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Jun-ichi Sakaki

Tohoku University

37

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Derivatives of α,α,α′,α′‐Tetraaryl‐2,2‐ dimethyl‐1,3‐dioxolane‐4,5‐dimethanol (TADDOL) Containing Nitrogen, Sulfur and Phosphorus Atoms. New Ligands and Auxiliaries for Enantioselective Reactions.

2010 ChemInform
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Derivatives of α,α,α',α'-tetraaryl-2,2-dimethyl-1,3-dioxolan-4,5-dimethanol (TADDOL) containing nitrogen, sulfur, and phosphorus atoms. New ligands and auxiliaries for enantioselective reactions

1993 Tetrahedron
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1,3-Dioxin-4-ones and Related Compounds in Synthesis. Part 39. Enantioselective Synthesis of 1,3-Dioxin-4-ones Having 2,3-Dihydroxy- or 2,3,4-Trihydroxyalkyl Groups at the 6-Position: Versatile Building Blocks of Polyhydroxylated 4-7 Carbon Backbones.

1993 ChemInform
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Highly Enantioselective Reduction of Acetoacetylated Meldrum's Acid with Fermenting Bakers' Yeast.

1992 ChemInform
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Enantioselective Synthesis of (S)- and (R)-6-(2,3-Dihydroxypropyl)-1,3- dioxin-4-ones: Versatile Building Blocks of Four- and Six-Carbon Backbones.

1991 ChemInform
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Synthesis of Nucleosides and Their Related Compounds. Part 18. 1,3- Dipolar Cycloaddition of Di-(1-menthyl) Benzylidenemalonate to Z-N,. alpha.-Diphenylnitrone: Explanation for Diastereoselectivity.

1991 ChemInform
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Synthesis of 1,3‐Dioxin‐4‐ones and Their Use in Synthesis. Part 31. Two Lactone Formation Reactions from 1,3‐Dioxin‐4‐ones Having Hydroxyalkyl Group at the 6‐Position: Difference in Ring Opening and Closure.

1991 ChemInform
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Synthesis of 1,3-dioxin-4-ones having chiral hydroxyalkyl groups at the 6-position by means of baker's yeast reduction and their uses for epc synthesis

1991 Tetrahedron
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A Novel Synthesis of β-Keto Thioesters.

1991 ChemInform
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Enantioselective synthesis of (S)- and (R)-6-(2,3-dihydroxypropyl)-1,3-dioxin-4-ones: the versatile building blocks of four- and six-carbon backbones

1991 Journal of The Chemical Society, Chemical Communications
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Citations (6)