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Volumn , Issue 46, 2008, Pages 6242-6244

Primary amino acid lithium salt as a catalyst for asymmetric Michael addition of isobutyraldehyde with β-nitroalkenes

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; AMINO ACID; BETA NITROALKENE DERIVATIVE; ISOBUTYRALDEHYDE; LITHIUM SALT; UNCLASSIFIED DRUG;

EID: 56849110812     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b814804j     Document Type: Article
Times cited : (67)

References (35)
  • 3
    • 4143094833 scopus 로고    scopus 로고
    • A special issue on asymmetric organocatalysis
    • A special issue on asymmetric organocatalysis Acc. Chem. Res. 2004 37 487
    • (2004) Acc. Chem. Res. , vol.37 , pp. 487
  • 4
    • 47749122232 scopus 로고    scopus 로고
    • Wiley-VCH, Weinheim, A review on organocatalysis using a primary amino acid was published recently, see:
    • A. Berkessel and H. Gröger, Asymmetric Organocatalysis, Wiley-VCH, Weinheim, 2005
    • (2005) Asymmetric Organocatalysis
    • Berkessel, A.1    Gröger, H.2
  • 5
    • 44949251617 scopus 로고    scopus 로고
    • Review on asymmetric Michael additions to nitroalkenes:
    • L.-W. Xu Y. Lu Org. Biomol. Chem. 2008 6 2047
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 2047
    • Xu, L.-W.1    Lu, Y.2
  • 11
    • 33645036848 scopus 로고    scopus 로고
    • Organocatalytic asymmetric Michael addition of α-branched carbonyl compounds with nitroalkenes:
    • S. B. Tsogoeva S. Wei Chem. Commun. 2006 1451
    • (2006) Chem. Commun. , pp. 1451
    • Tsogoeva, S.B.1    Wei, S.2
  • 28
    • 33747205615 scopus 로고    scopus 로고
    • Yamaguchi reported l-proline rubidium salt was effective in the Michael addition of malonate with α,β-unsaturated ketones or α,β-unsaturated aldehydes, although lithium salts of l-proline and l-valine gave poor results:
    • S. Mossé A. Alexakis Org. Lett. 2006 8 3577
    • (2006) Org. Lett. , vol.8 , pp. 3577
    • Mossé, S.1    Alexakis, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.