A convenient synthesis of new macrocyclic naphthalenophanes

Grützmacher H-F, Nolte G (1994)
Chemische Berichte 127(6): 1157-1162.

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Journal Article | Published | English
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The (1,4)naphthalenophanes 6a, 6b, 7a, and 7b were synthesized regiospecifically in two steps from the appropriate [alpha, beta]-di-1-naphthylalkanes by a Friedel-Crafts acetylation of the two naphthalene groups followed by cyclization/dimerization of the resulting diketones by a McMurray reaction. The macrocyclic naphthalenophanes 6a and 6b exist in solution as a mixture of conformers while 7a and 7b were identified as the anti isomers.
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Grützmacher H-F, Nolte G. A convenient synthesis of new macrocyclic naphthalenophanes. Chemische Berichte. 1994;127(6):1157-1162.
Grützmacher, H. - F., & Nolte, G. (1994). A convenient synthesis of new macrocyclic naphthalenophanes. Chemische Berichte, 127(6), 1157-1162.
Grützmacher, H. - F., and Nolte, G. (1994). A convenient synthesis of new macrocyclic naphthalenophanes. Chemische Berichte 127, 1157-1162.
Grützmacher, H.-F., & Nolte, G., 1994. A convenient synthesis of new macrocyclic naphthalenophanes. Chemische Berichte, 127(6), p 1157-1162.
H.-F. Grützmacher and G. Nolte, “A convenient synthesis of new macrocyclic naphthalenophanes”, Chemische Berichte, vol. 127, 1994, pp. 1157-1162.
Grützmacher, H.-F., Nolte, G.: A convenient synthesis of new macrocyclic naphthalenophanes. Chemische Berichte. 127, 1157-1162 (1994).
Grützmacher, Hans-Friedrich, and Nolte, Gerald. “A convenient synthesis of new macrocyclic naphthalenophanes”. Chemische Berichte 127.6 (1994): 1157-1162.
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