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Volumn 19, Issue 6, 2008, Pages 672-681

Preliminary investigation of the yeast-mediated reduction of β-keto amides derived from cyclic amines as potential resolution methodology

Author keywords

[No Author keywords available]

Indexed keywords

1 (2 CYCLOHEXYLPIPERIDIN 1 YL) 3 HYDROXY BUTAN 1 ONE; 1 (2 CYCLOHEXYLPIPERIDIN 1 YL) BUTANE 1,3 DIONE; 1 (2 METHYLPIPERIDIN 1 YL) BUTANE 1,3 DIONE; 1 (2 PHENYL 3,4 DIHYDRO 2H QUINOLIN 1 YL) BUTANE 1,3 DIONE; 2 CYCLOHEXYLPIPERIDINE; 2 PIPECOLINE; 3 HYDROXY 1 (2 METHYLPIPERIDIN 1 YL) BUTAN 1 ONE; 3 HYDROXY 1 (2 PHENYL 3,4 DIHYDRO 2H QUINOLIN 1 YL) BUTAN 1 ONE; AMIDE; AMINE; BETA KETO AMIDE DERIVATIVE; KETENE DERIVATIVE; PIPERIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 41449085881     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.02.021     Document Type: Article
Times cited : (7)

References (43)
  • 29
    • 41449087642 scopus 로고    scopus 로고
    • The surprising absence of such investigations until 1991 was most likely due to the lack of yeast reductions of esters other than those derived from methyl, ethyl, propyl, butyl and benzyl alcohols, the most commonly used substrates.
    • The surprising absence of such investigations until 1991 was most likely due to the lack of yeast reductions of esters other than those derived from methyl, ethyl, propyl, butyl and benzyl alcohols, the most commonly used substrates.
  • 31
    • 41449110218 scopus 로고    scopus 로고
    • Hudlicky, T.; Seoane, G.; Price, J. D.; Gadamasetti, K. (in part) Synlett 1990, 433.
    • Hudlicky, T.; Seoane, G.; Price, J. D.; Gadamasetti, K. (in part) Synlett 1990, 433.
  • 38
    • 41449086316 scopus 로고    scopus 로고
    • We want to thank Núria Llor and Professor Joan Bosch for helpful advice for the synthesis of the enantiomerically enriched standard 26. In repetition of this work, we were unable to obtain the enantiomeric excess of 99% reported (Ref. 13).
    • We want to thank Núria Llor and Professor Joan Bosch for helpful advice for the synthesis of the enantiomerically enriched standard 26. In repetition of this work, we were unable to obtain the enantiomeric excess of 99% reported (Ref. 13).
  • 39
    • 41449098366 scopus 로고    scopus 로고
    • No resolution with yeast reduction was observed for 2-phenyl-3,4-dihydro-2H-quinoline as substrate{A figure is presented}.
    • No resolution with yeast reduction was observed for 2-phenyl-3,4-dihydro-2H-quinoline as substrate{A figure is presented}.
  • 40
    • 41449110592 scopus 로고    scopus 로고
    • K1 V1116, EC 1118, CY 3079, and BA 11 are commercial wine yeast strains available from Scott Laboratories.
    • K1 V1116, EC 1118, CY 3079, and BA 11 are commercial wine yeast strains available from Scott Laboratories.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.