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Volumn 10, Issue 10, 1999, Pages 1843-1846

A practical method for synthesis of terminal 1,2-diols in high enantiomeric excess via oxazaborolidine-catalyzed asymmetric reduction

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUND; BORANE DERIVATIVE; GLYCOL; PYRAN DERIVATIVE;

EID: 0000321156     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(99)00184-6     Document Type: Article
Times cited : (36)

References (23)
  • 18
    • 0344481615 scopus 로고    scopus 로고
    • note
    • We also examined the same reduction of 2 protected with MOM, BOM, 1-ethoxyethyl (EE) and trimethylacetyl (Piv) groups using N,N-diethylaniline-borane. The reductions produced 5a with somewhat lower enantioselectivity (93-95% ee) than that for 3a protected with a THP group. The same catalytic asymmetric borane reduction for an unprotected α-hydroxy ketone 2a provided 5a in only 9% ee.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.