• Bulletin of the Korean Chemical Society
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• 제8권3호
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• pp.211-214
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• 1987

Asymmetric reduction of a series of aliphatic ketones and representative other classes of ketones with potassium 9-O-isopinocampheyloxy-9-boratabicyclo[3.3.1]non ane (K 9-O-Ipc-9-BBNH) was studied. All the ketones examined were reduced smoothly to the corresponding alcohols in THF at -$78^{\circ}C$. Thus, the reduction of 2-butanone, 3-methyl-2-butanone, 3,3-dimethyl-2-butanone, 2-octanone, and 4-phenyl-2-butanone provides 51% ee, 61% ee, 44% ee, 35% ee, and 33% ee of optical inductions, respectively. The reduction of other classes of ketones gave 52% ee for 2,2-dimethylcyclopentanone, 47% ee for acetophenone, 23% ee for 3-acetylpyridine, 50% ee for methyl benzoylformate, 4.8% ee for 2-chloroacetophenone, 30% ee for trans-4-phenyl-3-butene-2-one, and 2% ee for 4-phenyl-3-butyn-2-one. Thus, the reagent was found to be most useful in the asymmetric reduction of acyclic and cyclic aliphatic series of ketones.

• 대한화학회지
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• 제26권5호
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• pp.296-303
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• 1982

수용액 속에서 1-페닐-2-아세트아미도-3-부탄온의 용해도를 20, 30, 40$^{\circ}$C 에서 또 1kg/$cm^2$에서 4500 kg/$cm^2$까지의 압력에서 측정하였다. 압력이 커질수록 용해도는 감소한다. 이러한 용해도 변화는 디케토피페라진과 아주 비슷하다. 디케토피페라진이 펩타이드 결합의 모델 화합물이라는 점과 1-페닐-2-아세토아미도-3-부탄온이 한개의 펩타이드 결합과 상당히 큰 소수성 작용기를 가졌다는 점을 고려할 때 이와 같은 용해도 변화는 예상 밖이다. 부피 변화와 열용량 변화에 대한 값은 이상하다고 할 정도는 아니었다.

• 생약학회지
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• 제16권3호
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• pp.136-140
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• 1985

Sixty-eight kinds of aliphatic and aromatic substances peaks from ether extract of Codonopsis pilosulae Radix were shown by GC-Mass. Of them, 3 kinds of compounds were identified as ethyl benzene, acetophenone and 1-phenyl-2-butanone, which are compared with authentic specimen, and one compound was assumed as an aliphatic $C_8H_{16}O\;or\;C_9H_{20}$.

• 약학회지
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• 제29권4호
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• pp.183-187
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• 1985

During investigation of the anthelmintic substances against Clonorchis sinensis which are based on the structure of meso-dihydroguairaretic acid, some non-mesoic diaryl butanes were synthesized by Grignard reaction and their anthelmintic activities were determined. In this reaction, an aryl butanone was reacted with benzylmagnesium chloride to produce the corresponding diaryl hydroxybutane which was converted to the corresponding diaryl butane by zinc and hydrogen chloride. The substituents in benzene ring of the diaryl butanes were changed by methylation or demethylation. Among the synthesized substances, 4-phenyl-1-(3, 4-dihydroxyphenyl)-2, 3-dimethylbutane(VII), 4-phenyl-1-(3-hydroxy-4-methoxyphenyl)-2, 3-dimethylbutane(IX) and 4-phenyl-1-(4-hydroxy-3-methoxyphenyl)-2, 3-dimethylbutane(VI) showed strong wormicidal effects against Clonorchis si-nensis in that order. Phenolic hydroxyl group seemed to play a certain role for the wormicidal activity of the diaryl butanes.

• Journal of the Korean Wood Science and Technology
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• 제30권4호
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• pp.80-86
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• 2002

졸참나무 (Quercus serrata), 맹종죽 (Phyllostachys pubescens) 및 소나무 (Pinus densiflora)로부터 제조한 미정제 초액의 휘발성 성분을 고상(固相) 미량추출(solid phase microextraction; SPME)법을 이용하여 분석하였다. 이들 초액 중의 휘발성화합물 분석을 위하여 극성 (CBP 20) 및 무극성 (CBP 1) 칼람을 사용하였으며, 이로부터 총 264개의 피크를 검출하였다. 이들 성분들 중 주요 화합물은 2-butanone, acetic acid, guaiacol, phenol, 4-ethyl guaiacol, cresol류, 4-ethyl phenol, 그리고 syringol이었다. 무극성 칼람을 사용함에 의하여 7개의 성분, 즉, 1-hydroxy-2-butanone, ethisolide, furfuryl acetate, 1-(2-furanyl)-1-propane, 1,2-dimethoxybenzene, 1,2-dimethoxybenzyl alcohol, phenyl acetate를 새로이 동정할 수 있었다. 이 성분들 중 페놀류가 주성분이었으며, 휘발성 성분의 49~65%를 차지하였다. 죽초액의 경우 페놀류의 비율은 다른 두 목초액보다 낮았다. 그러나 중성화합물류 및 유기산류는 소나무 및 졸참나무로부터 제조한 목초액보다 그 비율이 더 높았다. 따라서 이들 죽초액과 목초액 간의 훈취의 차이는 목초액의 서로 다른 휘발성분의 함유량의 차이에 기인한다고 생각된다.