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Volumn 52, Issue 36, 2013, Pages 9495-9499

Functionalized alkenylzinc reagents bearing carbonyl groups: Preparation by direct metal insertion and reaction with electrophiles

Author keywords

aldehydes; lithium chloride; magnesium; organozinc reagents; zinc

Indexed keywords

CARBONYL GROUPS; CROSS-COUPLINGS; FUNCTIONALIZATION REACTIONS; FUNCTIONALIZED; LITHIUM CHLORIDE; METAL INSERTION; ORGANOZINC REAGENTS; POLYFUNCTIONAL COMPOUNDS;

EID: 84883231543     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201302058     Document Type: Article
Times cited : (34)

References (63)
  • 38
  • 58
    • 0027464132 scopus 로고
    • In the absence of LiCl, the iodo-derivative was required to achieve a zinc insertion
    • In the absence of LiCl, the iodo-derivative was required to achieve a zinc insertion:, R. C. Janakiram, Tetrahedron 1993, 49, 29.
    • (1993) Tetrahedron , vol.49 , pp. 29
    • Janakiram, R.C.1
  • 62
    • 77953935511 scopus 로고    scopus 로고
    • In our case, no addition has been observed due to reduced nucleophilicity of the chelated carbonyl groups
    • Angew. Chem. Int. Ed. 2010, 49, 4665. In our case, no addition has been observed due to reduced nucleophilicity of the chelated carbonyl groups.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 4665


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.