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Volumn 48, Issue 34, 2007, Pages 5938-5941

An approach toward oxidopyrylium ylides using Rh(II)-catalyzed cyclization chemistry

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DIOXOLANE DERIVATIVE; 2 DIAZO 3,6 DIOXO 6 PHENYLHEXENOIC ACID METHYL ESTER; 5 PHENYL FURAN 2,3 DIONE; CARBONYL DERIVATIVE; FURAN; OXIDE; OXIDOPYRYLIUM YLIDE DERIVATIVE; RHODIUM; UNCLASSIFIED DRUG;

EID: 34447649170     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.06.118     Document Type: Article
Times cited : (15)

References (63)
  • 29
  • 57
    • 34447651375 scopus 로고    scopus 로고
    • note
    • The reaction of 4 with a number of Rh(II) catalysts in several solvents and at different concentrations using diverse trapping agents only led to varying quantities of dimer 22 together with a tarry residue, which resisted purification. Our attempts to obtain an X-ray crystal structure of dimer 22 also failed due to the amorphous nature of the solid.
  • 58
    • 0005774435 scopus 로고
    • For some examples of 1,3-dioxole formation during the decomposition of diazocarbonyl compounds in the presence of simple aldehydes and ketones, see:
    • For some examples of 1,3-dioxole formation during the decomposition of diazocarbonyl compounds in the presence of simple aldehydes and ketones, see:. Weigand F., Dworschak H., Koch K., and Konstas S. Angew. Chem. 73 (1961) 409
    • (1961) Angew. Chem. , vol.73 , pp. 409
    • Weigand, F.1    Dworschak, H.2    Koch, K.3    Konstas, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.