Toshiro Ibuka scite author profile

Palladium(0)-catalyzed reactions of N-methanesulfonyl- or N-(arenesulfonyl)-3-alkyl-2-vinylaziridines reveal that 2,3-cis-isomers are more stable than the corresponding 2,3-trans-isomers in accord with ab initio calculations. A highly stereoselective synthetic route to (E)-alkene dipeptide isosteres having desired stereochemistries from 2,3-cis-3-isobutyl-2-vinylaziridine by the use of organocopper chemistry is also presented.

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Z-Selective Horner−Wadsworth−Emmons Reaction of Ethyl (Diarylphosphono)acetates Using Sodium Iodide and DBU

Ando

Oishi²,

Hirama³

et al. 2000

J. Org. Chem.

155

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The aza-Payne rearrangement: a synthetically valuable equilibration

Ibuka¹

1998

Chem. Soc. Rev.

135

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A novel anti-HIV synthetic peptide, T-22 ([Tyr5,12,Lys7]-polyphemusin II)

Masuda

Nakashima

Ueda

et al. 1992

Biochemical and Biophysical Research Communications

120

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Pharmacophore identification of a chemokine receptor (CXCR4) antagonist, T22 ([Tyr 5,12 , Lys 7 ]-polyphemusin II), which specifically blocks T cell-line-tropic HIV-1 infection

Tamamura

Imai

Ishihara

et al. 1998

Bioorganic & Medicinal Chemistry

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Effective lowly cytotoxic analogs of an HIV-cell fusion inhibitor, T22 ([Tyr5,12, Lys7]-polyphemusin II)

Tamamura¹,

Arakaki²,

Funakoshi³

et al. 1998

Bioorganic & Medicinal Chemistry

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Toshiro Ibuka

A Low-Molecular-Weight Inhibitor against the Chemokine Receptor CXCR4: A Strong Anti-HIV Peptide T140

Synthesis of Protegrin-Related Peptides and Their Antibacterial and Anti-human Immunodeficiency Virus Activity.

A Thermodynamic Preference of Chiral N-Methanesulfonyl and N-Arenesulfonyl 2,3-cis-3-Alkyl-2-Vinylaziridines over Their 2,3-Trans-Isomers: Useful Palladium(0)-Catalyzed Equilibration Reactions for the Synthesis of (E)-Alkene Dipeptide Isosteres

Z-Selective Horner−Wadsworth−Emmons Reaction of Ethyl (Diarylphosphono)acetates Using Sodium Iodide and DBU

The aza-Payne rearrangement: a synthetically valuable equilibration

A novel anti-HIV synthetic peptide, T-22 ([Tyr5,12,Lys7]-polyphemusin II)

Pharmacophore identification of a chemokine receptor (CXCR4) antagonist, T22 ([Tyr 5,12 , Lys 7 ]-polyphemusin II), which specifically blocks T cell-line-tropic HIV-1 infection

Effective lowly cytotoxic analogs of an HIV-cell fusion inhibitor, T22 ([Tyr5,12, Lys7]-polyphemusin II)

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