For 2-methylcyclohexan-1-one, the thermodynamic (more substituted) enolate is favoured by

1. Aany strong base at any temperature, since the ratio is always the same
2. BLDA in THF at $-78{}^{\circ }\mathrm{C}$ with short reaction time
3. CNaOEt in ethanol at $25{}^{\circ }\mathrm{C}$, where proton transfers equilibrate the enolates
4. DLDA in THF at $-78{}^{\circ }\mathrm{C}$ followed by immediate quench with $\mathrm{CH}{}_3\mathrm{I}$