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Volumn 25, Issue 6-7, 2014, Pages 534-546

Doubly diastereoselective conjugate additions of the antipodes of lithium N-benzyl-N-(α-methylbenzyl)amide to enantiopure ε-O-protected α,β-unsaturated esters derived from d-ribose

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DIOXOLANE DERIVATIVE; ESTER; ISOASCORBIC ACID; LITHIUM DERIVATIVE; LITHIUM N BENZYL N ISOPROPYLAMIDE; REAGENT; RIBOSE; TARTARIC ACID; UNCLASSIFIED DRUG;

EID: 84898845940     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2014.02.004     Document Type: Article
Times cited : (15)

References (40)
  • 7
    • 24344501374 scopus 로고    scopus 로고
    • The antipodes of 2 are known to undergo conjugate addition to a range of achiral α,β-unsaturated esters (>250 examples) with uniformly high and predictable levels of diastereoselectivity (>95:5 dr). For reviews of this methodology, see
    • The antipodes of 2 are known to undergo conjugate addition to a range of achiral α,β-unsaturated esters (>250 examples) with uniformly high and predictable levels of diastereoselectivity (>95:5 dr). For reviews of this methodology, see: S.G. Davies, A.D. Smith, and P.D. Price Tetrahedron: Asymmetry 16 2005 2833
    • (2005) Tetrahedron: Asymmetry , vol.16 , pp. 2833
    • Davies, S.G.1    Smith, A.D.2    Price, P.D.3
  • 23
    • 79953165403 scopus 로고    scopus 로고
    • Based on our analogous one-pot transmetallation/ring-opening/Wadsworth- Emmons sequence of reactions; see
    • Based on our analogous one-pot transmetallation/ring-opening/Wadsworth- Emmons sequence of reactions; see: E.A. Brock, S.G. Davies, J.A. Lee, P.M. Roberts, and J.E. Thomson Org. Lett. 13 2011 1594
    • (2011) Org. Lett. , vol.13 , pp. 1594
    • Brock, E.A.1    Davies, S.G.2    Lee, J.A.3    Roberts, P.M.4    Thomson, J.E.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.