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Volumn , Issue 19, 2008, Pages 3053-3057

Zinc(II) iodide-triethylsilane: A novel mild reduction system for direct deoxygenation of aryl aldehydes, ketones, and α,β-unsaturated enones

Author keywords

Carbonyl compounds; Deoxygenation; Hydrocarbons; Ionic hydrogenation; Zinc iodide

Indexed keywords

ALDEHYDE; CARBONYL DERIVATIVE; HYDROCARBON; IODINE; KETONE; ZINC;

EID: 57649133957     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0028-1083627     Document Type: Article
Times cited : (14)

References (34)
  • 19
    • 57649116889 scopus 로고    scopus 로고
    • Deng, G.; Zhao, X. L.; Li, Z.; Jiang, B.; Li, Y. C. unpublished results.
    • Deng, G.; Zhao, X. L.; Li, Z.; Jiang, B.; Li, Y. C. unpublished results.
  • 24
    • 57649131928 scopus 로고    scopus 로고
    • General Procedure for the Synthesis of Product 2: To a stirred solution of substrate 1(1 mmol) in 1,2-dichloroethane (5 mL) at r.t. was added solid zinc iodide (638 mg, 2 mmol).Then, triethylsilane (1.9 mL, 10 mmol) was added slowly to the above suspension via a syringe. The reaction mixture was stirred at r.t. until 1 was completely disappeared or there was no further conversion (TLC inspection, The stirring was stopped, and then the reaction mixture was filtered through Celite. The Celite was washed with CH 2Cl2 4 x 15 mL, The combined filtrate was washed with H2O and sat. brine, and then dried over anhyd Na2SO 4. After concentration, the residue was chromatographed on silica gel, eluting with 0-25% EtOAc in cyclohexane
    • 4. After concentration, the residue was chromatographed on silica gel, eluting with 0-25% EtOAc in cyclohexane.
  • 25
    • 57649133180 scopus 로고    scopus 로고
    • 3: 339.1033; found: 339.1041.
    • 3: 339.1033; found: 339.1041.
  • 28
    • 57649133576 scopus 로고    scopus 로고
    • 4: 274.1205; found: 274.1200.
    • 4: 274.1205; found: 274.1200.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.