메뉴 건너뛰기




Volumn 68, Issue 1, 1997, Pages 57-64

Enzymatic transesterification of 3,7-dimethyl-4,7-octadien-1-ol using lipases

Author keywords

(R) 3,7 dimethyl 4,7 octadien 1 ol; Lipases; Rose oxide; Transesterification

Indexed keywords

ALCOHOLS; ESTERIFICATION; ESTERS; SYNTHESIS (CHEMICAL);

EID: 0031017555     PISSN: 02682575     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-4660(199701)68:1<57::AID-JCTB607>3.0.CO;2-A     Document Type: Article
Times cited : (9)

References (17)
  • 1
    • 84984085179 scopus 로고
    • Zur Kenntnis des Rosenöls 1. Mitteilung. Uber die tiefseidenden Bestandteile des bulgarischen Rosenöls
    • Seidel, C. F. & Stoll, M., Zur Kenntnis des Rosenöls 1. Mitteilung. Uber die tiefseidenden Bestandteile des bulgarischen Rosenöls. Helv. Chim. Acta, 42 (1959) 1830-44.
    • (1959) Helv. Chim. Acta , vol.42 , pp. 1830-1844
    • Seidel, C.F.1    Stoll, M.2
  • 2
    • 0002810255 scopus 로고
    • Études sur les matieres végétales volatiles CLXXIV (1). Présence de tétrahydropyrannes dans l'huile essentielle de géranium
    • Naves, Y.-R., Lamparsky, D. & Ochsner, P., Études sur les matieres végétales volatiles CLXXIV (1). Présence de tétrahydropyrannes dans l'huile essentielle de géranium. Bull. Soc. Chim. Fr., (1961) 645-7.
    • (1961) Bull. Soc. Chim. Fr. , pp. 645-647
    • Naves, Y.-R.1    Lamparsky, D.2    Ochsner, P.3
  • 3
    • 0000267883 scopus 로고
    • Darstellung von 'Rosenoxyden' und anderen Hydropyran-Derivaten über Photohydroperoxyde
    • Ohloff, G., Klein, E. & Schenck, G. O., Darstellung von 'Rosenoxyden' und anderen Hydropyran-Derivaten über Photohydroperoxyde. Angew. Chem., 73 (1961) 578.
    • (1961) Angew. Chem. , vol.73 , pp. 578
    • Ohloff, G.1    Klein, E.2    Schenck, G.O.3
  • 4
    • 0000666267 scopus 로고
    • A new synthesis of rosoxides. Cis and trans-2-(2-methyl-1-propen-1-yl)-4-methyltetrahydropyran
    • Eschinasi, E. H., A new synthesis of rosoxides. Cis and trans-2-(2-methyl-1-propen-1-yl)-4-methyltetrahydropyran. J. Org. Chem., 35 (1970) 1097-100.
    • (1970) J. Org. Chem. , vol.35 , pp. 1097-1100
    • Eschinasi, E.H.1
  • 5
    • 0000296312 scopus 로고
    • A novel synthesis of DL-marmelolactone and DL-rose oxide by electrochemical oxyselenylation-deselenylation sequence
    • Torii, S., Uneyama, K. & Ono, M., A novel synthesis of DL-marmelolactone and DL-rose oxide by electrochemical oxyselenylation-deselenylation sequence. Tetrahedron Lett., 21 (1980) 2653-4.
    • (1980) Tetrahedron Lett. , vol.21 , pp. 2653-2654
    • Torii, S.1    Uneyama, K.2    Ono, M.3
  • 6
    • 2642665727 scopus 로고
    • A rose oxide synthesis
    • Ho, T.-L. & Din, Z. U., A rose oxide synthesis. Synth. Commun., 12 (1982) 1099-102.
    • (1982) Synth. Commun. , vol.12 , pp. 1099-1102
    • Ho, T.-L.1    Din, Z.U.2
  • 7
    • 0000948833 scopus 로고
    • 4 induced cyclization of acetals: Application to a synthesis of rose oxide
    • 4 induced cyclization of acetals: application to a synthesis of rose oxide. Tetrahedron Lett., 30 (1989) 1971-4.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 1971-1974
    • Wagner, A.1    Heitz, M.-P.2    Mioskowski, C.3
  • 8
    • 84956922070 scopus 로고
    • Etudes sur les matieres végétales volatiles CLXXIX. Syntheses des cis et trans-[méthyl-2-propene-1]-yl-2-méthyl-4-tétrahydropyrans
    • Naves, Y.-R. & Tullen, P., Etudes sur les matieres végétales volatiles CLXXIX. Syntheses des cis et trans-[méthyl-2-propene-1]-yl-2-méthyl-4-tétrahydropyrans. Helv. Chim. Acta, 44 (1961) 1861-72.
    • (1961) Helv. Chim. Acta , vol.44 , pp. 1861-1872
    • Naves, Y.-R.1    Tullen, P.2
  • 9
    • 0542414716 scopus 로고
    • N-Iodosuccinimide for the synthesis of rose oxide
    • Taneja, S. C., Dhar, K. L. & Atal, C. K., N-Iodosuccinimide for the synthesis of rose oxide. J. Org. Chem., 43 (1978) 997-8.
    • (1978) J. Org. Chem. , vol.43 , pp. 997-998
    • Taneja, S.C.1    Dhar, K.L.2    Atal, C.K.3
  • 10
    • 0001917711 scopus 로고
    • Electrooxidative cleavage of carbon - Carbon linkage. 1. Preparation of acyclic oxoalkanoates from 2-hydroxy- and 2-acetoxy-1-cycloalkanones and cycloalkanones enol acetates
    • Torii, S., Inokuchi, T. & Oi, R., Electrooxidative cleavage of carbon - carbon linkage. 1. Preparation of acyclic oxoalkanoates from 2-hydroxy- and 2-acetoxy-1-cycloalkanones and cycloalkanones enol acetates. J. Org. Chem., 47 (1982) 47-52.
    • (1982) J. Org. Chem. , vol.47 , pp. 47-52
    • Torii, S.1    Inokuchi, T.2    Oi, R.3
  • 11
    • 0000324866 scopus 로고
    • Stereoselective syntheses of α-substituted cyclic ethers and syn-1, 3-diols
    • Homma, K., Takenoshita, H. & Mukaiyama, T., Stereoselective syntheses of α-substituted cyclic ethers and syn-1, 3-diols. Bull. Chem. Soc. Jpn., 63 (1990) 1898-915.
    • (1990) Bull. Chem. Soc. Jpn. , vol.63 , pp. 1898-1915
    • Homma, K.1    Takenoshita, H.2    Mukaiyama, T.3
  • 12
    • 0026671559 scopus 로고
    • On the mode of baker's yeast reduction of methyl substituted arylalkyl gamma and delta keto acids. Synthesis of cis-(+)-rose oxide
    • Fronza, G., Tuganti, C., Grasselli, P. & Terreni, M., On the mode of baker's yeast reduction of methyl substituted arylalkyl gamma and delta keto acids. Synthesis of cis-(+)-rose oxide. Tetrahedron, 48 (1992) 7363-72.
    • (1992) Tetrahedron , vol.48 , pp. 7363-7372
    • Fronza, G.1    Tuganti, C.2    Grasselli, P.3    Terreni, M.4
  • 13
    • 15644366400 scopus 로고
    • Vinyl esters by transscylation. Ger. Offen. 2,214,627
    • Plettner, W., Vinyl esters by transscylation. Ger. Offen. 2,214,627: Chem. Abstr., 79 (1973) 146012h.
    • (1973) Chem. Abstr. , vol.79
    • Plettner, W.1
  • 14
    • 33845279035 scopus 로고
    • Lipase-catalyzed irreversible transesterifications using enol esters as acylating reagents; preparative enantio- and regioselective synthesis of alcohols, glycerol derivatives, sugars and organometallics
    • Wang, Y.-F., Lalonde, J. J., Mamongan, M., Bergbreitere, D. E. & Wong, C.-H., Lipase-catalyzed irreversible transesterifications using enol esters as acylating reagents; preparative enantio- and regioselective synthesis of alcohols, glycerol derivatives, sugars and organometallics. J. Am. Chem. Soc., 110 (1988) 7200-5.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 7200-7205
    • Wang, Y.-F.1    Lalonde, J.J.2    Mamongan, M.3    Bergbreitere, D.E.4    Wong, C.-H.5
  • 15
    • 0040537914 scopus 로고
    • Enzymatic kinetic resolution of [4] (1,2)ferrocenophane derivatives
    • Izumi, T., Tamura, F. & Sasaki, K., Enzymatic kinetic resolution of [4] (1,2)ferrocenophane derivatives. Bull. Chem. Soc. Jpn, 65 (1992) 2784-8.
    • (1992) Bull. Chem. Soc. Jpn , vol.65 , pp. 2784-2788
    • Izumi, T.1    Tamura, F.2    Sasaki, K.3
  • 16
    • 0001364513 scopus 로고
    • Enantioselective esterification of unsaturated alcohols mediated by a lipase from Pseudomonas sp
    • Burgess, K. & Jennings, L. D., Enantioselective esterification of unsaturated alcohols mediated by a lipase from Pseudomonas sp. J. Am. Chem. Soc., 113 (1991) 6129-39.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 6129-6139
    • Burgess, K.1    Jennings, L.D.2
  • 17
    • 0242528545 scopus 로고
    • Enantiopreference lipase from Pseudomonas cepacia toward primary alcohols
    • Weissfloch, A. N. E. & Kazlauskas, R. J., Enantiopreference lipase from Pseudomonas cepacia toward primary alcohols. J. Org. Chem., 60 (1995) 6959-69.
    • (1995) J. Org. Chem. , vol.60 , pp. 6959-6969
    • Weissfloch, A.N.E.1    Kazlauskas, R.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.