• Bulletin of the Korean Chemical Society
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• 제34권11호
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• pp.3503-3506
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• 2013

• Bulletin of the Korean Chemical Society
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• 제24권3호
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• pp.267-268
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• 2003

• 대한화학회지
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• 제50권4호
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• pp.346-350
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• 2006

• Bulletin of the Korean Chemical Society
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• 제28권4호
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• pp.624-628
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• 2007

Synthesis of 4-substituted 3-exo-methylenechroman derivatives was carried out by the n-Bu3SnH-mediated vinyl radical cyclization as the key step starting from various salicylaldehydes.

• Archives of Pharmacal Research
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• 제22권4호
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• pp.391-397
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• 1999

The quaternary ammonium cephalosporin derivatives were prepared with various pyridines substituted at the 3 or/and 4 position. Their in vitro antibacterial activities were determined and substituent effect on pyridine nucleus was studied. Preparation of substituted pyridines are also described.

• Archives of Pharmacal Research
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• 제20권2호
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• pp.158-170
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• 1997

New HMG-CoA reductase inhibitors, in which 3-substituted 4, 5-polymethylenepyrazoles are employed as a hydrophobic anchor connected to tetrahydro-4-hydroxy-2H-pyran-2-one by a two-carbon bridge, were designed and synthesized to exhibit significant inhibitory activity comparable to mevinolin. The most potent enzyme inhibitor $(11cc, IC_{50}=0.01{\mu}M)$ is 4-fold more potent than lovastatin.

• 통합자연과학논문집
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• 제5권2호
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• pp.91-99
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• 2012

A newly-devised Meerwein-Ponndorf-Verley (MPV) reagents, such as diisobutylacetoxyalanes and diisobutylmethanesulfonylalanes, achieved a clean conversion of unsymmetrical epoxides to the corresponding less substituted alcohols. This review covers the recent developments for such a regiospecific ring-opening reaction of epoxides.

• Bulletin of the Korean Chemical Society
• /
• 제25권12호
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• pp.1935-1936
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• 2004

• 대한화학회지
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• 제56권3호
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• pp.322-327
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• 2012

Rapid and efficient synthesis of substituted 3-carboxylquinoline derivatives from 4-chloro-3-formylcoumarin and substituted anilines using 30% $H_2SO_4$ in methanol at room temperature within the duration of 5-30 min., through domino condensation-cyclization-ring opening reaction.

• 대한화학회지
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• 제54권5호
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• pp.589-593
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• 2010

TBACl (10 mol %) 를 촉매로 사용하여 치환된benzimidazoles을 합성하는 간단하고 효율적인 합성방을 개발하였다.