• Archives of Pharmacal Research
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• 제23권6호
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• pp.574-578
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• 2000

Protected $\alpha$-Phenyl glycine 17 and phenylalanine 18 and 19 have been synthesized through an efficient three-step sequence from the corresponding allyl ethers 5, 7, and 10. The key intermediate in this synthesis is the corresponding allylic amines prepared by reaction of allyl ethers with chlorosulfonyl isocyanate.

• 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.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)

• 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)

• Elastomers and Composites
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• 제54권2호
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• pp.128-134
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• 2019

Many scientific approaches have been developed for the preparation of alternative crosslinker system of amino resins and isocyanate prepolymers. Herein, copolymerization of trimethoxy silane with N-butoxymethyl acrylamide was performed, and the product was reacted with hydroxyl groups in the alkyl main chain without the need for an additional crosslinker. For the crosslinker synthesized herein, the molecular weight, glass transition temperature, and viscosity increased with increasing content of N-butoxymethyl acrylamide.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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• pp.183.1-183.1
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• 2003

The synthesis of various cyclic carbamate compounds and amino alcohols has attracted attention in the past because of their potential as antibiotics, antitumor, analgenics, anticonvulsants. Several methods for the preparation of cyclic carbamate compounds have previously been reported including the use of heterocumulenes. 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 $S_N1$ and $S_ Ni$ mechanisms according to the stability of carbocation intermediates. (omitted)

• 월간산업보건
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• 통권144호
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• pp.45-47
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• 2000

• 월간산업보건
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• 통권145호
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• pp.19-21
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• 2000

• 월간산업보건
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• 통권146호
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• pp.30-31
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• 2000

• Korean Chemical Engineering Research
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• 제48권5호
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• pp.568-573
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• 2010

본 연구에서는 polyester 섬유표면에 활성기를 부여하기 위한 전처리제로 isocyanate를 이용하여 농도에 따른 접착력을 평가하였다. 이 후 HNBR compound와 polyester fabric의 접착 시 접착력이 우수한 RFL 용액용 latex 선정 및 F/R mole ratio, F/R resin/latex 무게 비에 따른 실험을 진행하였다. 그 결과 전처리제의 농도가 7 wt%인 경우 가장 높은 접착력을 나타내었으며, RFL 용액용 latex로는 HNBR 컴파운드와 상용성이 높은 NBR latex가 우수한 결과를 나타내었고 F/R mole ratio, FR resin/latex 무게비가 각각 1/1, 20%일 때 가장 높은 접착력을 나타내었다. 또한, peel test와 FTIR 분석을 이용해 RF resin의 열처리 온도에 따른 접착강도와 spectra의 peak 변화를 평가해 본 결과 최적의 열처리 온도는 $200^{\circ}C$이었다.

• Journal of the Korean Wood Science and Technology
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• 제28권1호
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• pp.36-41
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• 2000

목재는 2-메타크릴로일옥시에틸 이소시아네이트(MOI)와 $50-60^{\circ}C$에서 촉매존재하에서 매우 쉽게 반응하였다. 적외선 분광분석을 통하여, 목재가 MOI와 우레탄결합($1715cm^{-1}$)를 형성하고 있을 뿐만 아니라, 올레핀구조의 탄소간 이중결합 ($1635cm^{-1}$)이 존재하고 있음이 밝혀졌다. 도입된 메타크릴산기는 다른 비닐모노머와의 그래프트공중합시 반응시점으로 작용할 것이다. 또한 MOI처리목재는, MOI와의 반응에 의해 친수성이던 목재의 표면이 소수화되어 접촉각이 증대되는 결과를 낳았다. X선광전자분광분석(XPS)의 결과, 목재의 표면부위의 대부분은 MOI에 의해 개질되었음을 밝혀졌다.