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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 Acetogenin Analogs Comprising Pyrimidine Moieties Linked by Amine Bonds and Their Inhibitory Activity against Human Cancer Cell Lines

Chemical and Pharmaceutical Bulletin, 2022/11/01, Vol.70(11), pp.823-826

2022

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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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Hydrazines and Azides via the Metal-Catalyzed Hydrohydrazination and Hydroazidation of Olefins

Journal of the American Chemical Society, 2006-09, Vol.128 (35), p.11693-11712

2006

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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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Regioselective SmI2-Mediated Radical ipso-Substitution Cyclization for the Construction of Pyrrolophenanthridinone Skeletons: The Synthesis of Amaryllidaceae Alkaloids

Chemical and Pharmaceutical Bulletin, 2023/07/01, Vol.71(7), pp.515-519

2023

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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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Cobalt-Catalyzed Hydroazidation of Olefins: Convenient Access to Alkyl Azides

Journal of the American Chemical Society, 2005-06, Vol.127 (23), p.8294-8295

2005

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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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Asymmetric Synthesis of Neolignans (−)-epi-Conocarpan and (+)-Conocarpan via Rh(II)-Catalyzed C−H Insertion Process and Revision of the Absolute Configuration of (−)-epi-Conocarpan

Journal of organic chemistry, 2009-06, Vol.74 (11), p.4418-4421

2009

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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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Diastereo- and Enantioselective Intramolecular 1,6-C–H Insertion Reaction of Diaryldiazomethanes Catalyzed by Chiral Dirhodium(II) Carboxylates

Heterocycles, 2021, Vol.103 (2), p.1078

2021

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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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A Polymer-Supported Chiral Fluorinated Dirhodium(II) Complex for Asymmetric Amination of Silyl Enol Ethers

Advanced synthesis & catalysis, 2012-08, Vol.354 (11-12), p.2331-2338

2012

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Asymmetric formal synthesis of (−)-pancracine via catalytic enantioselective C–H amination process

Tetrahedron, 2009-04, Vol.65 (16), p.3069-3077

2009

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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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Asymmetric approach to the pentacyclic skeleton of Aspidosperma alkaloids via enantioselective intramolecular 1,3-dipolar cycloaddition of carbonyl ylides catalyzed by chiral dirhodium(II) carboxylates

Tetrahedron letters, 2009-07, Vol.50 (26), p.3675-3678

2009

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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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Catalytic Asymmetric Synthesis of the endo-6-Aryl-8-oxabicyclo[3.2.1]oct-3-en-2-one Natural Product from Ligusticum chuanxing via 1,3-Dipolar Cycloaddition of a Formyl-Derived Carbonyl Ylide Using Rh2(S-TCPTTL)4

Journal of organic chemistry, 2010-09, Vol.75 (17), p.6039-6042

2010

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Stereoselective Total Synthesis of Myriocin Using Rhodium(II)-Catalyzed C−H Amination Followed by Alkylation

Asian journal of organic chemistry, 2015-11, Vol.4 (11), p.1246-1249

2015

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Catalytic asymmetric synthesis of descurainin via 1,3-dipolar cycloaddition of a carbonyl ylide using Rh2(R-TCPTTL)4

Tetrahedron letters, 2010-12, Vol.51 (50), p.6572-6575

2010

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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 Acetogenin Analogs Comprising Pyrimidine Moieties Linked by Amine Bonds and Their Inhibitory Activity against Human Cancer Cell Lines

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

Hydrazines and Azides via the Metal-Catalyzed Hydrohydrazination and Hydroazidation of Olefins

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

Regioselective SmI2-Mediated Radical ipso-Substitution Cyclization for the Construction of Pyrrolophenanthridinone Skeletons: The Synthesis of Amaryllidaceae Alkaloids

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

Cobalt-Catalyzed Hydroazidation of Olefins: Convenient Access to Alkyl Azides

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

Asymmetric Synthesis of Neolignans (−)-epi-Conocarpan and (+)-Conocarpan via Rh(II)-Catalyzed C−H Insertion Process and Revision of the Absolute Configuration of (−)-epi-Conocarpan

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

Diastereo- and Enantioselective Intramolecular 1,6-C–H Insertion Reaction of Diaryldiazomethanes Catalyzed by Chiral Dirhodium(II) Carboxylates

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

A Polymer-Supported Chiral Fluorinated Dirhodium(II) Complex for Asymmetric Amination of Silyl Enol Ethers

Asymmetric formal synthesis of (−)-pancracine via catalytic enantioselective C–H amination process

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

Asymmetric approach to the pentacyclic skeleton of Aspidosperma alkaloids via enantioselective intramolecular 1,3-dipolar cycloaddition of carbonyl ylides catalyzed by chiral dirhodium(II) carboxylates

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

Catalytic Asymmetric Synthesis of the endo-6-Aryl-8-oxabicyclo[3.2.1]oct-3-en-2-one Natural Product from Ligusticum chuanxing via 1,3-Dipolar Cycloaddition of a Formyl-Derived Carbonyl Ylide Using Rh2(S-TCPTTL)4

Stereoselective Total Synthesis of Myriocin Using Rhodium(II)-Catalyzed C−H Amination Followed by Alkylation

Catalytic asymmetric synthesis of descurainin via 1,3-dipolar cycloaddition of a carbonyl ylide using Rh2(R-TCPTTL)4

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