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Volumn 25, Issue 1, 1988, Pages 81-87

Directed lithiation of 4‐halopyridines: Chemoselectivity, regioselectivity and application to synthesis

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Indexed keywords


EID: 0001889003     PISSN: 0022152X     EISSN: 19435193     Source Type: Journal    
DOI: 10.1002/jhet.5570250112     Document Type: Article
Times cited : (52)

References (27)
  • 15
    • 0011553427 scopus 로고
    • 5-Aryl-1,3-dihydro-2H-pyrido-1,4-diazepin-2-ones
    • (4‐Amino‐3‐pyridyl)phenylmethanone (26) has been previously prepared in 8 steps from pyridine‐3,4 dicarboxylic acid in low yield by,. The same product was obtained by us in 3 steps from 4‐halopyridines in yields of 35–65
    • (1965) Journal of Medicinal Chemistry , vol.8 , pp. 722
    • Littel, R.1    Alien, D.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.