• 한국환경독성학회:학술대회논문집
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• 한국환경독성학회 2003년도 춘계학술대회
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• pp.145-145
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• 2003

A method for the determination of alkylphenols, chlorophenols and bisphenol A in paper materials using GC/MS-SIM has been developed. Eleven endocrine disrupting chemicals (EDCs) of phenols in paper samples were extracted with acetonitrile. Also, solid-phase extraction (SPE) with XAD-4 and subsequent conversion to isobutoxycarbonyl derivatives or tert.-butyldimethylsilyl derivatives for sensitive analysis with the selected ion-monitoring (SIM) mode. The recoveries were 82.4∼108.8 % by area ratio of pheranthrene-d$\sub$10/ vs bisphenol A d$\sub$l6/. (isoBOC derivatization and TBDMS derivatization) The SIM responses were linear with the correlation coefficient varying 0.9717∼0.9995 (isoBOC derivatization), and 0.9842∼0.9980 (TBDMS derivatization). The range of concentrations was respectively, 0.95∼l.44 ng/g in 2,4-dichlorophenol, 1.01∼1.17 ng/g in t-butylphenol, 2.17∼5.84 ng/g in pentachlorophenol, 12.68∼14.88 ng/g in nonylphenol and 30.84∼153.72 ng/g in bisphenol A.

• Macromolecular Research
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• 제11권1호
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• pp.69-72
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• 2003

A homopolymer having pendent t-Boc-protected quinizarin moieties has been prepared for patterned fluorescence images. The homopolymer P(t-BQN (2-norbornenylmethyl di-tert-butoxycarbonylquinizarin)) 5 was prepared by palladium-catalyzed addition polymerization. The t-Boc-protecting groups of the polymer were efficiently removed during chemical amplification process and revealed original properties of quinizarin, allowing patterned fluorescence images in the polymer film.

• Bulletin of the Korean Chemical Society
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• 제12권1호
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• pp.71-74
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• 1991

Facile methods are reported for the synthesis of optically pure derivatives of (2S,3R)-3-amino-2-hydroxy-4-(4'-hydroxyphenyl)b utanoic acid. To avoid troublesome synthesis of O-benzyl-N-Boc-D-tyrosine, without the protection of phenolic OH group of tyrosine N-Boc-D-tyrosine methyl ester was reduced with DiBAL to the aldehyde. The aldehyde was converted via the cyanohydrin to (2S,3R)-3-amino-2-hydroxy-4-(4'-hydroxyphenyl)butanoic acid (AHpHBA). The mixture of diastereomers was converted to the corresponding Boc-AHpHBA methyl ester derivatives and separated by chromatography over silica gel. Optically active (2S,3R)-AHpHBA was used to synthesize aminopeptidase inhibitors.

• Archives of Pharmacal Research
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• 제24권6호
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• pp.503-507
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• 2001

trans-Metanicotine, a subtype (${\alpha}_4{\beta}_2$)-selective ligand for neuronal nicotinic acetylcholine receptor, is under clinical phase for Alzheimer's disease. An efficient synthetic route for ($\pm$)-methyl-(1-aryl-4-pyridin-3-yl-but-3-enyl)-am ices, derivatives of tracts-metanicotine, was explored. Allylation reaction of aryl aldimines with allylmagnesium bromide in THF gave ($\pm$)-methyl-(1-aryl-but-3-enyl)-amines. Protection of the amines with the Boc group and following Heck reaction of the N-Boc amines with 3-bromopyridine gave ($\pm$)-methyl-(1-aryl-4-pyridin-3-yl-but-3-enyl)-carbamic acid tert-butyl esters. Deprotection of the N-Boc group in aqueous 1 N-HCI solution gave the titled amines in good yields. Thus, trans-metanicotine analogues modified at the ${\alpha}-position$ of the methylamino group with amyl groups were obtained in 5 steps.

• 한국통신학회논문지
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• 제33권1C호
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• pp.86-93
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• 2008

Galileo 시스템은 통신 물리계층으로 직접수열/대역확산(direct sequence/spread spectrum, DS/SS) 시스템을 사용한다. DS/SS 시스템은 수신신호로부터 정보를 복원하기 위해 수신신호의 확산신호와 수신기에서 발생한 확산신호의 동기를 정확하게 결정하고, 유지해야 한다. 이를 위해 DS/SS 시스템은 획득과 추적 단계를 수행해 동기를 맞춘다. 이상적인 환경에서 최적 부호추적기는 EL-DLL이다(delay lock loop with early minus late discriminator). EL-DLL은 정확한 동기시점을 기준으로 확산신호의 상관함수가 정확히 대칭인 특징을 이용해 추적을 수행한다. 그러나 다중경로 신호가 수신되었을 때 상관함수의 대칭성이 왜곡되며, 이로 인해 추적이 완료되어 동기시점을 결정한 후에도 일정한 동기오차가 존재한다. 이처럼 추적기가 동기시점을 결정한 후에도 잔존하는 동기오차를 추적편이라 한다. 이상적인 환경에서 Galileo BOC(1,1) 신호로 변조된 확산신호는 정확한 동기시점에서 최고 값이 나타나며, 이 시점을 기준으로 반 칩(chip) 이른 상관시간 옵셋과 늦은 상관시간 옵셋에서 극소 값을 갖는다. 이때 다중경로신호는 항상 가시신호에 비해 늦게 수신되기 때문에 정확한 동기시점을 기준으로 반 칩 이른 상관 시간 옵셋 주변의 상관 값은 다중경로신호에 의해 크게 왜곡되지 않는 특징을 갖는다. 본 논문은 이 특징을 바탕으로 Galileo BOC(1,1)에 알맞은 추적편이 완화기법을 제안하고, 기존 기법과 제안한 기법의 추적편이 특성을 분석한다.

• Macromolecular Research
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• 제12권6호
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• pp.615-617
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• 2004

We have developed an efficient method for the generation of patterned fluorescence images using a protected precursor molecule. The t-Boc-protecting group of a coumarin derivative was readily removed from a polymer film upon irradiation with UV light in the presence of a photoacid generator to provide the original properties of the coumarin. Fine fluorescence patterns were obtained when using this photolithographic method.

• Bulletin of the Korean Chemical Society
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• 제32권4호
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• pp.1195-1200
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• 2011

The catalytic enantioselective Mannich-type reaction promoted by chiral binaphthyl-modified bifunctional organocatalysts is described. The treatment of ${\alpha}$-fluoro-${\beta}$-ketoesters with N-Boc imines under mild reaction conditions afforded the corresponding ${\beta}$-aminated ${\alpha}$-fluoro-${\beta}$-ketoesters with excellent enantioselectivities (up to 98% ee).

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 1996년도 춘계학술대회
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• pp.163-163
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• 1996

Peptide 유도체, 특히 tyrosine을 함유한 peptide 유도체는 항암제 개발을 위한 연구의 관심이 되고 있다. Thiophosphotyrosine을 함유한 peptide는, 종양 발현에 관련되는 여러 효소의 억제제로써, 즉 protein tyrosine kinase(PTK)의 억제제 및 protein tyrosine phosphatase(PTPase)의 억제제 혹은 cytosolic protein의 결합을 방지하는 차단제로 사용할 수 있으며 궁극적으로 항암제 개발에 응용할 수 있다. 이에, t-BOC chemistry를 이용하여 t-BOC-tyrosine을 출발물질로 하고, cyanoethyl 기를 phosphate protecting group으로 사용하여 thiophosphotyrosine을 함유한 peptide 유도체의 합성에 필요한 중요한 중간체 인 N-(tert-butoxycarbonyl)-O-(dicyanoethylthio-phosphene)-L-tyrosine을 합성하였다.

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.235.2-236
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• 2002

The alkylphenols, chlorophenols and bisphenol A were determined by gas chromatography/mass spectrometry-selected ion monitoring mode followed by three work-up methods for comparison: EPA method, isoBOC derivatization method and TBDMS derivatization method. Eleven phenols in water samples were extracted with dichloromethane. (omitted)

• Archives of Pharmacal Research
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• 제21권3호
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• pp.330-337
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• 1998

N-(tert-Butoxycarbonyl)-O-(dimethythiophosphono)-L-tyrosine (6) and N-(tert-butoxycarbonyl)-O-(dicyanoethylthiophosphono)-L-tyrosine (15) were prepared as intermediates for the synthesis of thiophosphotyrosine-containing peptides. The reactivity and suitability of two compounds for the solid phase or solution phase peptide synthesis utilizing t-Boc chemistry were examined.