Abstract
The ring opening of several dimethyl N-aziridinylphosphonates 3 with Cl2 and HCl was studied. The reaction was found to be stereospecific and in most cases regiospecific. Conformational preferences in these compounds could be correlated with 1,3 P-H (PNCCH) coupling constants and with reactivity in ring opening.
Original language | English |
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Pages (from-to) | 2273-2276 |
Number of pages | 4 |
Journal | Journal of Organic Chemistry |
Volume | 41 |
Issue number | 13 |
DOIs | |
State | Published - 1 Jun 1976 |
Externally published | Yes |