The syntheses of 7,13‐dimethyl[3.2]metacyclophan‐10‐ene (5) and 7,10,11,13‐tetramethyl[3.2]metacyclophan‐10‐ene (6) starting from 1,3‐bis(4‐methylphenyl)propane (1) are reported. 5 exists in the anti conformation typical of [3.2]metacyclophan‐enes while 6 prefers the syn conformation because of steric repulsion between the methyl groups at the etheno bridge and at the aromatic rings.
No takes yet. Share an insight, caveat, or question.
Grützmacher et al. (1993) studied this question.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: