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Volumn 72, Issue 25, 2007, Pages 9779-9781

Chiral bifunctional organocatalysts in asymmetric aza-Morita-Baylis-Hillman reactions of ethyl (arylimino)acetates with methyl vinyl ketone and ethyl vinyl ketone

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS; CHEMICAL REACTIONS; CHIRALITY; ENANTIOMERS;

EID: 36849076719     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo701764e     Document Type: Article
Times cited : (64)

References (38)
  • 1
    • 0342419508 scopus 로고    scopus 로고
    • For reviews of the Morita-Baylis-Hillman reaction, see: a
    • For reviews of the Morita-Baylis-Hillman reaction, see: (a) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001-8062.
    • (1996) Tetrahedron , vol.52 , pp. 8001-8062
    • Basavaiah, D.1    Rao, P.D.2    Hyma, R.S.3
  • 3
  • 14
    • 15744383666 scopus 로고    scopus 로고
    • and references cited therein
    • (f) Shi, M.; Chen, L.-H.; Li, C.-Q. J. Am. Chem. Soc. 2005, 127, 3790-3800 and references cited therein.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 3790-3800
    • Shi, M.1    Chen, L.-H.2    Li, C.-Q.3
  • 25
    • 0032556396 scopus 로고    scopus 로고
    • For selected papers regarding asymmetric MBH reactions, see: a
    • For selected papers regarding asymmetric MBH reactions, see: (a) Barrett, A. G. M.; Cook, A. S.; Kamimura, A. Chem. Commun. 1998, 2533-2534.
    • (1998) Chem. Commun , pp. 2533-2534
    • Barrett, A.G.M.1    Cook, A.S.2    Kamimura, A.3
  • 38
    • 36849063555 scopus 로고    scopus 로고
    • Ethyl (arylimino)acetates 1 are more moisture sensitive than N-sulfonated imines and N-phosphorated imines. It is necessary to remove any moisture by using molecular sieves 4Å.
    • Ethyl (arylimino)acetates 1 are more moisture sensitive than N-sulfonated imines and N-phosphorated imines. It is necessary to remove any moisture by using molecular sieves 4Å.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.