| /paper/doi/10.1016/s0040-4039(00)01501-x | 0.000000 | 0.000000 |
| INIT | 0.000168 | 0.000168 |
| _initView | 0.000803 | 0.000971 |
| _initViewBasic | 0.000156 | 0.001127 |
| _initSiteModules | 0.000153 | 0.001280 |
| _initRouters | 0.000130 | 0.001410 |
| Sess + | 0.001211 | 0.002621 |
| Sess _ | 0.000094 | 0.002715 |
| pre dispatch _ | 0.000123 | 0.002838 |
| LC::doiAction START | 0.000277 | 0.003115 |
| LC::doiAction END to showListing | 0.163672 | 0.166787 |
| LC::showListing START | 0.000004 | 0.166791 |
| LC::showListing get reviews START | 0.000018 | 0.166809 |
| ES Review Search START | 0.000608 | 0.167417 |
| ES Review Search END | 0.006867 | 0.174284 |
| LC::showListing get reviews END | 0.000796 | 0.175080 |
| Done | 0.026762 | 0.201842 |
Good synthesis with comments for improvement
The article presents a synthetic methodology to prepare chiral N,N-disubstituted, 1,2-diamines, which can be convenient precursors to tridentate ligands.
Particularly, I used the synthetic route using cyclohexane-1,2-diamine (both racemic and enatiopure) to obtain a series,...