Intramolecular Diels-Alder cycloadditions of fulvenes. Application to the kigelinol, neoamphilectane, and kempane skeletons
BC Hong, FL Chen, SH Chen, JH Liao, GH Lee
Index: Hong, Bor-Cherng; Chen, Fon-Len; Chen, Shang-Hung; Liao, Ju-Hsiou; Lee, Gene-Hsiang Organic Letters, 2005 , vol. 7, # 4 p. 557 - 560
Full Text: HTML
Citation Number: 47
Abstract
A variety of polycyclic ring skeletons (eg, kigelinol, neoamphilectane, and kempene systems) can be prepared rapidly via intramolecular Diels-Alder cycloadditions (IMDA) of fulvenes. The length of the tethers and the diversity of the substituents on the fulvene core dictate the nature of the IMDA pathway.
Related Articles:
[Shindo, Mitsuru; Matsumoto, Kenji; Sato, Yusuke; Shishido, Kozo Organic Letters, 2001 , vol. 3, # 13 p. 2029 - 2030]
[Shindo, Mitsuru; Matsumoto, Kenji; Sato, Yusuke; Shishido, Kozo Organic Letters, 2001 , vol. 3, # 13 p. 2029 - 2030]
[Shindo, Mitsuru; Matsumoto, Kenji; Sato, Yusuke; Shishido, Kozo Organic Letters, 2001 , vol. 3, # 13 p. 2029 - 2030]
[Jones, Raymond C.F; Iley, James N.; Lory, Pedro M.J.; Coles, Simon C.; Light, Mark E.; Hursthouse, Michael B. Tetrahedron Letters, 2001 , vol. 42, # 23 p. 3951 - 3954]