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Volumn 692, Issue 14, 2007, Pages 3065-3069

An efficient catalytic system for the hydrogenation of quinolines

Author keywords

Hydrogenation; Iodine; Quinolines

Indexed keywords

CATALYST ACTIVITY; DERIVATIVES; HYDROGENATION; IODINE; REACTION KINETICS;

EID: 34249285496     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2007.03.032     Document Type: Article
Times cited : (38)

References (45)
  • 1
    • 29144521717 scopus 로고    scopus 로고
    • For reviews, see: and references cited therein
    • For reviews, see:. Glorius F. Org. Biomol. Chem. 3 (2005) 4171 and references cited therein
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 4171
    • Glorius, F.1
  • 3
    • 0011592742 scopus 로고    scopus 로고
    • For asymmetric hydrogenation of 2-methylquinoxaline, see:
    • For asymmetric hydrogenation of 2-methylquinoxaline, see:. Bianchini C., Barbaro P., and Scapacci G. J. Organomet. Chem. 621 (2001) 26
    • (2001) J. Organomet. Chem. , vol.621 , pp. 26
    • Bianchini, C.1    Barbaro, P.2    Scapacci, G.3
  • 14
    • 0000093414 scopus 로고
    • Trost B.M., and Fleming I. (Eds), Pergamon, Oxford
    • Keay J.D. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis vol. 8 (1991), Pergamon, Oxford 579
    • (1991) Comprehensive Organic Synthesis , vol.8 , pp. 579
    • Keay, J.D.1
  • 16
    • 34249294595 scopus 로고    scopus 로고
    • Barton D.H.R., Nakanishi K., and Meth-Cohn O. (Eds), Elsevier, Oxford
    • In: Barton D.H.R., Nakanishi K., and Meth-Cohn O. (Eds). Comprehensive Natural Products Chemistry (1999), Elsevier, Oxford 1-9
    • (1999) Comprehensive Natural Products Chemistry , pp. 1-9
  • 44
    • 34249282090 scopus 로고    scopus 로고
    • note
    • When the S/C is 1000/1, using KI and LiI as the additive, the conversions in THF are 37% and 34%, respectively.
  • 45
    • 34249294118 scopus 로고    scopus 로고
    • note
    • 2 as the metal precursor with the following chiral ligands in THF in the presence of iodine: (R,R)-Me-DuPhos, (R)-MeO-BiPhep and (R)-BINAP. These reactions gave product 2a with good yields, but the enantioselectivities were very low (<2% ee).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.