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Synthesis of biologically active pentapeptide analogs of the N-terminal part of lipoprotein from the outer membrane of Escherichia coli.
Newly synthesized lipopentapeptide derivatives with (R___-)-glycerol moieties showed higher mitogenic activities than those with the (S___-)-configuration.
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Synthesis of optically active lipopeptide analogs from the outer membrane of Escherichia coli.
The synthesis of optically active lipopeptide derivatives has been accomplished by the use of chiral glycerol derivatives. Lipopeptide derivatives with (R)-glycerol moieties showed higher mitogenicExpand
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Prostanoids and related compounds. VII. Synthesis and inhibitory activity of 1-isoindolinone derivatives possessing inhibitory activity against thromboxane A2 analog (U-46619)-induced
We have synthesized a series of novel 1-isoindolinone derivatives, which inhibited the contraction of pig coronary artery induced by U-46619, a thromboxane A2 analog.
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Synthesis of styrenes through the biocatalytic decarboxylation of trans-cinnamic acids by plant cell cultures.
A novel method for producing styrenes from trans-cinnamic acids was developed. When trans-cinnamic acid was incubated with plant cell cultures at room temperature, styrene was obtained.Expand
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Zinc-metal promoted selective α-haloacylation and gem-bisacylation of alkyl aldehydes in the presence of chlorotrimethylsilane
Treatment of a mixture of alkyl aldehydes (1) with acid chlorides (2) in the presence of zinc metal powder and a catalytic amount of chlorotrimethylsilane (TMSCl) in dichloromethane brought aboutExpand
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Effect of inhibitor or immobilization on reduction of benzoylpyridines by baker's yeast.
The stereochemical course of the reduction of benzoylpyridine derivatives (1a-e) by baker's yeast can be modified by immobilization or by treating the reduction system with allyl alcohol or ethylExpand
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Synthesis of the 2',3'-dideoxynucleoside derivatives of the specific binding peptide part of CD4.
The 2', 3'-dideoxynucleoside derivatives of the specific binding peptide part of CD4 to HIV envelope protein gp120 were synthesized.
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Synthesis of the 2',3'-dideoxynucleoside derivatives of the specific binding peptide part of CD4.
The 2',3'-dideoxynucleoside derivatives of the specific binding peptide part of CD4 to HIV envelope protein gp120 were synthesized.
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Synthesis of optically active alpha-phenylpyridylmethanols with baker's yeast.
We have synthesized optically active alpha-phenylpyridylmethanols by using free baker's yeast (FBY) in water, immobilized baker's yeast (IMBY) in water, and IMBY in hexane.