Erratum: An iron-catalysed chemo- and regioselective tetrahydrofuran synthesis (Chemical Communications (2005) (1996-1998) DOI: 10.1039/b501100k);An iron-catalysed chemo- and regioselective tetrahydrofuran synthesis

Chemical Communications

Volumn , Issue 15, 2005, Pages 1996-1998

  Hilt, Gerhard ^a   Bolze, Patrick ^a   Kieltsech, Iris ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ACRYLIC ACID DERIVATIVE; ALKADIENE; ALKENE DERIVATIVE; CALYXOLANE A; CALYXOLANE B; EPOXIDE; IRON; STYRENE DERIVATIVE; TETRAHYDROFURAN; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; DIASTEREOISOMER; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

EID: 18044397666     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b604110h     Document Type: Erratum

References (16)

1. For recent examples of the synthesis of tetrahydrofuran derivatives see: M. Nakamura, C. Liang and E. Nakamura. Org. Lett., 2004, 6, 2015; V. Nair, S. Mathai and R. L. Varma, J. Org. Chem., 2004, 69, 1413; C. Huo, X. Jia, W. Zhang, L. Yang, J. Lü and Z.-L. Liu, Synlett, 2004, 251; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem., 2004, 116, 1441; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem. Int. Ed., 2004, 43, 1417; R. Andrukiewicz, P. Cmoch, A. Gawel and K. Stalinski, J. Org. Chem., 2004, 69, 1844.
2. For recent examples of the synthesis of tetrahydrofuran derivatives see: M. Nakamura, C. Liang and E. Nakamura. Org. Lett., 2004, 6, 2015; V. Nair, S. Mathai and R. L. Varma, J. Org. Chem., 2004, 69, 1413; C. Huo, X. Jia, W. Zhang, L. Yang, J. Lü and Z.-L. Liu, Synlett, 2004, 251; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem., 2004, 116, 1441; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem. Int. Ed., 2004, 43, 1417; R. Andrukiewicz, P. Cmoch, A. Gawel and K. Stalinski, J. Org. Chem., 2004, 69, 1844.
3. For recent examples of the synthesis of tetrahydrofuran derivatives see: M. Nakamura, C. Liang and E. Nakamura. Org. Lett., 2004, 6, 2015; V. Nair, S. Mathai and R. L. Varma, J. Org. Chem., 2004, 69, 1413; C. Huo, X. Jia, W. Zhang, L. Yang, J. Lü and Z.-L. Liu, Synlett, 2004, 251; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem., 2004, 116, 1441; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem. Int. Ed., 2004, 43, 1417; R. Andrukiewicz, P. Cmoch, A. Gawel and K. Stalinski, J. Org. Chem., 2004, 69, 1844.
4. For recent examples of the synthesis of tetrahydrofuran derivatives see: M. Nakamura, C. Liang and E. Nakamura. Org. Lett., 2004, 6, 2015; V. Nair, S. Mathai and R. L. Varma, J. Org. Chem., 2004, 69, 1413; C. Huo, X. Jia, W. Zhang, L. Yang, J. Lü and Z.-L. Liu, Synlett, 2004, 251; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem., 2004, 116, 1441; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem. Int. Ed., 2004, 43, 1417; R. Andrukiewicz, P. Cmoch, A. Gawel and K. Stalinski, J. Org. Chem., 2004, 69, 1844.
5. For recent examples of the synthesis of tetrahydrofuran derivatives see: M. Nakamura, C. Liang and E. Nakamura. Org. Lett., 2004, 6, 2015; V. Nair, S. Mathai and R. L. Varma, J. Org. Chem., 2004, 69, 1413; C. Huo, X. Jia, W. Zhang, L. Yang, J. Lü and Z.-L. Liu, Synlett, 2004, 251; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem., 2004, 116, 1441; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem. Int. Ed., 2004, 43, 1417; R. Andrukiewicz, P. Cmoch, A. Gawel and K. Stalinski, J. Org. Chem., 2004, 69, 1844.
6. For recent examples of the synthesis of tetrahydrofuran derivatives see: M. Nakamura, C. Liang and E. Nakamura. Org. Lett., 2004, 6, 2015; V. Nair, S. Mathai and R. L. Varma, J. Org. Chem., 2004, 69, 1413; C. Huo, X. Jia, W. Zhang, L. Yang, J. Lü and Z.-L. Liu, Synlett, 2004, 251; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem., 2004, 116, 1441; T. K. Sarkar, S. A. Haque and A. Basak, Angew. Chem. Int. Ed., 2004, 43, 1417; R. Andrukiewicz, P. Cmoch, A. Gawel and K. Stalinski, J. Org. Chem., 2004, 69, 1844.
7. For a review on iron-catalysed reactions see: C. Bolm, J. Legros, J. Le Paih and L. Zotti, Chem. Rev., 2004, 104, 6217.
8. As NHC-ligand, precursor 1,3-bis(2,4,6-trimethylphenyl)-imidazolium chloride was used; A. J. Arduengo, III, R. Krafczyk, R. Schmutzler, H. A. Craig, J. R. Goerlich, W. J. Marshall and M. Unverzagt, Tetrahedron, 1999, 55, 14523.
9. For recent examples of the use of mixed ligand systems see: M. T. Reetz and X. G. Li, Tetrahedron, 2004, 60, 9709; M. T. Reetz, G. Mehler and A. Meiswinkel, Tetrahedron: Asymmetry, 2004, 15, 2165.
10. For recent examples of the use of mixed ligand systems see: M. T. Reetz and X. G. Li, Tetrahedron, 2004, 60, 9709; M. T. Reetz, G. Mehler and A. Meiswinkel, Tetrahedron: Asymmetry, 2004, 15, 2165.
11. J.-H. Kim and R. J. Kulawiec, J. Org. Chem., 1996, 61, 7656.
12. The relative stereochemistry of the products was determined a) by comparison with literature data for compound 6 in ref. 7; b) by NOESY spectra (of the diastereomeric mixtures).
13. Leading reference: A. Gansäuer, B. Rinker, N. Ndene-Schiffer, M. Pierobon, S. Grimme. M. Gerenkamp and C. Mück-Lichtenfeld, Eur: J. Org. Chem., 2004, 2337.
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16. As salene ligand, N,N-ethylenebis-(salicylidenimine) was used.