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Volumn , Issue 1, 2009, Pages 51-54

Rapid 1,4-alkynylation of acyclic enones using K[F3BC≡CR]

Author keywords

Conjugated alkynylation; Enones; Potassium organotrifluoroborates

Indexed keywords


EID: 62449223633     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0028-1087481     Document Type: Article
Times cited : (11)

References (22)
  • 4
    • 62449155387 scopus 로고    scopus 로고
    • Based on a survey of the SciFinder Scholar ACS, September
    • Based on a survey of the SciFinder Scholar (ACS), CAPLUS and MEDLINE databases, September 2008.
    • (2008) CAPLUS and MEDLINE databases
  • 20
    • 39849091031 scopus 로고    scopus 로고
    • The nucleophile described in Equation 1 has been recently used by Tehrani and co-workers for the alkynylation of two imines. However, the corresponding products were obtained only in poor yields (17-31%). See: Stas, S.; Tehrani, K. A.; Laus, G. Tetrahedron 2008, 64, 3457.
    • The nucleophile described in Equation 1 has been recently used by Tehrani and co-workers for the alkynylation of two imines. However, the corresponding products were obtained only in poor yields (17-31%). See: Stas, S.; Tehrani, K. A.; Laus, G. Tetrahedron 2008, 64, 3457.
  • 21
    • 62449275281 scopus 로고    scopus 로고
    • α,β-Unsaturated esters were unreactive under the present conditions
    • α,β-Unsaturated esters were unreactive under the present conditions.
  • 22
    • 62449140104 scopus 로고    scopus 로고
    • +. 5-Methyl-7-phenylhept-6-yn-3-one (4ab, Entry 1, Table 2) Yield 70%. Yellow liquid.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.