메뉴 건너뛰기




Volumn 16, Issue 9, 2011, Pages 8098-8109

Enzymatic kinetic resolution of tert-butyl 2-(1-Hydroxyethyl) phenylcarbamate, a key intermediate to chiral organoselenanes and organotelluranes

Author keywords

Alcohols; Carbamates; Enatiopure; Kinetic resolution; Lipases

Indexed keywords

CARBAMIC ACID DERIVATIVE; FUNGAL PROTEIN; LIPASE B, CANDIDA ANTARCTICA; ORGANOMETALLIC COMPOUND; ORGANOSELENIUM DERIVATIVE; SOLVENT; TELLURIUM; TERT BUTYL 2 (1 HYDROXYETHYL)PHENYLCARBAMATE; TERT-BUTYL 2-(1-HYDROXYETHYL)PHENYLCARBAMATE; TRIACYLGLYCEROL LIPASE;

EID: 80053278034     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules16098098     Document Type: Article
Times cited : (3)

References (19)
  • 1
    • 0035385139 scopus 로고    scopus 로고
    • Chemistry of biologically important synthetic organoselenium compounds
    • DOI 10.1021/cr000426w
    • Mugesh, G.; du Mont, W.-W.; Sies, H. Chemistry of biologically important synthetic organoselenium compounds. Chem. Rev. 2001, 101, 2125-2179. (Pubitemid 35381674)
    • (2001) Chemical Reviews , vol.101 , Issue.7 , pp. 2125-2179
    • Mugesh, G.1    Du Mont, W.-W.2    Sies, H.3
  • 2
    • 77956482026 scopus 로고    scopus 로고
    • An element with great biological potency and potential
    • Ba, L.A.; Döring, M.; Jamier, V.; Jacob, C. Tellurium: An element with great biological potency and potential. Org. Biomol. Chem. 2010, 8, 4203-4216.
    • (2010) Org. Biomol. Chem. , vol.8 , pp. 4203-4216
    • Ba, L.A.1    Döring, M.2    Jamier, V.3    Tellurium, J.C.4
  • 3
    • 78649287952 scopus 로고    scopus 로고
    • Functional mimics of glutathione peroxidase bioinspired synthetic antioxidants
    • Brabak, K.P.; Mugesh, G. Functional mimics of glutathione peroxidase bioinspired synthetic antioxidants. Acc. Chem. Res. 2010, 43, 1408-1419.
    • (2010) Acc. Chem. Res. , vol.43 , pp. 1408-1419
    • Brabak, K.P.1    Mugesh, G.2
  • 4
    • 78649533121 scopus 로고    scopus 로고
    • Catalytic application of selenium and tellurium compounds as glutathione peroxidase enzyme mimetics
    • Alberto, E.E.; do Nascimento, V.; Braga, A.L. Catalytic application of selenium and tellurium compounds as glutathione peroxidase enzyme mimetics. J. Braz. Chem. Soc. 2010, 21, 2032-2041.
    • (2010) J. Braz. Chem. Soc. , vol.21 , pp. 2032-2041
    • Alberto, E.E.1    Do Nascimento, V.2    Braga, A.L.3
  • 5
    • 79952449578 scopus 로고    scopus 로고
    • Structure-activity relationships of hypervalent organochalcogenanes as inhibitors of cysteine cathepsins v and S
    • Piovan, L.; Alves, M.F.M.; Juliano, L.; Bromme, D.; Cunha, R.L.O.R.; Andrade, L.H. Structure-activity relationships of hypervalent organochalcogenanes as inhibitors of cysteine cathepsins V and S. Bioorg. Med. Chem. 2011, 19, 2009-2014.
    • (2011) Bioorg. Med. Chem. , vol.19 , pp. 2009-2014
    • Piovan, L.1    Alves, M.F.M.2    Juliano, L.3    Bromme, D.4    Cunha, R.L.O.R.5    Andrade, L.H.6
  • 6
    • 78649587764 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of organoselenanium(IV) compounds and their evaluation as cysteine proteases inhibitors
    • Piovan, L.; Alves, M.F.M.; Juliano, L.; Bromme, D.; Cunha, R.L.O.R.; Andrade, L.H. Chemoenzymatic synthesis of organoselenanium(IV) compounds and their evaluation as cysteine proteases inhibitors. J. Braz. Chem. Soc. 2010, 21, 2108-2118.
    • (2010) J. Braz. Chem. Soc. , vol.21 , pp. 2108-2118
    • Piovan, L.1    Alves, M.F.M.2    Juliano, L.3    Bromme, D.4    Cunha, R.L.O.R.5    Andrade, L.H.6
  • 9
    • 79951627298 scopus 로고    scopus 로고
    • Hypervalent organochalcogenanes as inhibitors of protein tyrosine phosphatases
    • Piovan, L.; Wu, L.; Zhang, Z.Y.; Andrade, L.H. Hypervalent organochalcogenanes as inhibitors of protein tyrosine phosphatases. Org. Biomol. Chem. 2011, 9, 1347-1351.
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 1347-1351
    • Piovan, L.1    Wu, L.2    Zhang, Z.Y.3    Andrade, L.H.4
  • 11
    • 44449099152 scopus 로고    scopus 로고
    • First chemoenzymatic synthesis of organoselenium amines and amides
    • DOI 10.1016/j.tetasy.2008.04.026, PII S0957416608002838
    • Silva, A.; Andrade, L.H. First chemoenzymatic synthesis of organoselenium amines and amides. Tetrahedron: Asymmetry 2008, 19, 1175-1181. (Pubitemid 351758809)
    • (2008) Tetrahedron Asymmetry , vol.19 , Issue.10 , pp. 1175-1181
    • Andrade, L.H.1    Silva, A.V.2
  • 12
    • 34250007689 scopus 로고    scopus 로고
    • Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435
    • DOI 10.1016/j.tetasy.2007.04.019, PII S0957416607003072
    • Omori, A.T.; Assis, L.F.; Andrade, L.H.; Comasseto, J.V.; Porto, A.L.M. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435. Tetrahedron: Asymmetry 2007, 18, 1048-1053. (Pubitemid 46881122)
    • (2007) Tetrahedron Asymmetry , vol.18 , Issue.9 , pp. 1048-1053
    • Omori, A.T.1    Assis, L.F.2    Andrade, L.H.3    Comasseto, J.V.4    Porto, A.L.M.5
  • 13
    • 0042698454 scopus 로고    scopus 로고
    • An efficient synthesis of ortho-N-Boc-arylmethyl ketone derivatives
    • DOI 10.1016/S0040-4039(03)01597-1
    • Broutin, P.-E.; Hilty, P.; Thomas, A.W. An efficient synthesis of ortho-N-Boc-arylmethyl ketone derivatives. Tetrahedron Lett. 2003, 44, 6429-6432. (Pubitemid 36936934)
    • (2003) Tetrahedron Letters , vol.44 , Issue.34 , pp. 6429-6432
    • Broutin, P.-E.1    Hilty, P.2    Thomas, A.W.3
  • 14
    • 0034803796 scopus 로고    scopus 로고
    • An improved synthesis of N-Boc protected aryl amines
    • DOI 10.1081/SCC-100106036
    • Darnbrough, S.; Mervic, M.; Condon, S.M.; Burns, C.J. An improved synthesis of N-Boc protected aryl amines. Syn. Commun. 2001, 31, 3273-3280. (Pubitemid 32912250)
    • (2001) Synthetic Communications , vol.31 , Issue.21 , pp. 3273-3280
    • Darnbrough, S.1    Mervic, M.2    Condon, S.M.3    Burns, C.J.4
  • 15
    • 33750025005 scopus 로고    scopus 로고
    • Molecular iodine-catalyzed facile procedure for N-Boc protection of amines
    • DOI 10.1021/jo0612473
    • Varala, R.; Nuvula, S.; Adapa, S.R. Molecular iodine-catalyzed facile procedure for N-Boc protection of amines. J. Org. Chem. 2006, 71, 8283-8286. (Pubitemid 44571844)
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.21 , pp. 8283-8286
    • Varala, R.1    Nuvula, S.2    Adapa, S.R.3
  • 17
    • 11144348653 scopus 로고    scopus 로고
    • Zinc-acetic acid reductive cyclisation in a two-step synthesis of the S1-N10 nine-membered lactone core of ent-griseoviridin
    • DOI 10.1055/s-2004-834899, Nickel in Organic Synthesis
    • Chaume, G.; Kuligowski, C.; Benzzenine-Laffolée, S.; Ricard, L.; Pancrazi, A.; Ardisson, J. Zinc-acetic acid reductive cyclisation in a two-step synthesis of the S1-N10 nine-membered lactone core of ent-griseoviridin. Synthesis 2004, 18, 3029-3036. (Pubitemid 40040352)
    • (2004) Synthesis , Issue.18 , pp. 3029-3036
    • Chaume, G.1    Kuligowski, C.2    Bezzenine-Laffolee, S.3    Ricard, L.4    Pancrazi, A.5    Ardisson, J.6
  • 18
    • 63249122358 scopus 로고    scopus 로고
    • An enantiopure galactose oxidase model: Synthesis of chiral amino alcohols through oxidative kinetic resolution catalyzed by a chiral copper complex
    • Mannan, S.; Sekar, G. An enantiopure galactose oxidase model: Synthesis of chiral amino alcohols through oxidative kinetic resolution catalyzed by a chiral copper complex. Tetrahedron: Asymmetry 2009, 20, 497-502.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 497-502
    • Mannan, S.1    Sekar, G.2
  • 19
    • 0000712103 scopus 로고
    • General procedure for the synthesis of mono-N-acylated 1,6-diaminohexanes
    • Stahl, G.L.; Walter, R.; Smith, C.W. General procedure for the synthesis of mono-N-acylated 1,6-diaminohexanes. J. Org. Chem. 1978, 43, 2285-2286
    • (1978) J. Org. Chem. , vol.43 , pp. 2285-2286
    • Stahl, G.L.1    Walter, R.2    Smith, C.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.