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Volumn , Issue 16, 1999, Pages 2233-2234

Chemoselective alkoxycarbonylation reagent having trifluoromethylsulfonyI-4-trifluoromethylaniIide as a leaving group

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Indexed keywords


EID: 0001529759     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a905561d     Document Type: Article
Times cited : (13)

References (21)
  • 10
    • 33746432833 scopus 로고    scopus 로고
    • MM2 calculation of 1 indicates dihedral angle 48° for (O=)C-NC=C(Ph).
    • MM2 calculation of 1 indicates dihedral angle 48° for (O=)C-NC=C(Ph).
  • 11
    • 33746397326 scopus 로고    scopus 로고
    • 1972, 144, 183 (Chem. Abstr., 78, 93525y).
    • A. F. Yapel, Jr., Adv. Chem. Ser., 1972, 144, 183 (Chem. Abstr., 78, 93525y).
    • Jr., Adv. Chem. Ser.
    • Yapel, A.F.1
  • 15
    • 33746441786 scopus 로고    scopus 로고
    • Treatment of 1 with lithium chloride in THF under reflux for 24 h led to decarboxylation to give N-benzyl-N-(triluoromethylsulfonyl)-4-trifluoromethyIanilide in 89% yield.
    • Treatment of 1 with lithium chloride in THF under reflux for 24 h led to decarboxylation to give N-benzyl-N-(triluoromethylsulfonyl)-4-trifluoromethyIanilide in 89% yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.