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Volumn 78, Issue 4, 2013, Pages 1559-1575

Achieving control over the branched/linear selectivity in palladium-catalyzed allylic amination

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLIC AMINATION; ALLYLIC AMINES; ELECTROPHILES; ISOMERIZATION PATHWAYS; PALLADIUM CATALYST; PALLADIUM-CATALYZED; PALLADIUM-CATALYZED REACTIONS; PROTIC ACIDS; RING CLOSING METATHESIS;

EID: 84873968777     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3025253     Document Type: Article
Times cited : (40)

References (96)
  • 26
    • 0025232768 scopus 로고
    • Hayashi obtained high selectivities for branched products with palladium in the presence of a 2.5-fold excess of benzylamine: Hayashi, T.; Kishi, K.; Yamamoto, A.; Ito, Y. Tetrahedron Lett. 1990, 31, 1743
    • (1990) Tetrahedron Lett. , vol.31 , pp. 1743
    • Hayashi, T.1    Kishi, K.2    Yamamoto, A.3    Ito, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.