• 제목/요약/키워드: Chiral amine

검색결과 24건 처리시간 0.019초

Effect of dimensionless nonlocal parameter: Vibration of double-walled CNTs

  • Hussain, Muzamal;Asghar, Sehar;Khadimallah, Mohamed Amine;Ayed, Hamdi;Alghamdi, Sami;Bhutto, Javed Khan;Mahmoud, S.R.;Tounsi, Abdelouahed
    • Computers and Concrete
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    • 제30권4호
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    • pp.269-276
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    • 2022
  • In this paper, frequency vibrations of double-walled carbon nanotubes (CNTs) has been investigated based upon nonlocal elastic theory. The inference of small scale is being perceived by establishing nonlocal Love shell model. The wave propagation approach has been operated to frame the governing equations as eigen value system. An innovational nonlocal model to examine the scale effect on vibrational behavior of armchair, zigzag and chiral of double-walled CNTs. An appropriate selection of material properties and nonlocal parameter has been considered. The influence of dimensionless nonlocal parameter has been studied in detail. The dominance of end condition via nonlocal parameter is explained graphically. The results generated furnish the evidence regarding applicability of nonlocal shell model and also verified by earlier published literature.

[2-(diphenyl hydroxy-methyl)pyrrolidine]-AlH 유도체와 방향족 케톤의 선택적 환원에 대한 이론적 연구 (Theoretical Study on the Selective Reduction of Chiral [2-(diphenyl hydroxy-methyl)pyrrolidine]-AlH Derivatives and Aromatic Ketone)

  • 이철재;김종미
    • 문화기술의 융합
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    • 제7권2호
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    • pp.389-394
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    • 2021
  • 본 연구에서는 알콕시-아민-알루미늄 유도체인 DPHMP-AlH와 프로피오페논, 부티로페논과의 분자구조 및 경계궤도함수의 특성을 알아보았다. 또한, 전이상태의 입체구조 및 열역학적 파라미터를 계산하여 최종 생성물인 (R),(S)-페닐프로판올과 (R),(S)-페닐부탄올의 선택적 환원에 미치는 영향을 조사하였다. 그 결과 입체 분자구조적 안정성을 고려해 볼 때 (S)형 DPHMP-AlH와 알킬페논의 전이상태가 더 안정한 것으로 나타났으며, 이 결과로부터 DPHMP-AlH와 알킬페논의 선택적 환원으로 얻어진 최종 결과물은 (S)-(1)-페닐프로판올과 (S)-(1)-페닐부탄올의 형성이 유리한 것을 확인하였다.

R-Stereoselective Amidase from Rhodococcus erythropolis No. 7 Acting on 4-Chloro-3-Hydroxybutyramide

  • Park, Ha-Ju;Uhm, Ki-Nam;Kim, Hyung-Kwoun
    • Journal of Microbiology and Biotechnology
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    • 제18권3호
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    • pp.552-559
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    • 2008
  • Ethyl (S)-4-chloro-3-hydroxybutyrate is an intermediate for the synthesis of Atorvastatin, a chiral drug used for hypercholesterolemia. A Rhodococcus erythropolisstrain (No.7) able to convert 4-chloro-3-hydroxybutyronitrile into 4-chloro-3-hydroxybutyric acid has recently been isolated from soil. This activity has been regarded as having been caused by the successive actions of the nitrile hydratase and amidase. In this instance, the corresponding amidase gene was cloned from the R. erythropolis strain and expressed in Escherichia coli cells. A soluble active form of amidase enzyme was obtained at $18^{\circ}C$. The Ni column-purified recombinant amidase was found to have a specific activity of 3.89 U/mg toward the substrate isobutyramide. The amidase was found to exhibit a higher degree of activity when used with mid-chain substrates than with short-chain ones. Put differently, amongst the various amides tested, isobutyramide and butyramide were found to be hydrolyzed the most rapidly. In addition to amidase activity, the enzyme was found to exhibit acyltransferase activity when hydroxyl amine was present. This dual activity has also been observed in other enzymes belonging to the same amidase group (E.C. 3.5.1.4). Moreover, the purified enzyme was proven to be able to enantioselectively hydrolyze 4-chloro-3-hydroxybutyramide into the corresponding acid. The e.e. value was measured to be 52% when the conversion yield was 57%. Although this e.e. value is low for direct commercial use, molecular evolution could eventually result in this amidase being used as a biocatalyst for the production of ethyl (S)-4-chloro-3-hydroxybutyrate.

(2S,3S,4S)-3,4-다이하이드록시글루타믹산의 효율적인 입체선택적 합성 (Efficient Stereoselective Synthesis of (2S,3S,4S)-3,4-Dihydroxyglutamic Acid)

  • 전종호;신나라;이종협;김영규
    • 공업화학
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    • 제25권4호
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    • pp.392-395
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    • 2014
  • 생리학적 활성을 가진 (2S,3S,4S)-3,4-다이하이드록시 글루타믹산(DHGA)을 값이 저렴하고 수급이 용이한 D-serine 유도체로부터 효율적으로 합성하였다. D-serine 유도체로부터 얻어진 ${\gamma}$-아미노-${\alpha},{\beta}$-불포화성(Z)-에스터의 아민에 다이페닐메틸렌기를 도입, 이를 이용한 입체선택적 이 중 알코올화 반응을 통해 2,3 위치에 두 개의 하이드록시기를 10 : 1 이상의 높은 선택성과 86%의 높은 수율로 도입하여 중간체 5a를 효율적으로 합성하였고, 이 중간체의 간단한 산화 및 가수분해 반응을 통해 (2S,3S,4S)-3,4-DHGA 합성에 성공하였다. 이는 11단계에 총 30%의 수율과 입체선택적인 결과로 현재까지 보고된 (2S,3S,4S)-3,4-DHGA의 합성법 중에 가장 효율적이다. 이 결과는 $OsO_4$을 이용한 입체선택적 이중 알콜화 반응이 아미노 다이올을 포함하는 다양한 생리활성 물질의 효율적인 합성에 적용할 수 있음을 뒷받침한다.