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Volumn 52, Issue 8, 2013, Pages 2160-2162

Mechanism of diphenylprolinol silyl ether catalyzed michael addition revisited - But still controversial

Author keywords

enantioselectivity; Michael reaction; organocatalysis; reaction mechanisms; reactive intermediates

Indexed keywords

CONJUGATE ADDITION; ENAMINES; EXPERIMENTAL DATUM; LINEAR ALDEHYDES; MICHAEL ADDITIONS; MICHAEL REACTIONS; NITROOLEFINS; ORGANOCATALYSIS; REACTION MECHANISM; REACTIVE INTERMEDIATE; RESEARCH GROUPS; SILYL ETHERS; TRIMETHYLSILYL; TWO VIEWS;

EID: 84873904037     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201207775     Document Type: Article
Times cited : (33)

References (17)
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    • In the original report, formation of the product enamine was suggested to be formed by rate-determining protonation of a minor species identified by NMR spectroscopy, the structure of which was later corrected:, J. Burés, A. Armstrong, D. G. Blackmond, J. Am. Chem. Soc. 2012, 134, 14264.
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 14264
    • Burés, J.1    Armstrong, A.2    Blackmond, D.G.3
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.