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Volumn 33, Issue 31, 1992, Pages 4439-4442

Organomanganese (II) reagents XXIII: Manganese-catalyzed acylation of organomagnesium compounds by car☐ylic acid chlorides

Author keywords

[No Author keywords available]

Indexed keywords

KETONE;

EID: 0026683208     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)60104-1     Document Type: Article
Times cited : (49)

References (10)
  • 6
    • 84918702357 scopus 로고    scopus 로고
    • 2 (1.5 mmol) and LiCl (3 mmol) in 50 ml of THF was stirred at room temperature until complete dissolution of the salts. A THF solution of HeptMgCl (1.5 M, 50 mmol) was then added in 30 min. at 0–10°C.It is advised to introduce the Grignard with a mechanical pump to control efficiently the addition rate. The reaction mixture was then stirred for 10 min. and the ketone BuCOHept was isolated by distillation after a usual work-up (1M HCl hydrolysis).
  • 7
    • 84918686839 scopus 로고    scopus 로고
    • [[Note]]
  • 8
    • 84918691354 scopus 로고    scopus 로고
    • 4COBu 89%
  • 9
    • 84918707828 scopus 로고    scopus 로고
    • It is already known that, in some cases, the acylation of RMnCl in THF gives better yields in the presence of a catalytic amount of copper chloride (see ref. 3).
  • 10
    • 84918674293 scopus 로고    scopus 로고
    • We have verified that this result cannot be obtained in the presence of copper (I or II) chloride alone.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.