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Volumn 53, Issue 47, 2014, Pages 12822-12826

Catalytic Enantioselective Synthesis of Atropisomeric Biaryls: A Cation-Directed Nucleophilic Aromatic Substitution Reaction

Author keywords

aromatic substitution; atropisomerism; chirality; kinetic resolution; phase transfer catalysis

Indexed keywords

AROMATIC COMPOUNDS; AROMATIZATION; CATALYSIS; CHELATION; CHIRALITY; SUBSTITUTION REACTIONS;

EID: 84911429048     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201408205     Document Type: Article
Times cited : (117)

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    • samples which the enantiomers interconvert on the timescale of the HPLC, a raised plateau between the separate enantiomer peaks is present; no such effect was observed for 2. For a discussion of this effect, see.
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    • CCDC 1019025 (13) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre www.ccdc.cam.ac.uk/data-request/cif. We tentatively speculate that the absolute configuration of the major enantiomer of substrates in Table 2 is the same as that for 13. This configuration is consistent with the order of elution of the major enantiomer for 13-22 when using HPLC with a chiral stationary phase. However, absolute configuration of 14-22 cannot be unequivocally demonstrated with the data we possess.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.