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Volumn 129, Issue 7, 2007, Pages 1868-1869

Ru-catalyzed asymmetric hydrogenation of racemic aldehydes via dynamic kinetic resolution: Efficient synthesis of optically active primary alcohols

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; ALDEHYDE DERIVATIVE; DIAMINE DERIVATIVE; KETONE; PHOSPHINE DERIVATIVE; RUTHENIUM;

EID: 33847307475     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0680109     Document Type: Article
Times cited : (88)

References (31)
  • 1
    • 0003445429 scopus 로고    scopus 로고
    • Jacobsen, E. N, Pfaltz, A, Yamamoto, H, Eds, Springer: Berlin, Vols
    • (a) Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds. In Comprehensive Asymmetric Catalysis; Springer: Berlin, 1999; Vols. 1-3.
    • (1999) Comprehensive Asymmetric Catalysis , vol.1-3
  • 14
    • 0043240879 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Tang, W.-J.; Zhang, X.-M. Chem. Rev. 2003, 103, 3029.
    • (2003) Chem. Rev , vol.103 , pp. 3029
    • Tang, W.-J.1    Zhang, X.-M.2
  • 19
    • 0006274499 scopus 로고    scopus 로고
    • By this definition, the deuterated benzaldehyde (PhCDO) can be regarded as a ketone. For asymmetric hydrogenation of 1-deuteriobenzaldehyde, see: (a) Ohta, T.; Tsutsumi, T.; Takaya, H. J. Organomet. Chem. 1994, 484, 191.
    • By this definition, the deuterated benzaldehyde (PhCDO) can be regarded as a ketone. For asymmetric hydrogenation of 1-deuteriobenzaldehyde, see: (a) Ohta, T.; Tsutsumi, T.; Takaya, H. J. Organomet. Chem. 1994, 484, 191.
  • 21
    • 1442358656 scopus 로고    scopus 로고
    • Hydrogen-transfer reduction of α-branched aldehydes has been reported, but asymmetric version of this reaction has not been documented. (a) Miecznikowski, J. R.; Crabtree, R.H. Organometallics 2004, 23, 629.
    • Hydrogen-transfer reduction of α-branched aldehydes has been reported, but asymmetric version of this reaction has not been documented. (a) Miecznikowski, J. R.; Crabtree, R.H. Organometallics 2004, 23, 629.
  • 31
    • 0037067066 scopus 로고    scopus 로고
    • 4)((R)-BINAP)((R,R)-DPEN)] were prepared and used to catalyze the hydrogenation of 1c under base-free conditions. Both catalysts gave <5% ee of enantioselectivity at 40% conversion. Ohkuma, T.; Koizumi, M.; Muñiz, K.; Hilt, G.; Kabuto, C.; Noyori, R. J. Am. Chem. Soc. 2002, 124, 6508.
    • 4)((R)-BINAP)((R,R)-DPEN)] were prepared and used to catalyze the hydrogenation of 1c under base-free conditions. Both catalysts gave <5% ee of enantioselectivity at 40% conversion. Ohkuma, T.; Koizumi, M.; Muñiz, K.; Hilt, G.; Kabuto, C.; Noyori, R. J. Am. Chem. Soc. 2002, 124, 6508.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.