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Volumn 21, Issue 9, 2015, Pages 3589-3595

Enantioselective organocatalytic reduction of β-trifluoromethyl nitroalkenes: An efficient strategy for the synthesis of chiral β-trifluoromethyl amines

Author keywords

Bifunctional catalyst; Chiral fluorinated amines; Nitroalkenes; Reduction; Trifluoromethyl derivatives

Indexed keywords

AMINES; AMINO ACIDS; CATALYSTS; ESTERIFICATION; ESTERS; REDUCTION;

EID: 84923061722     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201405730     Document Type: Article
Times cited : (34)

References (52)
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    • note
    • For experimental details on the synthesis and characterization of the catalysts, see the Supporting Information.
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    • note
    • In fact, a change in the diastereoisomeric ratio of the two isomers, from roughly 50:50 to 90:10 was observed for all compounds 16a-c to take place in few days, even when the isomeric mixture was kept neat at 8°C.
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    • note
    • See ref. [7a]. The reactions sequence did not affect the stereochemical integrity of the starting material, as confirmed by HPLC analysis on a chiral stationary phase (Supporting Information).
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    • note
    • We thank the referee for the nice suggestion to consider also this type of interaction.
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    • note
    • For further details on the computational studies see the Supporting Information.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.