메뉴 건너뛰기




Volumn 27, Issue 16, 2005, Pages 1189-1193

Newly detected specific hydrogenation of the conjugated double bond of unsaturated alkaloid lactones by Aspergillus sp.

Author keywords

Aspergillus; Conjugated double bond reduction; Guaiatriene lactone; Lactones; Securinine

Indexed keywords

BONDING; CARBOXYLIC ACIDS; MICROORGANISMS; ORGANIC COMPOUNDS;

EID: 24744433718     PISSN: 01415492     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10529-005-0015-y     Document Type: Article
Times cited : (10)

References (11)
  • 1
    • 0021143099 scopus 로고
    • CMR assignments of the securinine alkaloids
    • JA Beutler P Livant 1984 CMR assignments of the securinine alkaloids J. Nat. Prod 47 677 681
    • (1984) J. Nat. Prod , vol.47 , pp. 677-681
    • Beutler, J.A.1    Livant, P.2
  • 3
    • 5344237369 scopus 로고    scopus 로고
    • Stereochemical aspects of the bioreduction of the conjugated double bond of perillaldehyde
    • G Fronza C Fuganti M Pinciroli S Serra 2004 Stereochemical aspects of the bioreduction of the conjugated double bond of perillaldehyde Tetrahedron: Asymmet 15 3073 3077
    • (2004) Tetrahedron: Asymmet , vol.15 , pp. 3073-3077
    • Fronza, G.1    Fuganti, C.2    Pinciroli, M.3    Serra, S.4
  • 4
    • 37049066460 scopus 로고
    • Stereochemistry of the baker's yeast mediated reduction of the C=C bond of (Z)- and (E)-5-ben zoyloxyhex-3-en-2-one
    • G Fronza C Fuganti P Grasselli S Lanati R Rallo S Tchilibon 1994 Stereochemistry of the baker's yeast mediated reduction of the C=C bond of (Z)- and (E)-5-ben zoyloxyhex-3-en-2-one J. Chem. Soc., Perkin Trans. 1 1 2927 2930
    • (1994) J. Chem. Soc., Perkin Trans. 1 , vol.1 , pp. 2927-2930
    • Fronza, G.1    Fuganti, C.2    Grasselli, P.3    Lanati, S.4    Rallo, R.5    Tchilibon, S.6
  • 5
    • 0034613331 scopus 로고    scopus 로고
    • Total syntheses of the Securinega alkaloids (+)-14,15- dihydronorsecurinine, (-)-norsecurinine, and phyllanthine
    • G Han MG Laporte JJ Folmer KM Werner SM Weinreb 2000 Total syntheses of the Securinega alkaloids (+)-14,15-dihydronorsecurinine, (-)-norsecurinine, and phyllanthine J. Org. Chem 65 6293 6306
    • (2000) J. Org. Chem , vol.65 , pp. 6293-6306
    • Han, G.1    Laporte, M.G.2    Folmer, J.J.3    Werner, K.M.4    Weinreb, S.M.5
  • 8
    • 0001127129 scopus 로고    scopus 로고
    • Stereochemical control in microbial reduction. X X VIII. Asymmetric reduction of α,β-unsaturated ketones with baker's yeast
    • Y Kawai K Saitou K Hida DH Dao A Ohno 1996 Stereochemical control in microbial reduction. X X VIII. Asymmetric reduction of α,β- unsaturated ketones with baker's yeast Bull. Chem. Soc. Jpn 69 2633 2638
    • (1996) Bull. Chem. Soc. Jpn , vol.69 , pp. 2633-2638
    • Kawai, Y.1    Saitou, K.2    Hida, K.3    Dao, D.H.4    Ohno, A.5
  • 10
    • 0347474982 scopus 로고    scopus 로고
    • Recent developments in asymmetric reduction of ketones with biocatalysts
    • K Nakamura R Yamanaka T Matsuda T Harada 2003 Recent developments in asymmetric reduction of ketones with biocatalysts Tetrahedron: Asymmet 14 2659 2681
    • (2003) Tetrahedron: Asymmet , vol.14 , pp. 2659-2681
    • Nakamura, K.1    Yamanaka, R.2    Matsuda, T.3    Harada, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.