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Recent topics in application of selective Rh(II)-catalyzed C H functionalization toward natural product synthesis

Tetrahedron letters, 2018-01, Vol.59 (3), p.188-202

2018

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Ring-Opening Cyclization of Spirocyclopropanes Using Sulfoxonium Ylides

Chemical and Pharmaceutical Bulletin, 2020/05/01, Vol.68(5), pp.479-486

2020

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Synthesis of Sphingosine-Related Azetidine Alkaloids, Penaresidins: Construction of Highly Substituted Azetidine Rings

Heterocycles, 2020, Vol.101 (2), p.383

2020

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Iodide‐Catalyzed Ring‐Opening Cyclization of Cyclohexane‐1,3‐dione‐2‐spirocyclopropanes

Advanced synthesis & catalysis, 2018-08, Vol.360 (15), p.2938-2944

2018

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Total Synthesis of Sphingofungin E and 4,5-Di-epi-sphingofungin E

Chemical and Pharmaceutical Bulletin, 2017/07/01, Vol.65(7), pp.687-696

2017

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8-Iodoisoquinolinone, a Conformationally Rigid Highly Reactive 2-Iodobenzamide Catalyst for the Oxidation of Alcohols by Hypervalent Iodine

Chemical and Pharmaceutical Bulletin, 2024/02/27, Vol.72(2), pp.234-239

2024

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Efficient and Environmentally Benign Oxidative Cleavage of Pyrrolidine-2-methanols to γ-Lactams Using 2-Iodobenzamide as a Catalyst and Oxone

Chemical and Pharmaceutical Bulletin, 2024/01/17, Vol.72(1), pp.75-79

2024

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An efficient synthesis of cycloalkane-1,3-dione-2-spirocyclopropanes from 1,3-cycloalkanediones using (1-aryl-2-bromoethyl)-dimethylsulfonium bromides: application to a one-pot synthesis of tetrahydroindol-4(5H)-one

Tetrahedron letters, 2015-07, Vol.56 (29), p.4312-4315

2015

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Acid-Catalyzed Ring-Opening Cyclization of Spirocyclopropanes for the Construction of a 2-Arylbenzofuran Skeleton: Total Synthesis of Cuspidan B

Synthesis (Stuttgart), 2016-06, Vol.48 (12), p.1892-1901

2016

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2-Iodo- N -isopropyl-5-methoxybenzamide as a highly reactive and environmentally benign catalyst for alcohol oxidation

Beilstein journal of organic chemistry, 2018-04, Vol.14 (1), p.971-978

2018

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Useful procedures for fluorocyclization of tryptamine and tryptophol derivatives to 3a-fluoropyrrolo[2,3-b]indoles and 3a-fluorofuro[2,3-b]indoles

Journal of fluorine chemistry, 2014-09, Vol.165, p.7-13

2014

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Synthesis and biological evaluation of 2-epi-jaspine B analogs as selective sphingosine kinase 1 inhibitors

Bioorganic chemistry, 2020-05, Vol.98, p.103369, Article 103369

2020

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Total Synthesis of (+)-Tanikolide by a Traceless Stereoinduction Method Using Rhodium(II)-Catalyzed Oxonium Ylide Formation–[2,3]-Sigmatropic Rearrangement and NHC-Catalyzed Ring-Expansion Lactonization

Synlett, 2016-01, Vol.27 (7), p.1106-1009

2016

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Novel 2,2,6,6-Tetramethylpiperidine 1-Oxyl-Iodobenzene Hybrid Catalyst for Oxidation of Primary Alcohols to Carboxylic Acids

Advanced synthesis & catalysis, 2011-04, Vol.353 (6), p.855-859

2011

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An Efficient Method for the Synthesis of 2′,3′-Nonsubstituted Cycloalkane-1,3-dione-2-spirocyclopropanes Using (2-Bromoethyl)diphenylsulfonium Trifluoromethanesulfonate

Chemical and Pharmaceutical Bulletin, 2016/12/01, Vol.64(12), pp.1763-1768

2016

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Total synthesis of myriocin and mycestericin D employing Rh(II)-catalyzed C H amination followed by stereoselective alkylation

Tetrahedron, 2017-02, Vol.73 (7), p.868-878

2017

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Stereoselective Alkylation of Oxathiazinane N,O-Ketals for the Construction of Aza-Quaternary Carbon Centers

Heterocycles, 2021, Vol.103 (1), p.425

2021

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A Novel Catalytic Hypervalent Iodine Oxidation of p-Alkoxyphenols to p-Quinones Using 4-Iodophenoxyacetic Acid and Oxone

Synlett, 2007-03, Vol.2007 (5), p.0765-0768

2007

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An Efficient Catalytic Oxidation of p-Alkoxypenols to p-Quinones Using Tetrabutylammonium Bromide and Oxone

Chemical and Pharmaceutical Bulletin, 2011/01/01, Vol.59(1), pp.132-134

2011

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Efficient Synthesis of p-Quinols Using Catalytic Hypervalent Iodine Oxidation of 4-Arylphenols with 4-Iodophenoxyacetic Acid and Oxone

Chemical and Pharmaceutical Bulletin, 2009/06/01, Vol.57(6), pp.643-645

2009

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Enantioselective Synthesis of Pachastrissamine (Jaspin B) Using Dirhodium(II)-Catalyzed C–H Amination and Asymmetric Dihydroxylation as Key Steps

Chemical and Pharmaceutical Bulletin, 2007/08/01, Vol.55(8), pp.1284-1286

2007

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Practical Synthesis of Pachastrissamine (Jaspine B), 2-epi-Pachastrissamine, and the 2-epi-Pyrrolidine Analogue

Chemical and Pharmaceutical Bulletin, 2016/02/01, Vol.64(2), pp.179-188

2016

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Recyclable Magnetic Nanoparticle-Supported Iodoarene Catalysts for Oxidation of 4-Alkoxyphenols to Quinones

Asian journal of organic chemistry, 2016-04, Vol.5 (4), p.486-489

2016

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Synthetic Studies on a Pachastrissamine Sulfur Analogue: Synthesis of a 4-epi-Sulfur Analogue

Chemical and Pharmaceutical Bulletin, 2016/04/01, Vol.64(4), pp.366-370

2016

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Synthetic Studies on a Pachastrissamine Sulfur Analogue : Synthesis of a 4-epi-Sulfur Analogue

Chemical and Pharmaceutical Bulletin, 2016-04, Vol.64 (4), p.366-370

2016

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Recent topics in application of selective Rh(II)-catalyzed C H functionalization toward natural product synthesis

Ring-Opening Cyclization of Spirocyclopropanes Using Sulfoxonium Ylides

Synthesis of Sphingosine-Related Azetidine Alkaloids, Penaresidins: Construction of Highly Substituted Azetidine Rings

Iodide‐Catalyzed Ring‐Opening Cyclization of Cyclohexane‐1,3‐dione‐2‐spirocyclopropanes

Total Synthesis of Sphingofungin E and 4,5-Di-epi-sphingofungin E

8-Iodoisoquinolinone, a Conformationally Rigid Highly Reactive 2-Iodobenzamide Catalyst for the Oxidation of Alcohols by Hypervalent Iodine

Efficient and Environmentally Benign Oxidative Cleavage of Pyrrolidine-2-methanols to γ-Lactams Using 2-Iodobenzamide as a Catalyst and Oxone

An efficient synthesis of cycloalkane-1,3-dione-2-spirocyclopropanes from 1,3-cycloalkanediones using (1-aryl-2-bromoethyl)-dimethylsulfonium bromides: application to a one-pot synthesis of tetrahydroindol-4(5H)-one

Acid-Catalyzed Ring-Opening Cyclization of Spirocyclopropanes for the Construction of a 2-Arylbenzofuran Skeleton: Total Synthesis of Cuspidan B

2-Iodo- N -isopropyl-5-methoxybenzamide as a highly reactive and environmentally benign catalyst for alcohol oxidation

Useful procedures for fluorocyclization of tryptamine and tryptophol derivatives to 3a-fluoropyrrolo[2,3-b]indoles and 3a-fluorofuro[2,3-b]indoles

Synthesis and biological evaluation of 2-epi-jaspine B analogs as selective sphingosine kinase 1 inhibitors

Total Synthesis of (+)-Tanikolide by a Traceless Stereoinduction Method Using Rhodium(II)-Catalyzed Oxonium Ylide Formation–[2,3]-Sigmatropic Rearrangement and NHC-Catalyzed Ring-Expansion Lactonization

Novel 2,2,6,6-Tetramethylpiperidine 1-Oxyl-Iodobenzene Hybrid Catalyst for Oxidation of Primary Alcohols to Carboxylic Acids

An Efficient Method for the Synthesis of 2′,3′-Nonsubstituted Cycloalkane-1,3-dione-2-spirocyclopropanes Using (2-Bromoethyl)diphenylsulfonium Trifluoromethanesulfonate

Total synthesis of myriocin and mycestericin D employing Rh(II)-catalyzed C H amination followed by stereoselective alkylation

Stereoselective Alkylation of Oxathiazinane N,O-Ketals for the Construction of Aza-Quaternary Carbon Centers

A Novel Catalytic Hypervalent Iodine Oxidation of p-Alkoxyphenols to p-Quinones Using 4-Iodophenoxyacetic Acid and Oxone

An Efficient Catalytic Oxidation of p-Alkoxypenols to p-Quinones Using Tetrabutylammonium Bromide and Oxone

Efficient Synthesis of p-Quinols Using Catalytic Hypervalent Iodine Oxidation of 4-Arylphenols with 4-Iodophenoxyacetic Acid and Oxone

Enantioselective Synthesis of Pachastrissamine (Jaspin B) Using Dirhodium(II)-Catalyzed C–H Amination and Asymmetric Dihydroxylation as Key Steps

Practical Synthesis of Pachastrissamine (Jaspine B), 2-epi-Pachastrissamine, and the 2-epi-Pyrrolidine Analogue

Recyclable Magnetic Nanoparticle-Supported Iodoarene Catalysts for Oxidation of 4-Alkoxyphenols to Quinones

Synthetic Studies on a Pachastrissamine Sulfur Analogue: Synthesis of a 4-epi-Sulfur Analogue

Synthetic Studies on a Pachastrissamine Sulfur Analogue : Synthesis of a 4-epi-Sulfur Analogue

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