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Volumn 48, Issue 39, 2007, Pages 6958-6961

Indium- and zinc-mediated Barbier-type allylations of an N,N-(dimethylsulfamoyl)-protected aldimine and subsequent deprotection

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; ALLYL BROMIDE DERIVATIVE; BROMINE DERIVATIVE; IMINE; INDIUM; N HOMOALLYLIC SULFANAMIDE DERIVATIVE; N,N (DIMETHYLSULFAMOYL) ALDIMINE; N,N (DIMETHYLSULFAMOYL) BENZALDIMINE; N,N (DIMETHYLSULFAMOYL) PROTECTED ALDIMINE; PIPERIDINE DERIVATIVE; TETRAHYDROPYRIDINE; UNCLASSIFIED DRUG; ZINC;

EID: 34548225502     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.07.167     Document Type: Article
Times cited : (19)

References (56)
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    • note
    • 4. After evaporation, the crude product was purified by flash chromatography (eluent: 20% EtOAc in hexane). For analytical data, see Supplementary data.
  • 52
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    • note
    • 4 and evaporation gave 3 (92%) as a light yellow oil. For analytical data, see Supplementary data.
  • 54
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    • note
    • 2 (0.3 mL) was prepared. The solution of 4 was cooled on an ice bath and treated dropwise with the catalyst solution over a period of 5 min. The reaction mixture was removed from the ice bath, allowed to warm to room temperature and stirred overnight. After 12 h, the product was purified by flash chromatography by passing the reaction mixture through a silica gel column affording 5 (25.5 mg, 91%) as a light yellow oil. For analytical data, see Supplementary data.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.