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Volumn 11, Issue 21, 2009, Pages 4994-4997

Highly enantioselective synthesis of chiral cyclic amino alcohols and conhydrine by ruthenium-catalyzed asymmetric hydrogenation

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; ALPHA-CONHYDRINE; AMINOALCOHOL; CONHYDRINE; PIPERIDINE DERIVATIVE; RUTHENIUM;

EID: 70350635784     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol901605a     Document Type: Article
Times cited : (50)

References (37)
  • 6
    • 0038384650 scopus 로고    scopus 로고
    • For recent examples of asymmetric hydrogénation of racemic a-substituted cycloketones, see: (a) Scalone, M.; Waldmeier, P. Org. Process Res. Dev. 2003, 7, 418.
    • (2003) Org. Process Res. Dev. , vol.7 , pp. 418
    • Scalone, M.1    Waldmeier, P.2
  • 16
    • 0034641294 scopus 로고    scopus 로고
    • 2((S)-Xyl-BINAP)(R)- DaiPEN]-catalyzed asymmetric hydrogenation of racemic a-amino cyclohexanone, but the amino group was protected by tert-butoxycarbonyl; see: (c) Ohkuma, T.; Ishii, D.; Takeno, H.; Noyori, R. J. Am. Chem. Soc. 2000, 122, 6510.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 6510
    • Ohkuma, T.1    Ishii, D.2    Takeno, H.3    Noyori, R.4
  • 37
    • 70350638498 scopus 로고    scopus 로고
    • 2 group of the chiral diamine in the catalyst. See ref 3e
    • 2 group of the chiral diamine in the catalyst. See ref 3e.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.