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Volumn 13, Issue 12, 2011, Pages 3032-3035

Direct aldol reactions catalyzed by a heterogeneous guanidinium salt/proline system under solvent-free conditions

Author keywords

[No Author keywords available]

Indexed keywords

3-HYDROXYBUTANAL; ALDEHYDE; ALDOL; AZABICYCLO DERIVATIVE; GUANIDINE; INORGANIC SALT; PROLINE; TRIAZABICYCLODECENE;

EID: 79958856343     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200890r     Document Type: Article
Times cited : (67)

References (52)
  • 1
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    • For some recent monographs and reviews, see:, Vol.;, Ed.; Wiley-VCH: Weinheim
    • For some recent monographs and reviews, see: Modern Aldol Reactions, Vol. 1-2; Mahrwald, Ed.; Wiley-VCH: Weinheim, 2004.
    • (2004) Modern Aldol Reactions , vol.12
    • Mahrwald1
  • 8
    • 0035886887 scopus 로고    scopus 로고
    • For some authoritative reviews on organocatalysis, see
    • For some authoritative reviews on organocatalysis, see: Dalko, P. I.; Moisan, L. Angew. Chem., Int. Ed. 2001, 40, 3726
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 3726
    • Dalko, P.I.1    Moisan, L.2
  • 23
    • 0345359331 scopus 로고    scopus 로고
    • For a high throughput screening of additives in organocatalyzed reactions, see
    • For a high throughput screening of additives in organocatalyzed reactions, see: Mase, N.; Tanaka, F.; Barbas, C. F. Org. Lett. 2003, 5, 4369
    • (2003) Org. Lett. , vol.5 , pp. 4369
    • Mase, N.1    Tanaka, F.2    Barbas, C.F.3
  • 44
    • 53849119486 scopus 로고    scopus 로고
    • The Liebscher group has reported improvements in (S)-proline catalyzed aldol reactions using guanidinium salts and ionic liquids as solvents
    • The Liebscher group has reported improvements in (S)-proline catalyzed aldol reactions using guanidinium salts and ionic liquids as solvents: Shah, J.; Blumenthal, B.; Yacob, Z.; Liebscher, J. Adv. Synth. Catal. 2008, 350, 1267
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 1267
    • Shah, J.1    Blumenthal, B.2    Yacob, Z.3    Liebscher, J.4
  • 46
    • 66149105445 scopus 로고    scopus 로고
    • For recent examples of aldol reactions carried out under solvent-free conditions, see
    • For recent examples of aldol reactions carried out under solvent-free conditions, see: Almasi, D.; Alonso, D. A.; Balaguer, A. N.; Najera, C. Adv. Synth. Catal. 2009, 351, 1123
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 1123
    • Almasi, D.1    Alonso, D.A.2    Balaguer, A.N.3    Najera, C.4
  • 51
    • 33846474978 scopus 로고    scopus 로고
    • For a discussion on the crystallization behaviour of proline and its role in asymmetric organocatalysis, see:, and references therein
    • For a discussion on the crystallization behaviour of proline and its role in asymmetric organocatalysis, see: Kellogg, R. M. Angew. Chem., Int. Ed. 2007, 46, 494 and references therein.
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 494
    • Kellogg, R.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.