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Volumn 70, Issue 12, 2005, Pages 4897-4900

Novel α,α-difluorohomophthalimides via copper-catalyzed tandom cross-coupling-cyclization of 2-halobenzamides with α,α-difluoro reformatskii reagent

Author keywords

[No Author keywords available]

Indexed keywords

PROTONS; REACTION KINETICS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EID: 20344370967     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050599r     Document Type: Article
Times cited : (33)

References (31)
  • 21
    • 20344379097 scopus 로고    scopus 로고
    • note
    • The yield of zinc reagent 3 in DMF was estimated to be ca. 75% according to the deuteriolysis of the zinc reagent 3, and less than 10% of homocoupling product was obtained (GC-MS analysis).
  • 25
    • 20344381209 scopus 로고    scopus 로고
    • note
    • In contrast to model studies with 2-bromobenzamides lacking any additional electron withdrawing group on the ring, copper-mediated nucleophilic addition of 3 to 2-bromo-5-nitrobenzamide was found to afford high yields of the expected cross-coupling reaction products.
  • 29
    • 0003033213 scopus 로고
    • (c) Cookson, R. F. Chem. Rev. 1974, 74, 5. See Supporting Information for details.
    • (1974) Chem. Rev. , vol.74 , pp. 5
    • Cookson, R.F.1
  • 30
    • 20344408434 scopus 로고    scopus 로고
    • note
    • a, of 10 and other compounds were calculated with Daylight software from Daylight Chemical Information Systems, Inc.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.