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Volumn , Issue 9, 1998, Pages 1352-1356

A general chemoenzymatic synthesis of enenatiopures cis β-amino alcohols from microbially derived cis-glycols

Author keywords

Absolute configurational assignments; Chemoenzymatic synthesis; cis amino alcohols; cis diols; Diastereomeric oxazaborolidines

Indexed keywords

AMINOALCOHOL;

EID: 0031656449     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-6082     Document Type: Article
Times cited : (12)

References (43)
  • 31
    • 34548198971 scopus 로고    scopus 로고
    • note
    • Induced cells of strain PpF39/D (300 mL) incubated for 24 h with 300 mg 2-indanol yielded 217 mg of crude products. Radial dispersion chromatography was used to isolate (-)-(1S,2R)-1,2-dihydroxyindane [(-)-1, 92% ee, 110 mg, >85% relative product yield], trans-1,2-dihydroxyindane (13 mg), and 2-hydroxyindan-1-one (<2 mg). The enantiomeric purity of (-)-1 was determined by chiral stationary phase HPLC.
  • 38
  • 43
    • 0000716076 scopus 로고    scopus 로고
    • Since submission of this manuscript other authors have reported difficulties in derivatizing propranolol, a β-amino alcohol, with phenylboronic acid: Hori, M.; Janda, K. D. J. Org. Chem. 1998, 63, 889.
    • (1998) J. Org. Chem. , vol.63 , pp. 889
    • Hori, M.1    Janda, K.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.