• The Korean Journal of Mycology
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• v.17 no.4
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• pp.202-208
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• 1989

The photochemical reaction of harmaline and N-methylmaleimide has been investigated by spectroscopic methods. A photoproduct was isolated from the irradiation mixture of harmaline and N-methylmaleimide. Spectroscopic results suggested that the amine group of harmaline was added photochemically to the double C=C bond of N-methylmaleimide. This synthesized harmaline derivative has a biological toxicity, because it inhibits the growth of some yeasts and photosynthetic bacteria.

• The Korean Journal of Pesticide Science
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• v.10 no.1
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• pp.1-6
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• 2006

A methodology for the syntheses of carboxanilides using solid support of 4-chloro-3-nitorbenzophenone oxime resin 5 was developed. Condensation of 4-chloro-3-nitorbenzophenone resin 6 with hydroxylamine hydrochloride salt gave oxime resin 5. The reaction of oxime resin 5 with dioxin and oxathiin derivatives 7a-d afforded the corresponding polymer-bound dioxin and oxathiin derivatives 9a-d. These polymer-bound resins 9a-d were treated respectively with aniline in the presence of acetic acid resulted in the corresponding dioxin carboxanilides 10a-d (yield, 5%-quantitative).

• Journal of the Korean Chemical Society
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• v.27 no.6
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• pp.449-456
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• 1983

The facile route of preparing S-2-(${\omega}$-aminoalkylamino) ethyl dihydrogen phosphorothioates, potential chemical radioprotectants, have been studied. Intermediate 3-(2-phthalimidoethyl)-2-oxazolidinone was prepared by a reaction of potassium phthalimide and 3-(2-bromoethyl)-2-oxazolidinone, which was obtained through the alkaline ring closure of a mixture of carbonate and 2,2'-dibromo diethylamine prepared from diethanolamine. This was converted to N-[2-(2-bromoethylamino)ethyl] phthalimide hydrobromide by 30% HBr(gas) in acetic acid and N-(2-bromoethyl)-1,2-ethanediamine dihydrobromide was obtained by reacting the hydrobromide with a solution of HBr-HOAc. N-(2-bromoethyl)-1,3-propanediamine dihydrobromide could be prepared through the Cortese treatment of 2-(3-aminopropylamino) ethanol, which was prepared by a reaction of 1,3-diaminopropane and 2-chloroethanol. These dihydrobromides were treated by sodium thiophosphate in DMF to result S-2-(${\omega}$-aminoalkylamino) ethyl dihydrogen phosphorothioates. The characteristics of each reaction path were discussed in regards to reaction conditions and overall yields and a facile route of preparing each derivative was proposed.

• Journal of the Korean Chemical Society
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• v.40 no.8
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• pp.571-578
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• 1996

Iron alkynyl(amino)carbene complexes, (${\beta}$-aminovinyl)carbene complexes, ${\eta}^3$-(2-(alkylcarbonyl)vinyl)carbene complexes, and a 3-aminoallenylidene complex were formed in the reactions of iron alkynyl(ethoxy)carbene complexes with amines. The ratio of the products, which were formed by substitution reaction, the Michael addition of amines, rearrangements after the addition reaction, and the addition followed by the elimination of the ethoxy group, respectively, was dependent on reaction temperature, the substituent of the alkynyl moiety, and employed amines.

• Journal of the Korean Chemical Society
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• v.51 no.3
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• pp.244-250
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• 2007

A series of new 6-allylthio-3-aminopyridazine derivatives was synthesized through allylthiolation, amination and expected for anti-tumor activity. The pyridazine nucleus was obtained by condensing hydrazine monohydrate with maleic anhydride. 3,6-Dichloropyridazine was synthesized from 3,6-dihydroxypyridazine by treating with POCl3. 6-Allylthio-3-chloropyridazine was prepared from the reaction of 3,6-dichloropyridazine with allylmercaptan and sodium hydroxide. The heterocycles with nitrogen nucleophile such as morpholine, piperazine, pyrazole, imidazole, pyrrolidine, piperidine, perhydroazepine, and perhydroazocine were introduced into 3-position of pyridazine ring. The substitution reaction of 6-allylthio-3-chloropyridazine with heteroamines was performed by refluxing for 24~48 h in n-buthanol with NH4Cl.

• Korean Journal of Environmental Agriculture
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• v.8 no.2
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• pp.136-141
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• 1989

An alternative method for the synthesis of sulfonylurea derivatives, some of which considered to be a new recommendable herbicides, with oxalylchloride was investigated. Sulfonamides read with oxalylchloride to sulfonyloxamoylchlorides, which convert easily under pyrolysis to sulfonylisocyanates. The isocyanates react further with amines to yield corresponding sulfonylurea derivative quantitatively.

• Proceedings of the Korean Fiber Society Conference
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• 1998.04a
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• pp.338-341
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• 1998

악취의 주원인은 염기성 취기의 대표인 암모니아, 산성 취기의 대표인 황화수소, 그리고 트리메틸아민이며, 이들은 법정 악취물질로써 지정되어 있다$^1$. 이와 같은 악취를 없애는 소취기구는 활성탄 및 제오라이트 등과 같은 물질에 대한 물리적 흡착에 의한 것, 산화제 및 환원제에 의한 화학반응에 의한 것, 미생물 및 효소에 의한 생물학적 반응에 의한 것으로 대별되지만, 물리 흡착은 재방출의 문제가 있고 화학 및 생물학적 반응에는 소취성분 자체의 유해성 및 반응후 물질의 유해성이 문제가 되는 경우가 있다.(중략)

• Journal of the Korean Chemical Society
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• v.44 no.1
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• pp.45-51
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• 2000

The binding mode of anthryl derivatives to synthetic polynucleotides were investigated by various spectroscopic methods. The spectroscopic properties of anthracence with metbylamine and methylethylenediamine side chains, complexed with $poly[d(A-T)_2]$ and $poly[d(G-C)_2]$, can be summarized as a red-shift, with a strong hypochromism in the absortion spectrum, similar induced CD spectra, and a strong negative LD spectrum with an $LD^r$ magnitude comparable to the DNA absorption region. These observations indicate that anthracene moiety is intercalated between the nucleo-bases of $poly[d(A-T)_2]$ and $poly[d(G-C)_2]$. The side chains did not alter the spectroscopic properties, demonstrating that the binding mode was not affected by them. A strong energy transfer was observed from poly[d(A-T),] and $poly[d(I-C)_2]$ but not from $poly[d(G-C)_2]$, as reported by Kumar et al. (J. Am. Chem. Soc.(1993) 115, 8547). Since the binding mode is the same for all the polynucleotides, the amine group of the guanine base, which protrudes into the minor groove of $poly[d(G-C)_2]$, is concluded to disrupt the energy transfer.

• Journal of the Korean Applied Science and Technology
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• v.12 no.2
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• pp.41-50
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• 1995

2염기성 산의 모노메틸에스테르류와 에틸렌디아민을 반응시켜 얻은 아미도아민 유도체류를 고급지방산 염화물로 아실화하여 N-아실 아미도에틸 N-아미도카르복시산 유도체 9종을 합성하였다. 카르복시기와 디아미드기 그리고 소수성의 긴 알칼사슬을 갖는 모든 반응생성물들은 얇은 막 크로마토그래피와 컬럼크로마토그래피로 분리 ${\cdot}$ 정제하였다. 합성 수율은 $74{\sim}87%$였으며 그들의 구조를 FT-IR, $^1H-NMR$, 그리고 원소 분석으로 확인하였다.

• Journal of the Korean Chemical Society
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• v.20 no.4
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• pp.295-298
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• 1976

The fact that a reaction between organothioenamine phosphonate and styrene oxide produces a derivative of cyclopropane has been proved by structural identification. This suggests that an anionic oxygen atom from the ring opening of the styrene oxide by nucleophilic attack of thioenamine phosphonate links to the phosphorous atom to from a betaine as an intermediate which is followed by cleavage of the weak P-C bond. The dextrorotatory optical activity of the product showed that the reaction was under the control of steric stability of the benzyl carbon in styrene which leads to the product through a sterically stable pathway.