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Volumn 20, Issue 38, 2014, Pages 12072-12082

Diphenylprolinol silyl ether catalyzed asymmetric Michael reaction of nitroalkanes and β,β-disubstituted α,β-unsaturated aldehydes for the construction of all-carbon quaternary stereogenic centers

Author keywords

asymmetric synthesis; enantioselectivity; isomerization; Michael addition; organocatalysis

Indexed keywords

ADDITION REACTIONS; ALDEHYDES; CARBON; CATALYSIS; ETHERS; ISOMERIZATION; ISOMERS; NITROGEN REMOVAL; PARAFFINS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 84912563672     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201403588     Document Type: Article
Times cited : (19)

References (68)
  • 1
    • 55049138759 scopus 로고    scopus 로고
    • (Ed.: P. I. Dalko), Wiley-VCH, Weinheim
    • Enantioselective Organocatalysis (Ed.:, P. I. Dalko,), Wiley-VCH, Weinheim, 2007
    • (2007) Enantioselective Organocatalysis
  • 36
    • 84887879802 scopus 로고    scopus 로고
    • Recently Wennemers and co-workers reported the asymmetric Michael reaction of aldehyde and β,β-disubstituted nitroalkene, which affords a similar product to the Michael reaction of nitroalkane and β,β-disubstituted α,β-unsaturated aldehyde. See
    • Recently Wennemers and co-workers reported the asymmetric Michael reaction of aldehyde and β,β-disubstituted nitroalkene, which affords a similar product to the Michael reaction of nitroalkane and β,β-disubstituted α,β-unsaturated aldehyde. See:, R. Kastl, H. Wennemers, Angew. Chem. 2013, 125, 7369
    • (2013) Angew. Chem. , vol.125 , pp. 7369
    • Kastl, R.1    Wennemers, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.