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Volumn 51, Issue 45, 2010, Pages 5889-5891

Rapid synthesis of cyclobutene diesters using a microwave-accelerated ruthenium-catalysed [2+2] cycloaddition

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; CYCLOBUTANE DERIVATIVE; CYCLOBUTENE; ESTER DERIVATIVE; RUTHENIUM; UNCLASSIFIED DRUG;

EID: 77957759629     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.08.119     Document Type: Article
Times cited : (26)

References (80)
  • 76
    • 77957816769 scopus 로고    scopus 로고
    • note
    • 1H NMR spectroscopy. The crude product was purified by column chromatography (1:1 EtOAc/petroleum spirits) to afford the pure product in the yield stated.
  • 77
    • 77957812960 scopus 로고    scopus 로고
    • See Supplementary data for temperature, pressure, and power profiles for this reaction
    • See Supplementary data for temperature, pressure, and power profiles for this reaction.
  • 78
    • 0000152667 scopus 로고
    • For the reaction of quadricyclane with DMAD, see: C.D. Smith J. Am. Chem. Soc. 88 1966 4273 4274. Yields of the second addition of DMAD to form 10 are typically modest: see Ref. 8d
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 4273-4274
    • Smith, C.D.1
  • 79
    • 77957765325 scopus 로고    scopus 로고
    • Mitsudo, in Ref. 8d, reported <10% yield of 10 using the twin addition approach from norbornadiene
    • Mitsudo, in Ref. 8d, reported <10% yield of 10 using the twin addition approach from norbornadiene.
  • 80
    • 77957803967 scopus 로고    scopus 로고
    • The reaction was trialled using diphenylacetylene as the alkyne partner, however, only a trace of the desired product was detected in the crude reaction mixture
    • The reaction was trialled using diphenylacetylene as the alkyne partner, however, only a trace of the desired product was detected in the crude reaction mixture.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.