Corrigendum to "A highly diastereoselective approach to tetrahydrofurans via [3+2] cycloadditions of silylmethyl-substituted cyclopropanes with aldehydes and ketones". [Tetrahedron Lett. 47 (2006) 8043] (DOI:10.1016/j.tetlet.2006.09.064);A highly diastereoselective approach to tetrahydrofurans via [3+2] cycloadditions of silylmethyl-substituted cyclopropanes with aldehydes and ketones

Tetrahedron Letters

Volumn 47, Issue 46, 2006, Pages 8043-8047

  Gupta, Archana ^a   Yadav, Veejendra K ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY KANPUR   (India)

Author keywords

1,3 Dipole; 2,3,5 and 2,3,4,5 Substituted tetrahydrofurans; Cycloaddition

Indexed keywords

ALDEHYDE DERIVATIVE; CYCLOPROPANE DERIVATIVE; KETONE DERIVATIVE; TETRAHYDROFURAN DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CYCLOADDITION; STEREOCHEMISTRY; SYNTHESIS;

EID: 33749507354     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.10.091     Document Type: Erratum

References (39)

1. Alali F.Q., Liu X.-X., and McLaughlin J.L. J. Nat. Prod. 62 (1999) 504-540
2. Figadere B. Acc. Chem. Res. 28 (1995) 359-365
3. Zafra-Polo M.C., Figadere B., Gallardo T., Tormo J.R., and Cortes D. Phytochemistry 48 (1998) 1087-1117
4. Faul M.M., and Huff B.E. Chem Rev. 100 (2000) 2407-2473
5. In: Westley J.W. (Ed). Polyether Antibiotics: Naturally Occurring Acid Ionophores Vols. 1-2 (1982), Marcel Dekker, New York
6. Boivin T.L.B. Tetrahedron 43 (1987) 3309-3362
7. Ward R.S. Nat. Prod. Rep. 16 (1999) 75-96
8. Nicotra F. Top. Curr. Chem. 187 (1997) 55-83
9. Kang S.H., and Lee S.B. Tetrahedron Lett. 36 (1995) 4089-4092
10. Postema M.H.D. Tetrahedron 48 (1992) 8545-8599
11. Elliott M.C. J. Chem. Soc., Perkin Trans. 1 (2002) 2301-2323
12. Harmange J.-C., and Figadere B. Tetrahedron: Asymmetry 4 (1993) 1711-1754
13. Reissig H.-U., and Zimmer R. Chem. Rev. 103 (2003) 1151-1196
14. Yu M., and Pagenkopf B.L. Tetrahedron 61 (2005) 321-347
15. Yadav V.K., and Balamurugan R. Chem. Commun. (2002) 514-515
16. Yadav V.K., and Balamurugan R. Org. Lett. 5 (2003) 4281-4284
17. Yadav V.K., and Sriramurthy V. Angew. Chem., Int. Ed. 43 (2004) 2669-2671
18. Yadav V.K., and Vijaya Kumar N. J. Am. Chem. Soc. 126 (2004) 8652-8653
19. Yadav V.K., and Sriramurthy V. Org. Lett. 6 (2004) 4495-4498
20. Pohlhaus P.D., and Johnson J.S. J. Org. Chem. 70 (2005) 1057-1059
21. Pohlhaus P.D., and Johnson J.S. J. Am. Chem. Soc. 127 (2005) 16014-16015
22. Fleming I., and Sanderson P.E.J. Tetrahedron Lett. 28 (1987) 4229-4232
23. Knoelker H.-J., Jones P.G., and Wanzl G. Synlett (1998) 613-616
24. Smitrovitch J.H., and Woerpel K.A. J. Org. Chem. 61 (1996) 6044-6046
25. Liu D., and Kozmin S.A.. Org. Lett. 4 (2002) 3005-3007
26. Yadav V.K., and Sriramurthy V. J. Am. Chem. Soc. 127 (2005) 16366-16367
27. Yadav V.K., and Balamurugan R. Org. Lett. 3 (2001) 2717-2719
28. Sugita Y., Kawai K., and Yokoe I. Heterocycles 55 (2001) 135-144
29. Krapcho A.P. Synthesis (1982) 805-822
30. Zarbin P.H.G., Oliveira A.R.M., Simonelli F., Villar J.A.F.P., and Delay Jr. O. Tetrahedron Lett. 45 (2004) 7399-7400
31. Bernard A.M., Frongia A., Piras P.P., and Secci F. Org. Lett. 5 (2003) 2923-2926
32. Kobayashi S., Ueno M., Suzuki R., Ishitani H., Kim H.-S., and Wataya Y. J. Org. Chem. 64 (1999) 6833-6841
33. Taylor S.K., Atkinson R.F., Almli E.P., Carr M.D., Huis T.J.V., and Whittaker M.R. Tetrahedron: Asymmetry 6 (1995) 157-164
34. Lehmann J., and Pieper B. Tetrahedron: Asymmetry 3 (1992) 1537-1538
35. Figadere B., Harmange J.-C., Laurens A., and Cave A. Tetrahedron Lett. 32 (1991) 7539-7542
36. Ramaswamy S., and Oehlschlager A.C. Tetrahedron 47 (1991) 1145-1156
37. 2 (2 mL). The reaction was stirred at room temperature (30-32 °C) until the disappearance of 1a/1b/1c was confirmed by TLC. The reaction mixture was concentrated and the residue was chromatographed over silica gel (EtOAc/hexanes).
38. 2 (2 mL). The reaction was stirred at room temperature (30-32 °C) until the disappearance of 1 by TLC. The reaction mixture was concentrated and the residue was chromatographed over silica gel (EtOAc/hexanes).
39. 2Si: C, 74.51; H, 7.74%. Found: C, 74.40; H, 7.65%.