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Volumn 2, Issue 9, 2010, Pages 1122-1129

A Theoretical Study of the Mechanism of the Desymmetrization of Cyclic meso-Anhydrides by Chiral Amino Alcohols

Author keywords

Anhydrides; Asymmetric catalysis; Density functional theory; Modeling; Organocatalysis

Indexed keywords


EID: 79953216628     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.201000065     Document Type: Article
Times cited : (20)

References (48)
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    • Zipse and co-workers have also calculated the benzhydryl cation and benzyl cation affinities of quinine and its building blocks at the MP2(FC)/6-31+G(2d,p)//B3LYP/6-31G(d) level to explore why benzyl bromide reacts selectively at the Nsp3 center of cinchona alkaloids while benzhydrylium ions react selectively at the Nsp2 center.
    • Zipse and co-workers have also calculated the benzhydryl cation and benzyl cation affinities of quinine and its building blocks at the MP2(FC)/6-31+G(2d, p)//B3LYP/6-31G(d) level to explore why benzyl bromide reacts selectively at the Nsp3 center of cinchona alkaloids while benzhydrylium ions react selectively at the Nsp2 center. M. Baidya, M. Horn, H. Zipse, H. Mayr, J. Org. Chem. 2009, 74, 7157-7164.
    • (2009) J. Org. Chem. , vol.74 , pp. 7157-7164
    • Baidya, M.1    Horn, M.2    Zipse, H.3    Mayr, H.4
  • 35
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    • dissertation at RWTH Aachen University
    • T. Rantanen, dissertation at RWTH Aachen University, 2007.
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    • Rantanen, T.1
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.