Abstract
Chiral biaryl alcohols were readily transformed in a single step, with chiral non-racemic 1,2-diamines, PCl3, and sulfur in CDCl3 - all in a NMR tube - to their diastereomeric diazaphospholidines and their diastereomeric ratios (also ee's) assessed directly.
| Original language | Undefined |
|---|---|
| Pages (from-to) | 5125-5128 |
| Number of pages | 4 |
| Journal | Tetrahedron letters |
| Volume | 0 |
| Issue number | 35 |
| DOIs | |
| Publication status | Published - 1992 |
Keywords
- IR-12332
- METIS-106610
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