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Volumn 356, Issue 11-12, 2014, Pages 2661-2670

The first allylation of esters by an allylsilane: One-pot domino synthesis of triallylmethane derivatives

Author keywords

allylation; allylsilanes; esters; Lewis acids; triallylmethanes

Indexed keywords


EID: 84906075788     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201400296     Document Type: Article
Times cited : (4)

References (51)
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    • Esters remain unaffected during the Sakurai reaction, see.
    • Esters remain unaffected during the Sakurai reaction, see:, P. A. Robertson, J. A. Katzenellenbogen, J. Org. Chem. 1983, 48, 5288-5302.
    • (1983) J. Org. Chem. , vol.48 , pp. 5288-5302
    • Robertson, P.A.1    Katzenellenbogen, J.A.2
  • 17
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    • using Sm reagents.
    • using Sm reagents:, Z. Li, Y. Zhang, Tetrahedron 2002, 58, 5301-5306.
    • (2002) Tetrahedron , vol.58 , pp. 5301-5306
    • Li, Z.1    Zhang, Y.2
  • 23
  • 36
    • 34250872268 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 3296-3299.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 3296-3299
  • 43
    • 0141757166 scopus 로고    scopus 로고
    • 4 with the ester carbonyl group, additional coordination with an appropriate neighbouring substituent might increase the electrophilic character of the ester carbonyl and facilitate nucleophilic attack by the allylsilane.
    • 4 with the ester carbonyl group, additional coordination with an appropriate neighbouring substituent might increase the electrophilic character of the ester carbonyl and facilitate nucleophilic attack by the allylsilane.
    • (2003) Chem. Eur. J. , vol.9 , pp. 4405-4413
    • Hanawa, H.1    Uraguchi, D.2    Konishi, S.3    Hashimoto, T.4    Maruoka, K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.