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Volumn , Issue 33, 2010, Pages 6423-6429

Direct access to cumbersome aminated quaternary centers by hyperbaric aza-Michael additions

Author keywords

Amines; Chirality; High pressure chemistry; Michael addition

Indexed keywords


EID: 78649312515     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201000984     Document Type: Article
Times cited : (22)

References (42)
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    • Cardillo, G.1    Tomasini, C.2
  • 8
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    • V. A. Soloshonok (Eds.), β-Amino Acids, Wiley, Hoboken, USA.
    • E. Juaristi, V. A. Soloshonok (Eds.), Enantioselective Synthesis of β-Amino Acids, Wiley, Hoboken, USA, 2005.
    • (2005) Enantioselective Synthesis of
    • Juaristi, E.1
  • 25
    • 37749043974 scopus 로고    scopus 로고
    • The dramatic influence of alcohols on the Michael reaction is highlighted in,. Similarly, the protonation of an aza-Baylis-Hillman intermediate by phenol is noted in, Synlett 2007, 3160 -3164.
    • The dramatic influence of alcohols on the Michael reaction is highlighted in, S. Shirakawa, S. Shimizu, Synlett 2007, 3160-3164. Similarly, the protonation of an aza-Baylis-Hillman intermediate by phenol is noted in, S. Shirakawa, S. Shimizu, Synlett 2007, 3160 -3164.
    • (2007) Synlett , pp. 3160-3164
    • Shirakawa, S.1    Shimizu, S.2    Shirakawa, S.3    Shimizu, S.4
  • 26
    • 78649313865 scopus 로고    scopus 로고
    • By contrast, lithium amides add diastereoselectively onto α, βdisubstituted α, βunsaturated esters
    • By contrast, lithium amides add diastereoselectively onto α, βdisubstituted α, βunsaturated esters
  • 33
    • 0000574863 scopus 로고    scopus 로고
    • The rate constant of this reaction is known to be accelerated in polar media.
    • The rate constant of this reaction is known to be accelerated in polar media:, G. Jenner, J. Phys. Org. Chem. 1999, 12, 619-625.
    • (1999) J. Phys. Org. Chem. , vol.12 , pp. 619-625
    • Jenner, G.1
  • 35
    • 33747214078 scopus 로고    scopus 로고
    • For a fruitful application of nitroolefins as aza-Michael acceptors, see.
    • For a fruitful application of nitroolefins as aza-Michael acceptors, see:, X. Deng, N. S. Mani, Org. Lett. 2006, 8, 3505-3508.
    • (2006) Org. Lett. , vol.8 , pp. 3505-3508
    • Deng, X.1    Mani, N.S.2
  • 38
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    • As observed in a similar case by.
    • As observed in a similar case by, G. Jenner, Tetrahedron Lett. 2001, 42, 4807-4810.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 4807-4810
    • Jenner, G.1
  • 39
    • 35748984895 scopus 로고    scopus 로고
    • references cited therein
    • See for instance G. Smitha, Ch. Sanjeeva Reddy, Catal. Commun. 2007, 8, 434-436 and references cited therein.
    • (2007) Catal. Commun. , vol.8 , pp. 434-436
    • Smitha, G.1    Reddy, C.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.