Nowa wersja platformy, zawierająca wyłącznie zasoby pełnotekstowe, jest już dostępna.
Przejdź na https://bibliotekanauki.pl

PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Czasopismo
2014 | 1 | 1 |
Tytuł artykułu

Biocatalytic deracemization: An efficient one-pot synthesis of (R)-α-methyl-4-pyridinemethanol using whole cells of Candida parapsilosis

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A single-step synthesis of (R)-α-methyl- 4-pyridinemethanol from (RS)-α-methyl-4- pyridinemethanol by stereoinversion using whole cells of Candida parapsilosis is reported. Among the various strains of Candida species examined, C. parapsilosis demonstrated to have the best oxidoreductase system for stereoinversion of (RS)-α-methyl-4-pyridinemethanol. The effect of various physicochemical parameters on the stereoinversion process, were studied. Under optimized conditions approximately 97% enantiomeric excess of (R)-α-methyl-4-pyridinemethanol (eeR) was obtained with 99% yield was obtained. The optimized parameters were determined to be a substrate concentration of 5 mM, pH 8.0, 30°C incubation temperature, and a reaction time of 48 h. The reactions were also carried out in different organic solvents, and maximum stereoinversion was obtained in 1,4-dioxane with 78.4% eeR and 74.7% yield, which are lower than those in phosphate buffer. This whole cell catalysis for the preparation of (R)-α-methyl-4- pyridinemethanol is an example of a green, enantiopure synthesis of secondary alcohols.
EN
Wydawca

Czasopismo
Rocznik
Tom
1
Numer
1
Opis fizyczny
Daty
otrzymano
2015-05-15
zaakceptowano
2015-07-20
online
2015-09-10
Twórcy
  • Department of Pharmaceutical
    Technology, National Institute of Pharmaceutical Education and
    Research, Sector-67, S. A. S. Nagar-160062, Punjab, India
autor
  • Department of Pharmaceutical
    Technology, National Institute of Pharmaceutical Education and
    Research, Sector-67, S. A. S. Nagar-160062, Punjab, India
  • Department of Pharmaceutical
    Technology, National Institute of Pharmaceutical Education and
    Research, Sector-67, S. A. S. Nagar-160062, Punjab, India
Bibliografia
  • [1] Uskokovic M.R., Lewis R.L., Partridge J.J., Despreaux C.W.,Pruess D.L., Asymmetric synthesis of allo-heteroyohimbinealkaloids, J. Am. Chem. Soc., 1979, 101, 6742-6744.[Crossref]
  • [2] Kaneoya M., Uchida M., Yoshida N., U.S. Patent No. 4,971,909,1990.
  • [3] Quallich G.J., Woodall T.M., Diphenyloxazaborolidine a newcatalyst for enantio-selective reduction of ketones, TetrahedronLett., 1993, 34, 4145-4148.[Crossref]
  • [4] Collomb P., Von Zelewsky A., Synthesis of new chiral catalysts,pyridyl-and bipyridyl-alcohols, for the enantioselectiveaddition of diethylzinc to benzaldehyde, Tetrahedron:Asymmetry, 1998, 9, 3911-3917.[Crossref]
  • [5] Okano K., Murata K., Ikariya T., Stereoselective synthesisof optically active pyridyl alcohols via asymmetric transferhydrogenation of pyridyl ketones, Tetrahedron Lett., 2000, 41,9277-9280.[Crossref]
  • [6] Brown E., Penfornis A., Bayma J., Touet J., Asymmetricreductions of ketones using lithium aluminium hydridemodified with N, N-dialkyl derivatives of (R)-(−)-2-aminobutan-1-ol, Tetrahedron: Asymmetry, 1991, 2, 339-342.[Crossref]
  • [7] Lee J.H., Kim N., Kim M.J., Park J., Substituent effect on catalyticactivities of [{η5- Ar4C4COC(=O)Ar}Ru(CO)2Cl] in racemizationand DKR of secondary alcohols, ChemCatChem, 2011, 3,354-359.
  • [8] Seemayer R., Schneider M.P., Preparation of optically purepyridyl-1-ethanols, Tetrahedron: Asymmetry, 1992, 3, 827-830.[Crossref]
  • [9] Uenishi J.I., Hiraoka T., Hata S., Nishiwaki K., Yonemitsu O.,Nakamura K., Tsukube H., Chiral pyridines: optical resolutionof 1-(2-pyridyl)-and 1-[6-(2, 2’-bipyridyl)] ethanols by lipasecatalyzedenantioselective acetylation, J. Org. Chem., 1998, 63,2481-2487.[Crossref]
  • [10] Hatzakis N.S., Smonou I., Asymmetric transesterificationof secondary alcohols catalyzed by feruloyl esterase fromHumicola insolens, Bioorg. Chem., 2005, 33, 325-337.[Crossref]
  • [11] Laumen K., Schneider M.P., A highly selective ester hydrolasefrom Pseudomonas sp. for the enzymatic preparation ofenantiomerically pure secondary alcohols; chiral auxiliaries inorganic synthesis, Chem Commun., 1988, 9, 598-600.[Crossref]
  • [12] Gruber C.C., Lavandera I., Faber K., Kroutil W., From a racemateto a single enantiomer: deracemization by stereoinversion,Adv. Synth. Catal., 2006, 348, 1789-1805.
  • [13] Voss C.V., Gruber C.C., Kroutil W., Deracemization of secondaryalcohols through a concurrent tandem biocatalytic oxidationand reduction, Angew. Chem., Int. Ed., 2008, 47, 741-745.[Crossref][WoS]
  • [14] Nie Y., Xu Y., Mu X.Q., Highly enantioselective conversion ofracemic 1-phenyl-1, 2-ethanediol by stereoinversion involvinga novel cofactor-dependent oxidoreduction system of Candidaparapsilosis CCTCC M203011, Org. Process Res. Dev., 2004, 8,246-251.[Crossref]
  • [15] Nakamura K., Fujii M., Ida Y., Stereoinversion of arylethanolsby Geotrichum candidum, Tetrahedron: Asymmetry, 2001, 12,3147-3153.[Crossref]
  • [16] Xie S.X., Ogawa J., Shimizu S., Production of (R)-3-pentyn-2-olthrough stereoinversion of racemic 3-pentyn-2-ol by Nocardiafusca AKU 2123. Appl. Microbiol. Biotechnol. 1999, 52, 327-331.[Crossref]
  • [17] Gamenara D., Domínguez de María P., Candida spp. redoxmachineries: An ample biocatalytic platform for practicalapplications and academic insights. Biotechnol. Adv., 2009,27, 278-285.[WoS][Crossref]
  • [18] Nestl B.M., Voss C.V., Bodlenner A., Ellmer-Schaumberger U.,Kroutil W., Faber K., Biocatalytic racemization of sec-alcoholsand α-hydroxyketones using lyophilized microbial cells, Appl.Microbiol. Biotechnol., 2007, 76, 1001-1008.[Crossref][WoS]
  • [19] Baskar B., Pandian N.G., Priya K., Chadha A., Deracemisationof aryl substituted α-hydroxy esters using Candida parapsilosisATCC 7330: effect of substrate structure and mechanism,Tetrahedron, 2005, 61, 12296-12306.
  • [20] Banoth L., Banerjee U.C., New Chemical and Chemo-enzymaticsynthesis of (RS)-, (R)-, and (S)-Esmolol, Arabian J. Chem., (inpress), DOI:10.1016/j.arabjc.2014.03.011.[Crossref]
  • [21] Padhi S.K., Chadha A., Deracemisation of aromatic β-hydroxyesters using immobilized whole cells of Candida parapsilosisATCC 7330 and determination of absolute configuration by 1HNMR, Tetrahedron: Asymmetry, 2005, 16, 2790-2798.
  • [22] Titu D., Chadha A., Enantiomerically pure allylic alcohols:preparation by Candida parapsilosis ATCC 7330 mediatedderacemisation, Tetrahedron: Asymmetry, 2008, 19, 1698-1701.[WoS][Crossref]
  • [23] Saravanan T., Chadha A., Biocatalytic deracemization ofalkyl-2-hydroxy-4-arylbut-3-ynoates using whole cells ofCandida parapsilosis ATCC 7330, Tetrahedron: Asymmetry,2010, 21, 2973-2980.[WoS][Crossref]
  • [24] Guezane S.L., Djerourou A., Esterification and etherificationof steroid and terpene under Mitsunobu conditions, Arabian J.Chem., (in press), DOI: 10.1016/j.arabjc.2011.09.008.[Crossref]
  • [25] Salihu A., Alam M.Z., Karim M.I.A., Salleh H.M., Esterificationfor butyl butyrate formation using Candida cylindracea lipaseproduced from palm oil mill effluent supplemented medium,Arabian J. Chem., (in press), DOI: 10.1016/j.arabjc.2013.08.012.[WoS][Crossref]
  • [26] Orrenius C., Mattson A., Norin T., Ohrner N., Hult K.,Preparation of 1-pyridinyl-ethanols of high enantiomericpurity by lipase catalysed transesterifications, Tetrahedron:Asymmetry, 1994, 5, 1363-1366.[Crossref]
  • [27] Soni P., Kaur G., Chakraborti A., Banerjee U.C., Candidaviswanathii as a novel biocatalyst for stereoselective reductionof heteroaryl methyl ketones: A highly efficient enantioselectivesynthesis of (S)-α-(3-pyridyl)ethanol. Tetrahedron:Asymmetry, 2005, 16, 2425-2428.[Crossref]
  • [28] Päiviö M., Mavrynsky D., Leino R., Kanerva, L.T., Dynamickinetic resolution of a wide range of secondary alcohols:Cooperation of dicarbonylchlorido(pentabenzylcyclopentadienyl)ruthenium and CAL-B, Eur. J. Org. Chem., 2011,1452-1457.[Crossref][WoS]
  • [29] Machado L.L., Gonzalo G.D., Lemos T.L.G., Mattosa M.C.D.,Oliveira, M.C.F., Fernández V.G., Gotor V., Enantioselectiveacetylation of racemic alcohols by Manihot esculenta andPassiflora edulis preparations, J. Mol. Catal. B: Enzymatic,2009, 60, 157-162.[WoS][Crossref]
  • [30] Singh A., Chisti Y., Banerjee U.C., Stereoselective biocatalytichydride transfer to substituted acetophenones by the yeastMetschnikowia koreensis, Process Biochem., 2012, 47,2398-2404.[Crossref][WoS]
  • [31] Kansal H., Banerjee U.C., Enhancing the biocatalytic potentialof carbonyl reductase of Candida viswanathii using aqueousorganicsolvent system. Bioresour. Technol., 2009, 100,1041-1047.[Crossref][WoS]
  • [32] Stella S., Chadha A., Biocatalytic reduction of α-keto amides to(R)-α-hydroxy amides using Candida parapsilosis ATCC 7330,Catal. Today, 2012, 198, 345-352.[WoS]
  • [33] Zhu D., Malik H.T., Hua L., Asymmetric ketone reduction bya hyperthermophilic alcohol dehydrogenase. The substratespecificity, enantioselectivity and tolerance of organic solvents,Tetrahedron: Asymmetry, 2006, 17, 3010-3014.[Crossref]
  • [34] Laane C., Boeren S., Vos K., Veeger C. Rules for optimization ofbiocatalysis in organic solvents, Biotechnol. Bioeng., 1987, 30,81-87.[Crossref]
  • [35] Nakamura K., Inoue Y., Ohno A., Improvement of enantioselectivityof microbial reduction by using organic solvent redoxcoupler system, Tetrahedron Lett., 1995, 36, 265-266[Crossref]
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_1515_boca-2015-0004
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.