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Volumn 5, Issue 10, 2015, Pages 5927-5931

Organocatalytic Enantioselective Alkylation of Aldehydes with [Fe(bpy)3]Br2 Catalyst and Visible Light

Author keywords

aldehydes; organocatalysis; photocatalysis; radicals; stereoselective alkylations; Fe(bpy)3 Br2

Indexed keywords

ALDEHYDES; ALKYLATION; BROMINE COMPOUNDS; CARBONYL COMPOUNDS; CATALYSIS; CATALYSTS; ENANTIOSELECTIVITY; LIGHT; PHOTOCATALYSIS; RUBIDIUM COMPOUNDS; STEREOSELECTIVITY;

EID: 84943153031     PISSN: 21555435     EISSN: None     Source Type: Journal    
DOI: 10.1021/acscatal.5b01573     Document Type: Article
Times cited : (149)

References (44)
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    • 2 is not decomposed or oxidized during the reaction. As possible steps for the reduction of Fe(III) to Fe(II), we propose that the α-aminoalkyl radical produced after the addition of the malonate, or the oxidation of sacrificial enamine are the compelling reductants. For SOMO chemistry performed with Fe polypyridyl complexes in which Fe(III) complexes are used as stoichiometric oxidants of enamines, see: Comito, R. J.; Finelli, F. G.; MacMillan, D. W. C. J. Am. Chem. Soc. 2013, 135, 9358-9361 10.1021/ja4047312
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 9358-9361
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.