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Volumn 10, Issue 22, 2012, Pages 4424-4432

Erratum: Asymmetric synthesis of 2-alkyl-substituted tetrahydroquinolines by an enantioselective aza-Michael reaction (Organic and Biomolecular Chemistry (2012) 10 (4424-4432) DOI: 10.1039/c2ob25122a);Asymmetric synthesis of 2-alkyl-substituted tetrahydroquinolines by an enantioselective aza-Michael reaction

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; ETHYLENE; ETHYLENE GLYCOL; REACTION INTERMEDIATES;

EID: 84861312491     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/C3OB90163G     Document Type: Erratum
Times cited : (34)

References (39)
  • 5
    • 0041825591 scopus 로고    scopus 로고
    • The iodine additive can be replaced by a stoichiometric amount of chloroformate to give the N-protected quinoline. However, the level of enantioselectivity was somewhat lower
    • W. B. Wang S. M. Lu P. Y. Yang X. W. Han Y. G. Zhou J. Am. Chem. Soc. 2003 125 10536
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 10536
    • Wang, W.B.1    Lu, S.M.2    Yang, P.Y.3    Han, X.W.4    Zhou, Y.G.5
  • 26
    • 33845555256 scopus 로고
    • Without the Lewis acid the reaction yielded a mixture of products, including the partially reduced tetrahydroquinolin-4-ol
    • T. F. Buckley H. Rapoport J. Am. Chem. Soc. 1982 104 4446
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 4446
    • Buckley, T.F.1    Rapoport, H.2
  • 28
    • 46149140781 scopus 로고
    • Increasing the pressure of this reaction led to significant degradation of the product, possibly through the competitive reduction of the aromatic ring
    • K. Horita T. Yoshioka T. Tanaka Y. Oikawa O. Yonemitsu Tetrahedron 1986 42 3021
    • (1986) Tetrahedron , vol.42 , pp. 3021
    • Horita, K.1    Yoshioka, T.2    Tanaka, T.3    Oikawa, Y.4    Yonemitsu, O.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.