TY  - JOUR
AB  - 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.
DA  - 1994
DO  - 10.1002/cber.19941270629
KW  - Cyclophanes
KW  - McMurry reaction
KW  - naphthalenophanes
LA  - eng
IS  - 6
M2  - 1157
PY  - 1994
SN  - 0009-2940
SP  - 1157-1162
T2  - Chemische Berichte
TI  - A convenient synthesis of new macrocyclic naphthalenophanes
UR  - https://nbn-resolving.org/urn:nbn:de:0070-pub-17830941
Y2  - 2024-11-22T00:25:37
ER  -