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Volumn 56, Issue 23, 2015, Pages 3463-3467

A silver(I)-catalyzed intramolecular Ficini's [2+2] cycloaddition employing ynamides This Letter is dedicated to Professor Harry H. Wasserman with the deepest respect and admiration to honor his lifelong contribution and stewardship to Tetrahedron Publications and the field of Organic Chemistry

Author keywords

AgNTf2< inf>; Electrocyclic ring opening; Intramolecular 2+2 cycloaddition; The Ficini reaction; Ynamides

Indexed keywords

AMIDE; SILVER; UNCLASSIFIED DRUG; YNAMIDE DERIVATIVE;

EID: 84929648632     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2015.01.017     Document Type: Article
Times cited : (18)

References (56)
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    • For a recent study on Ficini [2+2] cycloadditions of ynamides with isoimidium salt, see
    • For a recent study on Ficini [2+2] cycloadditions of ynamides with isoimidium salt, see: Y. Yuan, L. Bai, J. Nan, J. Liu, and X. Luan Org. Lett. 16 2014 4316
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    • For a beautiful equivalent of this reaction using ynol-ethers and AgNTf2, see
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    • Synthesis of starting ynamides generally follows one of the following two approaches: 13,14
    • Synthesis of starting ynamides generally follows one of the following two approaches: 13,14
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    • For our recent work on [4+2] cycloadditions using 2-amidodienes, see
    • For our recent work on [4+2] cycloadditions using 2-amidodienes, see: L.-C. Fang, and R.P. Hsung Org. Lett. 2014 1826 16
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.