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First enantioselective synthesis of (-)- and (+)-virgatusin, tetra-substituted tetrahydrofuran lignan

Organic & biomolecular chemistry, 2005-05, Vol.3 (9), p.1670-1675

2005

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Regulated-Stereoselective Construction of Thirteen Stereogenic Centers Necessary for the Frame of (+)-Discodermolide, Based on Iterative Lewis Acid-Promoted Aldol Reactions

Journal of organic chemistry, 2003-10, Vol.68 (21), p.7967-7978

2003

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Stereoselective Synthesis of the Neolignan, (+)-Dehydrodiconiferyl Alcohol

Bioscience, biotechnology, and biochemistry, 2001-05, Vol.65 (5), p.1134-1140

2001

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Systematic Strategy for the Synthesis of Cyanobacterin and Its Stereoisomers. 1. Asymmetric Total Synthesis of Dechloro-cyanobacterin and Its Enantiomer

Bioscience, biotechnology, and biochemistry, 2003, Vol.67 (10), p.2183-2193

2003

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Systematic Strategy for the Synthesis of Cyanobacterin and Its Stereoisomers. 2. Asymmetric Total Synthesis of the 2- and 3-Epimers of Dechloro-cyanobacterin

Bioscience, biotechnology, and biochemistry, 2003, Vol.67 (10), p.2215-2223

2003

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Improved Procedure for the Enantiometric Synthesis of 1-Hydroxy/acetoxy-2,6-diaryl-3,7-dioxabicyclo[3.3.0] octane Lignans: Total Syntheses of (+)-Paulownin, (+)-Phrymarin I and (+)-Phrymarin II

Bioscience, biotechnology, and biochemistry, 2001-01, Vol.65 (1), p.29-34

2001

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Superior substrate control on diastereoselection in boric Lewis acid-promoted aldol reactions. Asymmetric synthesis of a 3,4- syn homologous series of ethyl 3,5-dihydroxy-2,4-dimethyl-5-phenylpentanoates

Tetrahedron: asymmetry, 2001-09, Vol.12 (16), p.2343-2349

2001

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Effect of optically active ethyl 2-phthalimidooxypropionate on the growth of cress, Lepidium sativum

Bioscience, biotechnology, and biochemistry, 1999, Vol.63 (10), p.1831-1833

1999

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Total Synthesis of (+)-Paulownin

Bioscience, biotechnology, and biochemistry, 1997, Vol.61 (4), p.743-745

1997

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Total Synthesis of (+)-Phrymarolin I from (+)-Malic Acid

Bioscience, biotechnology, and biochemistry, 1997, Vol.61 (4), p.660-663

1997

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Systematic Strategy for the Synthesis of Cyanobacterin and Its Stereoisomers. 2. Asymmetric Total Synthesis of the 2- and 3-Epimers of Dechloro-cyanobacterin

Bioscience, biotechnology, and biochemistry, 2003-10, Vol.67 (10), p.2183-2193

2003

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Systematic Strategy for the Synthesis of Cyanobacterin and Its Stereoisomers. 1. Asymmetric Total Synthesis of Dechloro-cyanobacterin and Its Enantiomer

Bioscience, biotechnology, and biochemistry, 2003-10, Vol.67 (10), p.2215-2223

2003

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A straightforward, highly stereoselective construction of eight stereogenic centers in (+)-discodermolide C1–C13 segment, based on a strategy of iterative aldol reactions

Tetrahedron letters, 2002-09, Vol.43 (36), p.6377-6381

2002

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A straightforward, highly stereoselective construction of eight stereogenic centers in (+)-discodermolide C 1–C 13 segment, based on a strategy of iterative aldol reactions

Tetrahedron letters, 2002-09, Vol.43 (36), p.6377-6381

2002

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A short synthesis of the C15–C21 segment of (+)-discodermolide, based on an asymmetric approach from achiral 2-methyl-1,3-propanediol to versatile enantiopure stereotriads

Tetrahedron letters, 2002-09, Vol.43 (36), p.6373-6376

2002

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A short synthesis of the C 15–C 21 segment of (+)-discodermolide, based on an asymmetric approach from achiral 2-methyl-1,3-propanediol to versatile enantiopure stereotriads

Tetrahedron letters, 2002-09, Vol.43 (36), p.6373-6376

2002

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Corrigendum to “A straightforward, highly stereoselective construction of eight stereogenic centers in (+)-discodermolide C1–C13 segment, based on a strategy of iterative aldol reactions”

Tetrahedron letters, 2003-02, Vol.44 (7), p.1519-1520

2003

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Corrigendum to “A straightforward, highly stereoselective construction of eight stereogenic centers in (+)-discodermolide C 1–C 13 segment, based on a strategy of iterative aldol reactions” : [Tetrahedron Lett. 43 (2002) 6377]

Tetrahedron letters, 2003, Vol.44 (7), p.1519-1520

2003

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Improved Procedure for the Enantiometric Synthesis of 1-Hydroxy/acetoxy-2,6-diaryl-3,7-dioxabicyclo[3.3.0] octane Lignans

Bioscience, biotechnology, and biochemistry, 2001-01, Vol.65 (1), p.29

2001

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Versatile, high 2,4-syn dialkyl diastereoselection in the radical debromination of α-bromo-α-methyl-δ-valerolactones with tri-n-butyltin hydride and a catalytic amount of triethylborane

Tetrahedron letters, 2001-10, Vol.42 (41), p.7299-7301

2001

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First Enantioselective Synthesis of (-)- and (+)-Virgatusin (I), a Tetrasubstituted Tetrahydrofuran Lignan

ChemInform, 2005-10, Vol.36 (40), p.no-no

2005

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ChemInform Abstract: Versatile, High 2,4-syn Dialkyl Diastereoselection in the Radical Debromination of α-Bromo-α-methyl-δ-valerolactones with Tri-n-butyltin Hydride and a Catalytic Amount of Triethylborane

ChemInform, 2002-01, Vol.33 (2), p.no-no

2002

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First enantioselective synthesis of (-)- and (+)-virgatusin, tetra-substituted tetrahydrofuran lignan

Regulated-Stereoselective Construction of Thirteen Stereogenic Centers Necessary for the Frame of (+)-Discodermolide, Based on Iterative Lewis Acid-Promoted Aldol Reactions

Stereoselective Synthesis of the Neolignan, (+)-Dehydrodiconiferyl Alcohol

Systematic Strategy for the Synthesis of Cyanobacterin and Its Stereoisomers. 1. Asymmetric Total Synthesis of Dechloro-cyanobacterin and Its Enantiomer

Systematic Strategy for the Synthesis of Cyanobacterin and Its Stereoisomers. 2. Asymmetric Total Synthesis of the 2- and 3-Epimers of Dechloro-cyanobacterin

Improved Procedure for the Enantiometric Synthesis of 1-Hydroxy/acetoxy-2,6-diaryl-3,7-dioxabicyclo[3.3.0] octane Lignans: Total Syntheses of (+)-Paulownin, (+)-Phrymarin I and (+)-Phrymarin II

Superior substrate control on diastereoselection in boric Lewis acid-promoted aldol reactions. Asymmetric synthesis of a 3,4- syn homologous series of ethyl 3,5-dihydroxy-2,4-dimethyl-5-phenylpentanoates

Effect of optically active ethyl 2-phthalimidooxypropionate on the growth of cress, Lepidium sativum

Total Synthesis of (+)-Paulownin

Total Synthesis of (+)-Phrymarolin I from (+)-Malic Acid

Systematic Strategy for the Synthesis of Cyanobacterin and Its Stereoisomers. 2. Asymmetric Total Synthesis of the 2- and 3-Epimers of Dechloro-cyanobacterin

Systematic Strategy for the Synthesis of Cyanobacterin and Its Stereoisomers. 1. Asymmetric Total Synthesis of Dechloro-cyanobacterin and Its Enantiomer

A straightforward, highly stereoselective construction of eight stereogenic centers in (+)-discodermolide C1–C13 segment, based on a strategy of iterative aldol reactions

A straightforward, highly stereoselective construction of eight stereogenic centers in (+)-discodermolide C 1–C 13 segment, based on a strategy of iterative aldol reactions

A short synthesis of the C15–C21 segment of (+)-discodermolide, based on an asymmetric approach from achiral 2-methyl-1,3-propanediol to versatile enantiopure stereotriads

A short synthesis of the C 15–C 21 segment of (+)-discodermolide, based on an asymmetric approach from achiral 2-methyl-1,3-propanediol to versatile enantiopure stereotriads

Corrigendum to “A straightforward, highly stereoselective construction of eight stereogenic centers in (+)-discodermolide C1–C13 segment, based on a strategy of iterative aldol reactions”

Corrigendum to “A straightforward, highly stereoselective construction of eight stereogenic centers in (+)-discodermolide C 1–C 13 segment, based on a strategy of iterative aldol reactions” : [Tetrahedron Lett. 43 (2002) 6377]

Improved Procedure for the Enantiometric Synthesis of 1-Hydroxy/acetoxy-2,6-diaryl-3,7-dioxabicyclo[3.3.0] octane Lignans

Versatile, high 2,4-syn dialkyl diastereoselection in the radical debromination of α-bromo-α-methyl-δ-valerolactones with tri-n-butyltin hydride and a catalytic amount of triethylborane

First Enantioselective Synthesis of (-)- and (+)-Virgatusin (I), a Tetrasubstituted Tetrahydrofuran Lignan

ChemInform Abstract: Versatile, High 2,4-syn Dialkyl Diastereoselection in the Radical Debromination of α-Bromo-α-methyl-δ-valerolactones with Tri-n-butyltin Hydride and a Catalytic Amount of Triethylborane

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