Unusual reaction of allylic systems: homo- and cross-cyclizations leading to four-carbon rings

Tetrahedron

Volumn 65, Issue 11, 2009, Pages 2351-2355

  Siedlecka, Renata ^a  

^a WROCLAW UNIVERSITY OF TECHNOLOGY   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

(2,3 DIPHENYLCYCLOBUTYL)(PHENYL)METHYL ACETATE; (2,4 DIPHENYL CYCLOBUTANE 1,3 DIYL)BIS(PHENYLMETHANOL); 1,3 DIPHENYL 2,4 BIS [ALPHA ACETOXY BENZYL]CYCLOBUTANE; ALKENE; ALLYL COMPOUND; BRONSTED ACID; CARBON; CATION; CYCLOBUTANE; LEWIS ACID; LIGAND; PHENYL(2 PHENYL 4 (PROP 1 EN 2 YL)CYCLOBUTYL)METHYL ACETATE; PHENYL(2,3,4 TRIPHENYLCYCLOBUTYL)METHYL ACETATE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; CYCLIZATION; CYCLOADDITION; ELECTRON; PRIORITY JOURNAL; RACEMIZATION;

EID: 59749088942     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.01.016     Document Type: Article

References (25)

1. Namyslo J.C., and Kaufman D.E. Chem. Rev. 103 (2003) 1485-1537 and reference cited therein
2. Tanaka N., Okasaka M., Ishimaru Y., Takaishi Y., Sato M., Masato Okamoto M., Oshikawa T., Ahmed S.U., Consentino L.M., and Lee K.-H. Org. Lett. 7 (2005) 2997-2999
3. Doroth B., and Sulikowski G.A. Org. Lett. 8 (2006) 903-906
4. Lee-Ruff E. In: De Meijere A. (Ed). Methods of Organic Chemistry. Houben-Weyl Vol. E17e (1997), Georg Thieme Verlag, Stuttgart, Germany 141-148
5. Bach T. Synthesis (1998) 683-708
6. Lee-Ruff E., and Mladenova G. Chem. Rev. 103 (2003) 1449-1483 and reference cited therein
7. Thulasiram H.V., Erickson H.K., and Poulter C.D. Science 316 (2007) 73-76
8. Klein H., Freyberger G., and Mayr H. Angew. Chem., Int. Ed. Engl. 22 (1983) 49
9. Canales E., and Corey E.J. J. Am. Chem. Soc. 129 (2007) 12686-12687
10. Inanaga K., Takasu K., and Ihara M. J. Am. Chem. Soc. 126 (2004) 1352-1353
11. Takasu K., Ueno M., Inanaga K., and Ihara M. J. Org. Chem. 69 (2004) 517-521
12. Inanaga K., Takasu K., and Ihara M. J. Am. Chem. Soc. 127 (2005) 3668-3669
13. Takasu K., Hosokawa N., Inanaga K., and Ihara M. Tetrahedron Lett. 47 (2006) 6053-6056
14. Kniep C.S., Padias A.B., and Hall Jr. H.K. Tetrahedron 56 (2000) 4279-4288
15. Gassman P.G., Chavan S.P., and Fertel L.F. Tetrahedron Lett. 31 (1990) 6489-6492
16. Gassman P.G., and Lattes A.C. Tetrahedron Lett. 33 (1992) 157-160
17. Hojo M., Tomita K., Hirohara Y., and Hosomi A. Tetrahedron Lett. 34 (1993) 8123-8126
18. Knölker H.-J., Baum G., and Graf R. Angew. Chem., Int. Ed. Engl. 33 (1994) 1612-1615
19. Monti H., Audran G., Léandri G., and Monti J.-P. Tetrahedron Lett. 35 (1994) 3073-3076
20. Groaning M.D., Brengel G.P., and Meyers A.I. Tetrahedron 57 (2001) 2635-2642
21. Akiyama T., and Yamanaka M. Tetrahedron Lett. 39 (1998) 7885-7888
22. Staab H.A., and Kurmeier H.-A. Chem. Ber. 101 (1968) 2697-2708
23. Kabalka G.W., Dong G., and Venkataiah B. Org. Lett. 5 (2003) 893-896
24. Kowalczyk R., and Skarżewski J. Tetrahedron: Asymmetry 17 (2006) 1370-1379
25. Trost B.M., Belletire J.L., Godleski S., McDougal P.G., Balkovec J.M., Baldwin J.J., Christy M.E., Ponticello G.S., Varga S.L., and Springer J.P. J. Org. Chem. 51 (1986) 2370-2374