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Volumn 47, Issue 26, 2006, Pages 4403-4407

Microwave-promoted Suzuki-Miyaura cross-coupling of aryl halides with phenylboronic acid under aerobic conditions catalyzed by a new palladium complex with a thiosemicarbazone ligand

Author keywords

C C bond formation; Homogeneous catalysis; Microwave; Phosphine free ligand; Suzuki Miyaura cross coupling; Thiosemicarbazone

Indexed keywords

BENZENEBORONIC ACID; CHELATE; HALIDE; PALLADIUM COMPLEX; THIOSEMICARBAZONE;

EID: 33646779214     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.04.088     Document Type: Article
Times cited : (66)

References (60)
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    • Recent selected papers on the microwave-promoted Suzuki coupling:
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    • note
    • 2: C, 51.0; H, 5.5; N, 12.7; Pd, 16.1; S, 9.7. Found: C, 51.2; H, 5.6; N, 12.2; Pd, 16.0; S, 9.6.
  • 57
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    • note
    • w = 0.2670. All hydrogen atoms were located in their calculated positions (C-H 0.93-0.97 Å) and refined using a riding model, except hydrogen atom N(2)H which were located by difference maps and refined isotropically.
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    • note
    • 4, filtered, passed through Celite and analyzed by GC and GC-MS.
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    • Strauss, C. R. Microwave-assisted Organic Chemistry in Pressurized Reactors. In Ref. 7a, pp 35-60 and references quoted therein.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.