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Volumn 38, Issue 29, 1997, Pages 5193-5196

Stereodivergent approach to syn- and anti 2-amino-1,2-diarylethanols using oxazaborolidine-mediated asymmetric reduction

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINO 1,2 DIARYLETHANOL; AMINOALCOHOL; UNCLASSIFIED DRUG;

EID: 0030803347     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)01125-8     Document Type: Article
Times cited : (34)

References (26)
  • 19
    • 0342372840 scopus 로고    scopus 로고
    • The starting materials, 1,2-diaryl-2-benzyloxyiminoethanones 2c-g, were prepared readily from monoimination of benzil derivatives in yields ranging from 46-99%
    • The starting materials, 1,2-diaryl-2-benzyloxyiminoethanones 2c-g, were prepared readily from monoimination of benzil derivatives in yields ranging from 46-99%.
  • 20
    • 0343242415 scopus 로고    scopus 로고
    • note
    • 14 which was benzyloxyiminated to afford 4g and compared using HPLC.
  • 23
    • 0343678001 scopus 로고    scopus 로고
    • note
    • 14,15 3f was transformed into 3c (R = H) by reduction with n-BuLi, and analyzed by its specific rotation.
  • 26
    • 0029937757 scopus 로고    scopus 로고
    • and the references cited therein
    • Chang, H.-T.; Sharpless, K. B. Tetrahedron Lett. 1996, 37, 3219-3222, and the references cited therein.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3219-3222
    • Chang, H.-T.1    Sharpless, K.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.