• 대한화학회지
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• 제52권1호
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• pp.52-56
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• 2008

제법을 위한 쉽고 효과적인 이 방법은 solvent-free하에서 H3PMo12O40 촉매를 사용해서 개선되었다. 이 방법의 큰 이점은 조작의 간편성, 더 작은 촉매량, 선택성, 온화한 반응조건,짧은 반응 시간 그리고 높은 수율이다. 재생된 촉매는 어떤 정제도 없이 다시 사용되어질 수 있다.

• Bulletin of the Korean Chemical Society
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• 제9권5호
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• pp.322-324
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• 1988

Selective reduction of aldoximes and ketoximes with lithium borohydride in tetrahydrofuran was investigated. Thus, aldoximes and cyclic ketoximes such as hexanaldoxime, heptanaldoxime, cyclopentanone oxime and cyclohexanone oxime were reduced smoothly to the corresponding N-monosubstituted hydroxylamines at room temperature in 65-93% yield. The reduction of alicyclic ketoxime was very slow, requiring somewhat high reaction temperature ($65^{\circ}C$) for the complete reduction to give the hydroxnylamines. The reduction of aromatic oximes such as benzaldoxime and acetophenone oxime was very sluggish, giving a mixture of the corresponding hydroxylamines and amines at $65^{\circ}C$.

• Bulletin of the Korean Chemical Society
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• 제33권10호
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• pp.3173-3174
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• 2012

• Bulletin of the Korean Chemical Society
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• 제28권1호
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• pp.29-30
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• 2007

• Bulletin of the Korean Chemical Society
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• 제29권12호
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• pp.2496-2498
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• 2008

• Bulletin of the Korean Chemical Society
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• 제33권6호
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• pp.2102-2104
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• 2012

• Bulletin of the Korean Chemical Society
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• 제8권6호
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• pp.466-470
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• 1987

Di-2-pyridyl thionocarbonate, prepared from thiophosgene and 2-hydroxypyridine in the presence of triethylamine in dichloromethane, was found to be very effective for dehydration, dehydrosulfurization, and thiocarbonyl transfer reactions. Di-2-pyridyl thionocarbonate was successfully for the esterification of carboxylic acids, dehydration of aldoximes into nitriles, preparation of isothiocyanates from amines, and preparation of cyclic thionocarbonates from 1,2- and 1,3-diols.

• Bulletin of the Korean Chemical Society
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• 제32권9호
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• pp.3323-3326
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• 2011

Various aldoximes and ketoximes were efficiently reduced to their corresponding amines with $NaBH_3CN$ in the presence of $MoCl_5/NaHSO_4{\cdot}H_2O$ system. Reduction reactions were carried out in refluxing EtOH or DMF within 0.3-3.8 h to afford the amines in high to excellent yields.

• Bulletin of the Korean Chemical Society
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• 제32권9호
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• pp.3448-3452
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• 2011

Solvent-free reduction of various aldoximes and ketoximes to the corresponding amines was performed easily and efficiently with $NaBH_4$ in the presence of $ZrCl_4$ supported on $Al_2O_3$. The reactions were carried out rapidly (within 2 min) at room temperature to afford the amines in high to excellent yields.