Synthesis of 3-halo-2,5-disubstituted furans via CuX mediated cyclization-halogenation reactions

Tetrahedron Letters

Volumn 52, Issue 12, 2011, Pages 1398-1400

  Yazici, Arife ^a   Pyne, Stephen G ^a  

^a UNIVERSITY OF WOLLONGONG   (Australia)

Author keywords

2,3,5 Trisubstituted furans; Cu(I) salts; Cyclization cyanation; Cyclization halogenation

Indexed keywords

2 PHENYLETHENYL 3 HYDROXYPYRROLIDINE; 3 HALO 2,5 DISUBSTITUTED FURAN DERIVATIVE; COPPER DERIVATIVE; FURAN DERIVATIVE; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CYCLIZATION; HALOGENATION; RING OPENING; SYNTHESIS;

EID: 79951774851     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.01.120     Document Type: Article

References (9)

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3. For the synthesis of substituted furans, see: (a) Marshall, J. A.; Robinson, E. D. J. Org. Chem. 1990, 55, 3450-3451;
4. (b) Hashmi, A. S. K. Angew. Chem., Int. Ed. Engl. 1995, 34, 1581-1583;
5. (c) Hashmi, A. S. K.; Lothar, S.; Ji-Hyun, C.; Frost, T. M. Angew. Chem., Int. Ed. 2000, 39, 2285-2288;
6. (d) Yao, T.; Zhang, X.; Larock, R. C. J. Am. Chem. Soc. 2004, 126, 11164-11165.
7. +.) 447.0331, found 447.0318.
8. +.) 447.0320, found 447.0331.
9. +) 441.2178, found 441.2180.