By Randolph P. Thummel

This sequence provides evaluation articles relating molecular platforms that are of curiosity due basically to the presence of structural positive factors or features approximately which earlier predictions may be in line with current wisdom of chemical thought.

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3, Thummr R. , JAI Press, Greenwich, 1996, p. 37 and references therein. 80. Anthony, I. ; Wege, D. Tetrahedron Lett. 1987, 28, 4217. 81. Dimethyl fumarate was chosen as the dienophile because it yields each adduct (except in the case of 141) as a single stereoisomer. In the additions of annulated IBFs to maleic anhydride (Table 1 and Figure 1), k2 is the sum for endo and exo adduct formation. 82. Anthony, I. ; Wege, D. Aust. J. Chem. 1996, 49, 1263. 83. Wiersum, U. ; Eked, C. ; van der Plas, H.

B. PhD. Thesis, University of Western Australia, 1976. 40. Stringer, M. ; Wege, D. Tetrahedron Lett. 1980, 21, 3831. 41. Barton, J. W. in: Nonbenzenoid Aromatics, Vol. 1, Snyder, J. , Academic Press, New York, 1969, p. 50. 42. Palmer, M. ; Kennedy, S. M. F. J. Chem. , Perkin Trans. 1 1976, 81. 43. Garratt, P. ; Vollhardt, K. P. C. J. Am. Chem. Soc. 1972, 94, 7087. 44. Anthony, I. , unpublished results; Anthony, I. J. PhD. Thesis, University of Western Australia, 1988. 45. ; Sasaoka, M. J. Am. Chem.

H. J. Am. Chem. Soc. 1940, 62, 2038. 21. Cava, M. ; Mitchell, M. ; Deana A. A. J. Org Chem. 1960, 25, 1481. 22. ; Wege, D. Ausr J. Chem. 1988, 41,235. 23. ; Weinhold, P. Chem. Ber. 1962, 95, 1692. 24. ; Loubinoux, B. Bull. Soc. Chim. Fr. 1968, 3857. 25. Caub~re, P. Acc. Chem. Res. 1974, 7, 301. 26. Clar, E. The Aromatic Sextet; John Wiley, London, 1972. 27. ; Lloyd, D. J. Chem. Educ. 1986, 63, 306. 28. -C. J. Org. Chem. 1991, 56, 1858, and references therein. 29. Herndon, W. C. J. Org. Chem. 1975, 40, 3583.

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