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Volumn 48, Issue 46, 2007, Pages 8213-8216

A novel strategy for the expeditious synthesis of aryl-tethered highly congested 2-hydroxybenzyl alcohols from 2-pyranones

Author keywords

1,3 Dibenzyloxy 2 propanone; 2 Hydroxy benzyl alcohol; Ring transformation

Indexed keywords

1,3 DIBENZYLOXYPROPAN 2 ONE; 2 PYRONE DERIVATIVE; ACETONE; ALCOHOL DERIVATIVE; BENZYL DERIVATIVE; BORON DERIVATIVE; BORON TRICHLORIDE; CHLORIDE; CYANIDE; SALIGENIN; UNCLASSIFIED DRUG;

EID: 35348842895     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.09.082     Document Type: Article
Times cited : (5)

References (30)
  • 30
    • 35348868739 scopus 로고    scopus 로고
    • note
    • General procedure for the synthesis of 2-benzyloxy-3-benzyloxymethyl-5-sec-aminobiphenyl-4-carbonitriles 3a-e: An equimolar mixture of 1a (344 mg, 1.0 mmol) and 2 (270 mg, 1.0 mmol) was stirred in a suspension of powdered KOH (207 mg, 1.5 mmol) in DMF (10 mL) for 2 h at room temperature. The reaction mixture was diluted with distilled water and the precipitate was filtered. The crude product was purified on a silica gel column using DCM as eluent.(...)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.