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Volumn 353, Issue 6, 2011, Pages 860-864

An easy entry to optically active spiroindolinones: Chiral Brønsted acid-catalysed Pictet-Spengler reactions of isatins

Author keywords

asymmetric catalysis; Br nsted acids; organocatalysis; Pictet Spengler reaction; spirooxindoles

Indexed keywords


EID: 79955443470     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201100050     Document Type: Article
Times cited : (143)

References (78)
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    • See the Supporting Information for details.
    • See the Supporting Information for details.
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    • for computational proof of this interaction, see
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    • For examples of chiral phosphoric acid-catalyzed asymmetric reactions involving N-alkylindoles and pyrroles, see
    • For examples of chiral phosphoric acid-catalyzed asymmetric reactions involving N-alkylindoles and pyrroles, see: M. Rueping, B. J. Nachtsheim, S. A. Moreth, M. Bolte, Angew. Chem. 2008, 120, 603-606
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    • In Pictet-Spengler reactions of dopamine taking place in biological settings, isotopic effects have shown that proton-transfer process causing re-aromatisation, assisted by a carboxylate enzyme basic residue, is partially rate-determining in the overall reaction. See.
    • In Pictet-Spengler reactions of dopamine taking place in biological settings, isotopic effects have shown that proton-transfer process causing re-aromatisation, assisted by a carboxylate enzyme basic residue, is partially rate-determining in the overall reaction. See:, L. Y. P. Luk, S. Bunn, D. K. Liscombe, P. J. Facchini, M. E. Tanner, Biochemistry 2007, 46, 10153-10161.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.