• 대한화학회지
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• 제59권6호
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• pp.533-536
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• 2015

• Bulletin of the Korean Chemical Society
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• 제29권4호
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• pp.723-724
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• 2008

• Bulletin of the Korean Chemical Society
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• 제30권8호
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• pp.1877-1880
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• 2009

• Bulletin of the Korean Chemical Society
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• 제29권12호
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• pp.2445-2448
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• 2008

• Bulletin of the Korean Chemical Society
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• 제33권4호
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• pp.1371-1374
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• 2012

• Bulletin of the Korean Chemical Society
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• 제30권1호
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• pp.239-241
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• 2009

• Bulletin of the Korean Chemical Society
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• 제30권11호
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• pp.2833-2836
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• 2009

• Bulletin of the Korean Chemical Society
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• 제33권5호
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• pp.1556-1560
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• 2012

A simple highly versatile and efficient method has been developed for the three-component coupling of aldehydes, amines and alkynes to prepare propargylamines, in the presence of a catalytic amount of $BiCl_3$. The advantages of methods are high yield, mild reaction conditions, no environmental pollution and easy work up procedure.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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• pp.242.2-243
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• 2003

We have developed the novel one-pot synthetic method for regioselective N-protected amines, carbamates as a protective group of amines, through the reaction of various ethers with chlorosulfonyl isocyanate (CSJ). This synthetic method provides a simple and convenient alternative for the formation of carbamates, such as -NHMoc, -NHPoc. -NHCbz, -NHPnz, -NHTroc and -NHAloc, by varying the alkyl moiety of ethers. (omitted)

• Bulletin of the Korean Chemical Society
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• 제32권7호
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• pp.2203-2206
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• 2011

A mild and efficient procedure has been developed for the one-pot, three-component reaction of aldehydes, benzyl carbamate and allyltrimethylsilane in the presence of 3 mol % of magnesium bistrifluoromethanesulfonimide at room temperature to afford the corresponding protected homoallylic amines in high yields.