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Volumn 51, Issue 38, 2010, Pages 4975-4980

Oxalyl chloride as carbonyl synthon in Pd-catalyzed carbonylations of triarylbismuth and triarylindium organometallic nucleophiles

Author keywords

Atom efficient; C1 synthon; Carbonylations; Oxalyl chloride; Palladium; Triarylbismuths; Triarylindiums

Indexed keywords

BENZOPHENONE; BIPHENYL; BISMUTH DERIVATIVE; CARBONYL DERIVATIVE; CHLORIDE; INDIUM; KETONE; NUCLEOPHILE; OXALYL CHLORIDE; PALLADIUM; UNCLASSIFIED DRUG;

EID: 78549294474     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.07.074     Document Type: Article
Times cited : (37)

References (41)
  • 17
    • 78549254619 scopus 로고    scopus 로고
    • Organobismuth Chemistry Suzuki H.,Matano Y. Eds.; Elsevier: Amsterdam
    • Organobismuth Chemistry; Suzuki, H., Matano, Y., Eds.; Elsevier: Amsterdam, 2001.
    • (2001)
  • 18
  • 25
    • 85030579339 scopus 로고    scopus 로고
    • 3N was found to be beneficial as an additive (Ref. 11)
    • 3N was found to be beneficial as an additive (Ref. 11).
  • 26
    • 85030579332 scopus 로고    scopus 로고
    • C NMR, IR, and HRMS studies
    • C NMR, IR, and HRMS studies.
  • 30
    • 85030587852 scopus 로고    scopus 로고
    • 3 reagents used for carbonylation studies were prepared by following the reported procedure.15c Indium(III) chloride (0.5 mmol, 0.1105 g) was placed in a round-bottomed flask with a stirring bar and heated with a heat gun under high vacuum for 0.5 h. Once it was completely dried, the flask was filled with nitrogen and re-evacuated. Then THF (5 mL) was added through a syringe. To this, ArMgBr (1.62 mmol) was added dropwise via a pressureequalizing funnel for about 1 h. The contents of the flask were allowed to stir for 0.5 h. The resultant triarylindium solution was directly used for carbonylation reactions using oxalyl chloride
    • 3 reagents used for carbonylation studies were prepared by following the reported procedure.15c Indium(III) chloride (0.5 mmol, 0.1105 g) was placed in a round-bottomed flask with a stirring bar and heated with a heat gun under high vacuum for 0.5 h. Once it was completely dried, the flask was filled with nitrogen and re-evacuated. Then THF (5 mL) was added through a syringe. To this, ArMgBr (1.62 mmol) was added dropwise via a pressureequalizing funnel for about 1 h. The contents of the flask were allowed to stir for 0.5 h. The resultant triarylindium solution was directly used for carbonylation reactions using oxalyl chloride.
  • 31
    • 85030587723 scopus 로고    scopus 로고
    • C NMR, IR, and HRMS studies
    • C NMR, IR, and HRMS studies.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.