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Volumn 50, Issue 17, 2011, Pages 3920-3924

Oxidative and enantioselective cross-coupling of aldehydes and nitromethane catalyzed by diphenylprolinol silyl ether

Author keywords

asymmetric catalysis; cross coupling; one pot reaction; organocatalysis; oxidative reaction

Indexed keywords

ASYMMETRIC CATALYSIS; CROSS-COUPLING; ONE-POT REACTION; ORGANOCATALYSIS; OXIDATIVE REACTION;

EID: 79954614511     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201006885     Document Type: Article
Times cited : (125)

References (71)
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    • Recently, a Saegusa-type reaction was reported
    • Recently, a Saegusa-type reaction was reported
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    • As the transformation of aldehdye into α,β-unsaturated aldehyde is a synthetically important reaction, we investigated the oxidation using an achiral amine catalyst
    • As the transformation of aldehdye into α,β-unsaturated aldehyde is a synthetically important reaction, we investigated the oxidation using an achiral amine catalyst.
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    • For example, when 50 mol% of TEMPO was employed, cinnamaldehyde was obtained in 60% yield with the recovery of 3-phenylpropanal in 32% yield. As DDQ and TEMPO are gradually consumed, the yield of cinnamaldehyde decreases
    • For example, when 50 mol% of TEMPO was employed, cinnamaldehyde was obtained in 60% yield with the recovery of 3-phenylpropanal in 32% yield. As DDQ and TEMPO are gradually consumed, the yield of cinnamaldehyde decreases.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.