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Volumn 9, Issue 6, 2011, Pages 1784-1790

Highly enantioselective synthesis of syn-aldols of cyclohexanones via chiral primary amine catalyzed asymmetric transfer aldol reactions in ionic liquid

Author keywords

[No Author keywords available]

Indexed keywords

ALDOL REACTIONS; ASYMMETRIC TRANSFER; CYCLOHEXANONES; ENANTIOSELECTIVE SYNTHESIS; KINETIC RESOLUTION; PRIMARY AMINES; SYN-ALDOLS;

EID: 79952124240     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c0ob00682c     Document Type: Article
Times cited : (16)

References (47)
  • 4
    • 77951529935 scopus 로고    scopus 로고
    • For reviews on chiral amine catalyzed direct aldol reactions, see:
    • B. M. Trost C. S. Brindle Chem. Soc. Rev. 2010 39 1600 632
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 1600-632
    • Trost, B.M.1    Brindle, C.S.2
  • 12
    • 49649083136 scopus 로고    scopus 로고
    • For selected examples on primary aldol catalyzed aldol reaction, see
    • Y.-C. Chen Synlett 2008 1919
    • (2008) Synlett , pp. 1919
    • Chen, Y.-C.1
  • 23
    • 22944480542 scopus 로고    scopus 로고
    • During the preparation of this manuscript, Blanchet and coworkers reported Brønsted acid catalyzed syn diastereoselective asymmetric aldol reaction, but with moderate enantioselectivity, see:
    • H.-J. Li H.-Y. Tian Y.-C. Wu Y.-J. Chen L. Liu D. Wang C.-J. Li Adv. Synth. Catal. 2005 347 1247 1256
    • (2005) Adv. Synth. Catal. , vol.347 , pp. 1247-1256
    • Li, H.-J.1    Tian, H.-Y.2    Wu, Y.-C.3    Chen, Y.-J.4    Liu, L.5    Wang, D.6    Li, C.-J.7
  • 36
    • 68349143232 scopus 로고    scopus 로고
    • Currently, syn-aldols derived from aliphatic aldehyde are not easily accessed and a facile racemic preparation itself would require future method development, for an example, see:
    • S. Luo L. Zhang J.-P. Cheng Chem.-Asian J. 2009 4 1184 1195
    • (2009) Chem.-Asian J. , vol.4 , pp. 1184-1195
    • Luo, S.1    Zhang, L.2    Cheng, J.-P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.