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Volumn 62, Issue 23, 2006, Pages 5448-5453

Mechanism of catalytic asymmetric hydrogenation of 2-formyl-1-methylene-1,2,3,4-tetrahydroisoquinoline using Ru(CH3COO)2[(S)-binap]

Author keywords

2 Acyl 1 alkylidene 1,2,3,4 tetrahydroisoquinoline; Asymmetric hydrogenation; BINAP Ru; Monohydride unsaturated mechanism

Indexed keywords

2 ACYL 1 ALKYLIDENE 1,2,3,4 TETRAHYDROISOQUINOLINE; ALKENE; ISOQUINOLINE DERIVATIVE; RUTHENIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33646197286     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.03.055     Document Type: Article
Times cited : (8)

References (39)
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    • Reviews:
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    • N-Acetyl phenylalanine in >80% enantiomeric excess (ee) was obtained by the use of a DIOP-Rh(I) complex (DIOP=2,3-O-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane)
    • Dang T.P., and Kagan H.B. J. Chem. Soc., Chem. Commun. (1971) 481-482 N-Acetyl phenylalanine in >80% enantiomeric excess (ee) was obtained by the use of a DIOP-Rh(I) complex (DIOP=2,3-O-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane)
    • (1971) J. Chem. Soc., Chem. Commun. , pp. 481-482
    • Dang, T.P.1    Kagan, H.B.2
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    • For recent advancement in the chiral Rh complex-catalyzed asymmetric hydrogenation, see:
  • 12
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    • Jacobsen E., Pfaltz A., and Yamamoto H. (Eds), Springer, Berlin Chapter 5.1
    • Brown M. In: Jacobsen E., Pfaltz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Catalysis Vol. I (1999), Springer, Berlin Chapter 5.1
    • (1999) Comprehensive Asymmetric Catalysis , vol.I
    • Brown, M.1
  • 16
    • 33646193637 scopus 로고    scopus 로고
    • For hydrogenation using a cationic BINAP-Ru complex, see:
  • 22
    • 0030004127 scopus 로고    scopus 로고
    • For the conformational study on 2-acyl-1-alkylidene-1,2,3,4-tetrahydroisoquinolines, see:
    • For the conformational study on 2-acyl-1-alkylidene-1,2,3,4-tetrahydroisoquinolines, see:. Kitamura M., Tsukamoto M., Takaya H., and Noyori R. Bull. Chem. Soc. Jpn. 69 (1996) 1695-1700
    • (1996) Bull. Chem. Soc. Jpn. , vol.69 , pp. 1695-1700
    • Kitamura, M.1    Tsukamoto, M.2    Takaya, H.3    Noyori, R.4
  • 28
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    • For Ru dihydride mechanism proposed for ketone hydrogenation with BINAP-Ru complexes, see:
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    • note
    • The constant 'a' (0
  • 33
    • 33646205176 scopus 로고    scopus 로고
    • Discussion on the origin of the minor enantiomer in BINAP-Ru catalyzed asymmetric hydrogenation:
  • 39
    • 33845278799 scopus 로고
    • For the first report on the preparation of BINAP-Ru dicarboxylate complexes, see:
    • For the first report on the preparation of BINAP-Ru dicarboxylate complexes, see:. Ohta T., Takaya H., and Noyori R. Inorg. Chem. 27 (1988) 566-569
    • (1988) Inorg. Chem. , vol.27 , pp. 566-569
    • Ohta, T.1    Takaya, H.2    Noyori, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.