• 대한화학회지
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• 제52권1호
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• pp.52-56
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• 2008

제법을 위한 쉽고 효과적인 이 방법은 solvent-free하에서 H3PMo12O40 촉매를 사용해서 개선되었다. 이 방법의 큰 이점은 조작의 간편성, 더 작은 촉매량, 선택성, 온화한 반응조건,짧은 반응 시간 그리고 높은 수율이다. 재생된 촉매는 어떤 정제도 없이 다시 사용되어질 수 있다.

• Bulletin of the Korean Chemical Society
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• 제26권11호
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• pp.1689-1691
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• 2005

1-Butyl-4-aza-1-azoniabicyclo[2.2.2]octane dichromate (BAABOD) 3 is a useful reagent for the selective cleavage of trimethylsilyl ethers and tetrahydropyranyl ethers to their corresponding aldehydes and ketones in the presence of $AlCl_3$ under solvent-free conditions. This method is very simple and efficient and the reaction has been carried out under solvent-free conditions in the presence of a catalytically amount of aluminum chloride.

• Bulletin of the Korean Chemical Society
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• 제32권5호
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• pp.1575-1578
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• 2011

Antimony trichloride (SbCl3) was demonstrated to be an effective catalyst for the cyanosilylation of a wide variety of carbonyl compounds under solvent-free conditions. The reactions proceeded smoothly at room temperature to afford the corresponding cyanosilylethers in good to excellent yields.

• Bulletin of the Korean Chemical Society
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• 제32권4호
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• pp.1179-1182
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• 2011

In the present work, successful implementation of ultrasound irradiations for the rapid synthesis of 1,5-benzodiazepine derivatives under solvent-free conditions is demonstrated. Use of a novel catalyst i.e. camphor sulphonic acid in combination with ultrasound technique is reported for the first time. Comparative study for the synthesis of 1,5-benzodiazepines using conventional as well as ultrasonication method is discussed.

• Bulletin of the Korean Chemical Society
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• 제32권4호
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• pp.1201-1203
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• 2011

A one-pot conversion of tertiary thioamides to S-2-oxo thioesters is reported. Hence, tertiary thioamides were reacted with ${\alpha}$-halo ketones or acids under solvent-free conditions to produce the corresponding oxo-thioesters in good to excellent yields.

• Bulletin of the Korean Chemical Society
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• 제32권12호
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• pp.4297-4303
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• 2011

Under solvent-free conditions, the synthesis of propargylic alcohols by direct addition of terminal alkynes to aldehydes promoted by ZnO as a novel, commercially, and cheap catalyst is described. Furthermore, the catalyst can be reused for several times without any significant loss of its catalytic activity.

• Bulletin of the Korean Chemical Society
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• 제30권8호
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• pp.1767-1770
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• 2009

The Henry (nitroaldol) reaction proceeds under mild conditions with catalytic amount of tetramethylethylenediamine (TMEDA) to afford $\beta$-nitro alkanol in considerably excellent yield. Structurally diverse aldehydes react with nitromethane in presence of 0.3 equiv of TMEDA under solvent-free condition at rt. The low catalytic loading and mild reaction condition are the key features of the catalytic method.

• Bulletin of the Korean Chemical Society
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• 제25권2호
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• pp.325-327
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• 2004

• Bulletin of the Korean Chemical Society
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• 제26권9호
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• pp.1331-1332
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• 2005

• Bulletin of the Korean Chemical Society
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• 제32권7호
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• pp.2482-2484
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• 2011