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Volumn 40, Issue 5, 2011, Pages 518-520

Asymmetric vinylogous michael reaction of α,β-unsaturated aldehyde with buteno-4-lactone

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EID: 79958222614     PISSN: 03667022     EISSN: 13480715     Source Type: Journal    
DOI: 10.1246/cl.2011.518     Document Type: Article
Times cited : (9)

References (40)
  • 23
    • 34547130040 scopus 로고    scopus 로고
    • For selected recent examples of γ-butenolide and its derivatives as nucleophiles: a) S. E. Denmark, J. R. Heemstra, J. Org. Chem. 2007, 72, 5668.
    • (2007) J. Org. Chem. , vol.72 , pp. 5668
    • Denmark, S.E.1    Heemstra, J.R.2
  • 24
    • 30744451484 scopus 로고    scopus 로고
    • Recent advances in vinylogous aldol reactions and their applications in the syntheses of natural products
    • DOI 10.1007/b96887, Natural Product Synthesis II: Targets, Methods, Concepts
    • b) M.Kalesse, Recent Advances in Vinylogous Aldol Reactions and Their Applications in the Syntheses of Natural Products in Natural Products Synthesis II: Targets, Methods, Concepts, ed. by J. Mulzer, 2005, Vol. 244, p. 43. doi:10.1007/b96887. (Pubitemid 44423484)
    • (2005) Topics in Current Chemistry , vol.244 , pp. 43-76
    • Kalesse, M.1
  • 39
    • 79958197262 scopus 로고    scopus 로고
    • note
    • 4 was introduced. The resulting solution was stirred for an additional 1 h at rt. The crude was filtered using sintered discs with silica gel. The filtration was evaporated under reduced pressure to remove the solvent. The residue was purified by silica gel chromatography to yield the desired product.
  • 40
    • 79958219540 scopus 로고    scopus 로고
    • Supporting Information is availableelectronically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lettindex.html.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.