By Randolph P. Thummel
This sequence offers evaluation articles touching on molecular platforms that are of curiosity due essentially to the presence of structural good points or features approximately which past predictions could be in keeping with current wisdom of chemical thought.
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Extra resources for Advances in Theoretically Interesting Molecules (Volume 4: 1998)
1 Schltiter's Belt . . . . . . . . . . . . . . . . 2 Stops on the Road to a Tetrahexyl Cyclacene . . . . . . . 3 Beginnings of the Journey to a Tetrahexyl Cyclacene . . . . . 4 Off to a Tetrahexyl Cyclacene . . . . . . . . . . . Concluding Remarks . . . . . . . . . . . . . . . . References . . . . . . . . . . . . . . . . . . . Advances in Theoretically Interesting Molecules, Volume 4, pages 53-80 Copyright 9 1998 by JAI Press Inc.
J. Chem. -P. Heir. Chin Acta 1988, 71,544. 103. Tisler, M. Adv. Heterocycl. Chem. 1989, 45, 37. 104. Curtis, P. ; Grove, J. E Nature (London) 1947, 160, 574. 105. Grove, J. E; Hitchcock, P. B. J. Chem. , Perkin Trans. 1 1986, 1145. 106. Qureshi, A. ; Rickards, R. ; Kamal, A. Tetrahedron 1967, 23, 3801. 107. ; Wege, D. J. Chem. , Perkin Trans. 1 1989, 2089. 108. Sims, C. ; Wege, D. Aust. J. Chem. 1992, 45, 1983. 109. Cragg, G. ; Giles, R. G. E; Roos, G. H. P. J. Chem. , Perkin Trans. 1 1975, 1339; see also Fumagalli, S.
Attempts to introduce the final degree of unsaturation to deliver furo[3,4-b]furan (145) have been unsuccessful, although the formation in some of these reactions of dialdehyde 163, the product of hydration of 145, points to the intermediacy of 145. 88 Although the above route did not yield the parent furo[3,4-b]furan (145) and thieno[2,3-c]furan (149), several substituted derivatives of these ring systems have been prepared by other workers using a variety of non-cycloaddition approaches (Scheme 28).