYLIODONIUM SALTS | CHEMISTRY, MULTIDISCIPLINARY | FUNCTIONALIZATION | CHEMISTRY | ARYL IODIDES | STEREOSELECTIVE-SYNTHESIS | C-H AMINATION | Iodine | Oxidants | Oxidizing agents | Byproducts | Joining | Oxidation | Catalysis | Bonding | Bonding agents | Chemical Sciences
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2. Full Text Hypervalent iodine chemistry
: preparation, structure and synthetic applications of polyvalent iodine compounds
by Zhdankin, Viktor V
2013, 1st ed., ISBN 1118341317, 480
Hypervalent Iodine Chemistry is the first comprehensive text covering all of the main aspects of the chemistry of organic and inorganic polyvalent iodine... 
Hypervalence (Theoretical chemistry) | Iodine compounds | Chemistry | SCIENCE | Organoiodine compounds | Organic
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3. Full Text Sunlight‐Driven Decarboxylative Alkynylation of α‐Keto Acids with Bromoacetylenes by Hypervalent Iodine Reagent Catalysis: A Facile Approach to Ynones
by Tan, Hui and Li, Hongji and Ji, Wangqin and Wang, Lei
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2015, Volume 54, Issue 29, pp. 8374 - 8377
A novel and practical decarboxylative alkynylation of α‐keto acids with bromoacetylenes is catalyzed by hypervalent iodine(III) reagents when irradiation by... 
radicals | photochemistry | acylation | hypervalent compounds | alkynes | OXIDATION | ROOM-TEMPERATURE | ARYLATION | OXOCARBOXYLIC ACIDS | TERMINAL ALKYNES | C-H ACTIVATION | CHEMISTRY, MULTIDISCIPLINARY | PHOTOREDOX CATALYSIS | ORTHO-ACYLATION | ACCESS | CARBOXYLIC-ACIDS | Iodine - chemistry | Acetylene - chemistry | Ketones - chemical synthesis | Decarboxylation | Keto Acids - chemistry | Halogenation | Ketones - chemistry | Sunlight | Alkynes - chemistry | Catalysis | Acylation | Irradiation | Sun | Radicals | Iodine
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4. Full Text Hypervalent Iodine Goes Catalytic
by Richardson, Robert D and Wirth, Thomas
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2006, Volume 45, Issue 27, pp. 4402 - 4404
A dash of iodine: Different reactions relying on the power of hypervalent iodine reagents can now be performed with catalytic amounts of these compounds and a... 
oxidation | catalysis | iodine | hypervalent compounds | synthetic methods | Oxidation | Synthetic methods | Catalysis | Hypervalent compounds | Iodine | REACTIVITY | CARBONYL-COMPOUNDS | IN-SITU GENERATION | CHEMISTRY, MULTIDISCIPLINARY | ALCOHOLS | M-CHLOROPERBENZOIC ACID | KETONES | TRANSITION-METAL-FREE | IBX | DIRECTIONS
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5. Full Text An Efficient Palladium‐Catalyzed CH Alkoxylation of Unactivated Methylene and Methyl Groups with Cyclic Hypervalent Iodine (I3+) Oxidants
by Shan, Gang and Yang, Xinglin and Zong, Yu and Rao, Yu
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2013, Volume 52, Issue 51, pp. 13606 - 13610
All the hype: The title reaction has been developed for the facile synthesis of a variety of complex alkyl ethers. Cyclic hypervalent iodine (I3+) reagents... 
oxidation | CH activation | palladium | iodine | hypervalent compounds | C-H activation | ORGANIC-MOLECULES | ACTIVATION | ARYLATION | BOND FORMATION | CHEMISTRY, MULTIDISCIPLINARY | FUNCTIONALIZATION | CROSS-COUPLING REACTIONS | CH activation | CONSTRUCTION | C(SP)-H | Iodine - chemistry | Oxidants - chemistry | Catalysis | Stereoisomerism | Palladium - chemistry | Synthesis | Oxidants | Oxidizing agents | Tolerances | Palladium | Ethers | Methylene | Iodine
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6. Full Text Iodine‐Catalyzed Oxidative Coupling Reactions Utilizing CH and XH as Nucleophiles
by Liu, Dong and Lei, Aiwen
Chemistry – An Asian Journal, ISSN 1861-4728, 04/2015, Volume 10, Issue 4, pp. 806 - 823
In recent decades, iodine‐catalyzed oxidative coupling reactions utilizing CH and XH as nucleophiles have received considerable attention because they... 
oxidation | reaction mechanisms | iodine | cross‐coupling | nucleophiles | Oxidation | Cross-coupling | Nucleophiles | Reaction mechanisms | Iodine | cross-coupling | MOLECULAR-IODINE | ENANTIOSELECTIVE ALPHA-TOSYLOXYLATION | CARBONYL-COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | M-CHLOROPERBENZOIC ACID | HYPERVALENT IODINE | DIRECT AMINATION | BOND ADJACENT | HYDROGEN-PEROXIDE | METAL-FREE | METHYL KETONES | Iodine - chemistry | Molecular Structure | Catalysis | Hydrogen Bonding | Oxidation-Reduction
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7. Full Text Alternative Strategies with Iodine: Fast Access to Previously Inaccessible Iodine(III) Compounds
by Hokamp, Tobias and Mollari, Leonardo and Wilkins, Lewis C and Melen, Rebecca L and Wirth, Thomas
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2018, Volume 57, Issue 27, pp. 8306 - 8309
Non‐iodinated arenes can be easily and selectively converted into (diacetoxyiodo)arenes in a single step under mild conditions by using iodine triacetates as... 
hypervalent iodine | iodine | one-pot reactions | aromatic substitution | stereoselective synthesis | REAGENTS | ACID | CLEAN OXIDATION | BOND-FORMING REACTIONS | CHEMISTRY, MULTIDISCIPLINARY | SODIUM PERBORATE | ALKENES | KETONES | HYPERVALENT IODINE(III) | FACILE | DERIVATIVES | Chemical tests and reagents | Iodine compounds | Organic chemistry | Purification | Aromatic compounds | Reagents | Chemical synthesis | Iodine
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8. Full Text An Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation
by Shao, Xinxin and Wang, Xueqiang and Yang, Tao and Lu, Long and Shen, Qilong
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2013, Volume 52, Issue 12, pp. 3457 - 3460
Sulfur and friends: A new electrophilic hypervalent iodine reagent 1 has been developed for direct trifluoromethylthiolation. A variety of nucleophiles,... 
hypervalent iodine | electrophilic addition | trifluoromethylthiolation | fluorine | NUCLEOPHILIC TRIFLUOROMETHYLATION | CONVENIENT SYNTHESIS | OXIDATIVE TRIFLUOROMETHYLTHIOLATION | SULFIDES | CATALYZED SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | SALT SYSTEM | DISULFIDES | ELEMENTAL SULFUR | ARYL BORONIC ACIDS | FLUORINATED ETHERS | Fluorides | Aromatic compounds | Amides | Sulfur | Nucleophiles | Aldehydes | Alkynes | Iodine
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9. Full Text Hypervalent Iodine‐Catalyzed Oxidative Functionalizations Including Stereoselective Reactions
by Singh, Fateh V and Wirth, Thomas
Chemistry – An Asian Journal, ISSN 1861-4728, 04/2014, Volume 9, Issue 4, pp. 950 - 971
Hypervalent iodine chemistry is now a well‐established area of organic chemistry. Novel hypervalent iodine reagents have been introduced in many different... 
hypervalent iodine | oxidants | stereoselective reactions | catalytic oxidations | rearrangement | P-TOLUENESULFONIC ACID | DESS-MARTIN PERIODINANE | ORGANIC-SYNTHESIS | ENANTIOSELECTIVE ALPHA-TOSYLOXYLATION | ANODIC GEM-DIFLUORINATION | IN-SITU GENERATION | CHEMISTRY, MULTIDISCIPLINARY | M-CHLOROPERBENZOIC ACID | O-IODOXYBENZOIC ACID | ELECTROLYTIC PARTIAL FLUORINATION | METAL-FREE
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10. Full Text Iodine(III)‐Mediated/Catalyzed Cycloisomerization–Amination Sequence of N‐Propargyl Carboxamides
by Okamura, Yuki and Sato, Daisuke and Yoshimura, Akira and Zhdankin, Viktor V and Saito, Akio
Advanced Synthesis & Catalysis, ISSN 1615-4150, 09/2017, Volume 359, Issue 18, pp. 3243 - 3247
(Diacetoxyiodo)benzene or iodine(III) catalyst, in situ generated from iodobenzene precatalyst with Oxone, promotes the cycloisomerization–amination sequence... 
amides | oxazoles | iodine | amination | cycloisomerization | ELECTRON-RICH AMINES | METAL-FREE CONDITIONS | CHEMISTRY, ORGANIC | BOND FORMATION | FREE 2+2+1 ANNULATION | PALLADIUM-CATALYZED DIAMINATION | UNACTIVATED ALKENES | AMIDES MILD ACCESS | OXIDATIVE CYCLOISOMERIZATION | HYPERVALENT IODINE(III) REAGENTS | CHEMISTRY, APPLIED | PALLADIUM(II)-CATALYZED INTRAMOLECULAR DIAMINATION | Oxazoles | Amides | Nitrogen | Benzene | Isomerization | Imides | Functional groups | Iodine
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