메뉴 건너뛰기




Volumn 14, Issue 6, 2010, Pages 1299-1303

Scaleable preparation of sensitive functionalized aromatics and heteroaromatics via directed metalation using tmpZnCl.LiCl

Author keywords

[No Author keywords available]

Indexed keywords

ACYLATIONS; AQUEOUS PHASE; CROSS COUPLING REACTIONS; ELECTROPHILES; FUNCTIONALIZED; HETEROAROMATICS; METALATION REACTION; METALATIONS; NITRO GROUP; SCALEABLE; ZINC REAGENTS; ZINCATION;

EID: 78649671754     PISSN: 10836160     EISSN: 1520586X     Source Type: Journal    
DOI: 10.1021/op1001935     Document Type: Article
Times cited : (37)

References (54)
  • 41
    • 65249111732 scopus 로고    scopus 로고
    • TMPZnCl.LiCl is commercially available from Chemetall Frankfurt/Germany (contact:).; Synlett 2010, 304
    • Mosrin, M.; Knochel, P. Org. Lett. 2009, 11, 1837 TMPZnCl.LiCl is commercially available from Chemetall Frankfurt/Germany (contact: christoph.krinninger@chemetall.com). Monzon, G.; Knochel, P. Synlett 2010, 304
    • (2009) Org. Lett. , vol.11 , pp. 1837
    • Mosrin, M.1    Knochel, P.2    Monzon, G.3    Knochel, P.4
  • 50
    • 78649641000 scopus 로고    scopus 로고
    • The relatively high catalyst loading was used to obtain fast conversions to the arylated arenes and heteroarenes to afford higher yields. Cross-coupling reactions with aryl bromides lead to decomposition of the corresponding zinc intermediates
    • The relatively high catalyst loading was used to obtain fast conversions to the arylated arenes and heteroarenes to afford higher yields. Cross-coupling reactions with aryl bromides lead to decomposition of the corresponding zinc intermediates.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.