• Bulletin of the Korean Chemical Society
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• v.31 no.8
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• pp.2135-2136
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• 2010

• Bulletin of the Korean Chemical Society
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• v.30 no.11
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• pp.2823-2824
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• 2009

• Proceedings of the PSK Conference
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• 2003.04a
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• pp.239.2-240
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• 2003

We have recently described the novel synthetic method for N-protected amines from various ethers using chlorosulfonyl isocyanate(CSI) and found that the mechanism of our CSI reaction is a competitive reaction of SN1 and SNi mechanism according to the stability of carbocation intermediate. Forthermore. we developed the regioselective and diastereoselective one-pot synthetic method for 1,2-amino alcohol, through the reaction of di-and tribenzyl thers with CSI, and invetigated its mechanism. (omitted)

• Bulletin of the Korean Chemical Society
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• v.34 no.6
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• pp.1741-1744
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• 2013

A new polymeric catalyst was prepared by supporting $GaCl_3$ on cross-linked polyvinylpyrrolidone ($GaCl_3$/PVP). This catalyst was employed for efficient and regioselective ring-opening reaction of epoxides by various alcohols under solvent-free conditions at room temperature. In our procedure, this heterogeneous catalyst was used at neutral and mild reaction conditions to afford high yields of ${\beta}$-alkoxy alcohols. Also, regioselective conversion of epoxides to ${\beta}$-azidohydrines was accomplished by sodium azide in MeOH in the presence of $GaCl_3$/PVP at room temperature. $GaCl_3$/PVP is a non-hygroscopic and recoverable catalyst and is easily separated from reaction mixture by a simple filtration and re-used repeatedly. Also, this catalyst has good handling and can be stored for long time without any reducing of its reactivity.

• Bulletin of the Korean Chemical Society
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• v.33 no.9
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• pp.2890-2896
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• 2012

A simple regioselective synthesis of cinnoline derivatives was achieved by a one-pot three component synthetic methodology. New substituted 7,8-dihydrocinnolin-5(6H)-ones are prepared via one-pot three component reaction of arylglyoxals with 1,3-cyclohexanedione and dimedone in the presence of hydrazine hydrate in moderate to good yields.

• Bulletin of the Korean Chemical Society
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• v.35 no.12
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• pp.3675-3678
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• 2014

• Bulletin of the Korean Chemical Society
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• v.16 no.12
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• pp.1208-1212
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• 1995

A 86:14 isomeric mixture of 3,4-[3'-(dichlorosilyl)isopropyl]benzo-1,1-dichloro-1-silacyclopentene and 3,4-[2'-(dichlorosilyl)isopropyl]benzo-1,1-dichloro-1-silacyclopentene was prepared by the regioselective Friedel-Crafts reaction of allyldichlorosilane with 3,4-benzo-1,1-dichloro-1-silacyclopentene catalyzed by Lewis acid AlCl3. The structure of the products was confirmed by methylation with methylmagnesium bromide and by methoxylation with trimethylorthoformate.

• Bulletin of the Korean Chemical Society
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• v.29 no.2
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• pp.301-302
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• 2008

• Journal of the Korean Chemical Society
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• v.48 no.4
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• pp.443-446
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• 2004

• Bulletin of the Korean Chemical Society
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• v.20 no.12
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• pp.1384-1386
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• 1999