The Journal of Organic Chemistry
Stereochemistry. LXIX. Ring opening of aziridine phosphonates. Correlation of structure, nuclear magnetic resonance spectra, and reactivity
A Hassner, JE Galle
Index: Hassner,A.; Galle,J.E. Journal of Organic Chemistry, 1976 , vol. 41, p. 2273 - 2276
Full Text: HTML
Citation Number: 5
Abstract
The ring opening of several dimethyl N-aziridinylphosphonates 3 with Clz and HC1 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 PH (PNCCH) coupling constants and with reactivity in ring opening.
Related Articles:
[Lebreton, Luc; Jost, Eric; Carboni, Bertrand; Annat, Jocelyne; Vaultier, Michel; Dutartre, Patrick; Renaut, Patrice Journal of Medicinal Chemistry, 1999 , vol. 42, # 23 p. 4749 - 4763]