• Archives of Pharmacal Research
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• v.14 no.4
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• pp.357-358
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• 1991

Two flavonoids were isolated from the rhizomes of Belamcanda chinensis and identified as kanzakiflavove-2 and 2R:3R-dihydrokaempferol-7-methylether, respectively.

• Archives of Pharmacal Research
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• v.4 no.2
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• pp.133-135
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• 1981

Reaction of unsaturated acids with 3-bromo-5, 5-dimenthylhydantoin in dry DMF at room temperature gives bromolactones in 58-91 % yields.

• Archives of Pharmacal Research
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• v.4 no.2
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• pp.137-139
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• 1981

Reaction of olefinic acids with N-bromophthalimide in dry N, N-dimethylf-ormamide at room temperature gives bromolactones in good yields.

• Archives of Pharmacal Research
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• v.22 no.6
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• pp.624-628
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• 1999

A formal asymmetric synthesis of Mugineic acid was accomplished from cis-2-butene-1,4-diol throughcatalytic Sharpless epoxidation oxidations and doupling reaction.

• Archives of Pharmacal Research
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• v.29 no.6
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• pp.476-478
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• 2006

In order to construct a benzofuran library, we developed a model study of benzbromarone. Synthesis has been achieved in 53% overall yield, starting from phenol via the key intermediate 2-ethylbenzofuran which was afforded by intramolecular Wittig reaction.

• Archives of Plastic Surgery
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• v.47 no.1
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• pp.110-113
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• 2020

• Archives of Pharmacal Research
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• v.12 no.1
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• pp.34-38
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• 1989

Papaverine administration produced significant increases in acetylcholinesterase activity in cerebral cortex and striatum of rat brain. Two related compounds, tetrahydropapaverine and tetrahydropapaveroline, also gave similar effects. However, their actions seem to be indirect because papaverine has no in vitro effect on the enzymatic activity.

• Archives of Pharmacal Research
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• v.6 no.1
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• pp.25-28
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• 1983

From the stem bark of Albizzia julibrissin (Leguminosae) two known sapogenins, acacigenin B, and machaerinic acid lactone, were isolated and identified by chemical and spectral data. It is the second time that the former was isolate dform the plant sources.

• Archives of Pharmacal Research
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• v.8 no.3
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• pp.133-137
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• 1985

The aglycones of saponins isolated from Melandrium firmum were identified as gypsogenin, gypsogenic acid and quillaic acid.

• Archives of Pharmacal Research
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• v.16 no.2
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• pp.152-154
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• 1993

By using N-bromophthalimide (NBP) as halonium ion source for the Hofmann rearrangement, a series of primary amide could be ocnverted to the corresponding cabamate in excellent yields. So NBP was throught to be very effective and practical halonium ion source for the Hofmann rearrangement.