메뉴 건너뛰기




Volumn 8, Issue 24, 2006, Pages 5673-5676

Highly functionalized benzene syntheses by directed mono or multiple magnesiations with TMPMgCl·LiCl

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE; BENZOPHENONE DERIVATIVE; CARBAMIC ACID DERIVATIVE; COPPER; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; KETONE; LITHIUM CHLORIDE; MAGNESIUM;

EID: 33846031566     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0625536     Document Type: Article
Times cited : (148)

References (54)
  • 24
  • 36
    • 33846000403 scopus 로고    scopus 로고
    • Knochel, P.; Dohle, W.; Gommermann, N.; Kneisel, F.; Kopp, F.; Korn, T.; Sapountzis, I.; Vu, V. A. Angew. Chem., Int. Ed. 2003, 42, 4302. (b) Knochel, P.; Krasovskiy, A.; Sapountzis, I. Handbook of Functionalized Organometattics; Knohel, P., Ed.; Wiley-VCH: Weinheim, Germany, 2005; 1, p 109.
    • (a) Knochel, P.; Dohle, W.; Gommermann, N.; Kneisel, F.; Kopp, F.; Korn, T.; Sapountzis, I.; Vu, V. A. Angew. Chem., Int. Ed. 2003, 42, 4302. (b) Knochel, P.; Krasovskiy, A.; Sapountzis, I. Handbook of Functionalized Organometattics; Knohel, P., Ed.; Wiley-VCH: Weinheim, Germany, 2005; Vol. 1, p 109.
  • 38
    • 33845989212 scopus 로고    scopus 로고
    • The conversion of the starting material is very slow even at 25 °C and no desired magnesiated product is observed.
    • (a) The conversion of the starting material is very slow even at 25 °C and no desired magnesiated product is observed.
  • 42
    • 33845965806 scopus 로고    scopus 로고
    • Interestingly, a OBoc-group cannot be used to direct lithiation due to its sensitivity toward organolithium reagents and various lithium bases
    • Interestingly, a OBoc-group cannot be used to direct lithiation due to its sensitivity toward organolithium reagents and various lithium bases.
  • 43
    • 33845996686 scopus 로고    scopus 로고
    • See the Supporting Information
    • See the Supporting Information.
  • 53
    • 33646065681 scopus 로고
    • See also the formation of sulfones
    • See also the formation of sulfones: Gilman, H.; Fothergill, R. E. J. Am. Chem. Soc. 1929, 51, 3501.
    • (1929) J. Am. Chem. Soc , vol.51 , pp. 3501
    • Gilman, H.1    Fothergill, R.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.