M. Matsugi

发表

Synthesis, reaction, and recycle of light fluorous Grubbs-Hoveyda catalysts for alkene metathesis.

D. Curran, M. Matsugi, 2005, The Journal of organic chemistry.

A fluorous Mukaiyama coupling reagent for a concise condensation reaction: utility of medium-fluorous strategy

Shuichi Nakamura, H. Hamamoto, T. Shioiri, 2012 .

Pronounced rate enhancements in condensation reactions attributed to the fluorous tag in modified Mukaiyama reagents

Shuichi Nakamura, T. Shioiri, Y. Sugiyama, 2010 .

Pummerer rearrangement using bis(p-nitrophenyl) phosphorazidate as an azidation reagent: A novel synthesis of azidomethyl sulfides

T. Shioiri, M. Matsugi, Kotaro Ishihara, 2017 .

Enhancement of stereoselectivities in asymmetric synthesis using fluorinated solvents, auxiliaries, and catalysts

H. Amii, H. Hamamoto, Tsuyuka Sugiishi, 2015 .

Asymmetric Henry Reaction Using a Double Fluorous-Tagged Co–Salen Complex

T. Shioiri, M. Matsugi, Asahi Fujino, 2022, SSRN Electronic Journal.

Practical synthesis of tetrazoles from amides and phosphorazidates in the presence of aromatic bases

T. Shioiri, M. Matsugi, Kotaro Ishihara, 2022, Tetrahedron.

An Expeditious Approach to Tetrazoles from Amides Utilizing Phosphorazidates.

T. Shioiri, M. Matsugi, Kotaro Ishihara, 2020, Organic letters.

Stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via a Beckmann rearrangement facilitated by diphenyl phosphorazidate

T. Shioiri, M. Matsugi, Kotaro Ishihara, 2019, Tetrahedron Letters.

The systematic structure-activity relationship to predict how flavones bind to human androgen receptor for their antagonistic activity.

M. Akamatsu, A. Hosoda, H. Tamura, 2013, Bioorganic & medicinal chemistry.

A recyclable and highly stereoselective multi-fluorous proline catalyst for asymmetric aldol reactions

Machiko Gotoh, T. Shioiri, M. Matsugi, 2020 .

A medium fluorous Grubbs–Hoveyda 2nd generation catalyst for phase transfer catalysis of ring closing metathesis reactions

Tomoko Watanabe, H. Hamamoto, T. Shioiri, 2015 .

Efficient synthesis of thioesters and amides from aldehydes by using an intermolecular radical reaction in water.

Y. Kita, H. Nambu, M. Matsugi, 2005, Chemistry.

Development of efficient processes for multi-gram scale and divergent preparation of fluorous-Fmoc reagents

H. Hamamoto, T. Shioiri, Y. Sugiyama, 2015 .

SNAr azidation of phenolic functions utilizing diphenyl phosphorazidate

T. Shioiri, M. Matsugi, Kotaro Ishihara, 2020 .

Efficient stereoselective synthesis of α-C-glycopyranosides using 2,2′-azobis(2,4-dimethyl-4-methoxyvaleronitrile) [V-70]

Y. Kita, M. Matsugi, M. Oka, 1999 .

1H NMR determination of absolute configuration of 1- or 2-aryl-substituted alcohols and amines by means of their diastereomers: novel separation technique of diastereomeric derivatives of pyridyl alcohols by extraction.

Y. Kita, M. Nojima, M. Matsugi, 2002, Chemistry.

An alternative and facile purification procedure of amidation and esterification reactions using a medium fluorous Mukaiyama reagent

M. Matsugi, Yoko Kunda, S. Oka, 2008 .

Preparation and condensation reactions of a new light-fluorous Mukaiyama reagent: reliable purification with fluorous solid phase extraction for esters and amides

Y. Mori, A. Masuyama, Sachi Okamoto, 2007 .

Unprecedented Asymmetric Epoxidation of Isolated Carbon-Carbon Double Bonds by a Chiral Fluorous Fe(III) Salen Complex: Exploiting Fluorophilic Effect for Catalyst Design

Yuta Suzuki, Y. Yoshida, T. Shioiri, 2019, European Journal of Organic Chemistry.

Radical Addition Reaction of Brominated Active Methylene Compounds to Enol Ethers Using 2,2‘-Azobis(2,4- dimethyl-4-methoxyvaleronitrile) (V-70) as an Initiator

Y. Kita, T. Yamaguchi, M. Matsugi, 1999 .

Practical Radical Additions under Mild Conditions Using 2,2‘-Azobis(2,4-dimethyl-4-methoxyvaleronitrile) [V-70] as an Initiator

Y. Kita, T. Yamaguchi, M. Matsugi, 1998 .

Additions of malononitrile radicals to alkenes under mild conditions using 2,2′-azobis-(2,4-dimethyl-4-methoxyvaleronitrile) (V-70) as an initiator

Y. Kita, T. Yamaguchi, M. Matsugi, 1997 .

A novel and efficient methodology for the C-C bond forming radical cyclization of hydrophobic substrates in water.

Y. Kita, H. Nambu, G. Anilkumar, 2001, Organic letters.

A Practical Synthesis of 5-Substituted 1H-Tetrazoles from Aldoximes Employing the Azide Anion from Diphenyl Phosphorazidate

Takatoshi Matsumoto, T. Shioiri, M. Matsugi, 2017 .

A highly stereoselective synthesis of α-linked C-glycopyranosides using 2,2′-azobis-(2,4-dimethyl-4-methoxyvaleronitrile) (V-70)

Y. Kita, M. Matsugi, M. Oka, 1997 .

An efficient methodology for the C–C bond forming radical cyclization of hydrophobic substrates in water: effect of additive on radical reaction in water

Y. Kita, H. Nambu, G. Anilkumar, 2003 .

Doebner—Miller Synthesis in a Two-Phase System: Practical Preparation of Quinolines.

F. Tabusa, M. Matsugi, J. Minamikawa, 2001 .

Doebner–Miller synthesis in a two-phase system: practical preparation of quinolines

F. Tabusa, M. Matsugi, J. Minamikawa, 2000 .

Synthesis of 5-Substituted 1H-Tetrazoles from Aldoximes Using Diphenyl Phosphorazidate

T. Shioiri, M. Matsugi, Kotaro Ishihara, 2016 .

Asymmetric pummerer rearrangement and related reactions

Y. Kita, N. Shibata, M. Matsugi, 2000 .

Synthesis of carbamoyl azides via the Lossen rearrangement utilizing diphenyl phosphorazidate

T. Shioiri, M. Matsugi, Kotaro Ishihara, 2022, Tetrahedron Letters.

Catalytic asymmetric oxidation of sulfide with titanium–mandelic acid complex: practical synthesis of (S)-3-[1-(2-methylphenyl)imidazol-2-ylsulfinyl]propan-1-ol, the key intermediate of OPC-29030

N. Fukuda, M. Matsugi, S. Otsuka, 2001 .

Practical asymmetric oxidation of 3-[1-(2-methylphenyl) imidazol-2-ylthio]propan-1-ol based on a titanium-mandelic acid complex

N. Fukuda, M. Matsugi, S. Otsuka, 1998 .

Asymmetric synthesis of a xanthine dehydrogenase inhibitor (S)-(−)-BOF-4272: Utility of chiral alkoxysulfonium salts

T. Furuta, N. Fukuda, K. Hashimoto, 1995 .

Highly asymmetric Pummerer-type reaction induced by ethoxy vinyl esters

Y. Kita, N. Shibata, M. Matsugi, 1997 .

ASYMMETRIC SYNTHESIS OF A XANTHINE DEHYDROGENASE INHIBITOR (S)-(-)-BOF-4272 : MECHANISM OF CHIRAL DIARYL SULFOXIDE FORMATION

Y. Kurogi, N. Fukuda, K. Hashimoto, 1997 .

Lipase-catalyzed domino kinetic resolution/intramolecular Diels-Alder reaction: one-pot synthesis of optically active 7-oxabicyclo[2.2.1]heptenes from furfuryl alcohols and beta-substituted acrylic acids.

Y. Kita, S. Akai, M. Imanishi, 2002, Chemistry.

Concise Synthesis of Peptide Analogs Using a Fluorous-Fmoc Protection Strategy

M. Matsugi, 2017 .

A synthesis of all stereoisomers of tenuecyclamide A employing a fluorous-Fmoc strategy.

K. Hayashi, Hiroaki Takahashi, H. Hamamoto, 2013, The Journal of organic chemistry.

Fluorous mixture synthesis of fluorous-Fmoc reagents using a one-pot double tagging strategy

H. Hamamoto, Y. Sugiyama, Y. Masuda, 2013 .

Synthesis of fluorous-FMOC reagents and purification of protected dipeptides with fluorous solid phase extraction

D. Curran, M. Matsugi, M. Hasegawa, 2006 .

A solvent-free synthesis of 4-aryl-NH-1,2,3-triazoles from ketones utilizing diphenyl phosphorazidate

T. Shioiri, Shota Shibuya, M. Matsugi, 2022, Synthetic Communications.

Additions of Malononitrile Radicals to Alkenes under Mild Conditions Using 2,2′‐Azobis‐(2,4‐dimethyl‐4‐methoxyvaleronitrile) (V‐70) as an Initiator.

Y. Kita, T. Yamaguchi, M. Matsugi, 1997 .

A comparative study of the asymmetric epoxidation of aromatic olefins using the first generation manganese salen epoxidation catalysts and their light fluorous variants: an interesting discovery on the use of benzotrifluoride as a cosolvent

H. Hamamoto, T. Shioiri, Y. Sugiyama, 2014 .

Reverse fluorous solid-phase extraction: a new technique for rapid separation of fluorous compounds.

D. Curran, M. Matsugi, 2004, Organic letters.

The direct synthesis of thioesters using an intermolecular radical reaction of aldehydes with dipentafluorophenyl disulfide in water.

Y. Kita, H. Nambu, M. Matsugi, 2002, Chemical communications.

A simple determination method of the absolute configuration of 1-arylethanthiols by an intramolecular CH/pi shielding effect in 1H-NMR of diastereomeric thiol esters.

Y. Kita, M. Nojima, M. Matsugi, 2003, Chemical & pharmaceutical bulletin.

[4 cases of pathologic rupture of the extensor communis tendons due to non-specific tenosynovitis caused by farm work].

M. Matsugi, T. Mitsui, H. Tanaka, 1967, Seikeigeka. Orthopedic surgery.

Direct perfluoroalkylation of non-activated aromatic C–H bonds of phenols

Toshiya Hayashi, M. Matsugi, S. Haga, 2008 .

N-Methylated tetrapeptide synthesis via sequential filtration procedures based on TeflonTM immobilization utilizing the properties of fluorous 9-fluorenylmethyl ester

T. Shioiri, M. Matsugi, Kotaro Ishihara, 2023, Tetrahedron Letters.

Effective nonenzymatic kinetic resolution of (′)-trans-2-arylcyclohexanols using 3β-acetoxyetienic acid, DCC, and DMAP

Y. Kita, M. Nojima, M. Matsugi, 2003 .

An effective synthesis of 5,4'-disubstituted flavones via a cesium enolate assisted intramolecular ipso-substitution reaction.

H. Tamura, T. Shioiri, M. Takeda, 2010, Chemical & pharmaceutical bulletin.

Synthesis and RCM reactions using a recyclable Grubbs-Hoveyda metathesis catalyst activated by a light fluorous tag.

T. Shioiri, M. Matsugi, Yuki Tsuchiya, 2010, The Journal of organic chemistry.

Fluorous Columns are Superior to Cyclodextrin Columns for Demixing in Fluorous Mixture Synthesis: When and Why to Use Fluorous Silica Gel

D. Curran, Sivaraman Dandapani, S. Werner, 2004 .

Determination of absolute configuration of trans-2-arylcyclohexanols using remarkable aryl-induced 1H NMR shifts in diastereomeric derivatives

Y. Kita, M. Nojima, M. Matsugi, 2001 .

A novel efficient sulfenylation method using quinonemono-O,S-acetals under mild conditions

Y. Kita, M. Matsugi, K. Murata, 1997 .

Facile and efficient sulfenylation method using quinone mono-O,S-acetals under mild conditions.

Y. Kita, H. Nambu, G. Anilkumar, 2001, The Journal of organic chemistry.

An efficient sulfenylation of aromatics using highly active quinone mono O,S-acetal bearing a pentafluorophenylthio group

Y. Kita, H. Nambu, M. Matsugi, 2001 .

A Nonenzymatic Kinetic Resolution of (±)-trans-2-Arylcyclohexanols via Esterification Using Polymer-Supported DCC, DMAP, and 3β-Acetoxyetienic Acid

M. Matsugi, Atsushi Miyazaki, Yukimoto Kobayashi, 2013 .