ISSN:
1042-7163
Keywords:
Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
Six O, O-diethyl-N-acylphosphoramidates (1a-f) were synthesized. The reactions of their conjugate bases with haloalkanes were studied. The N/(phosphoryl)O/(carbonyl)O regioselectivity varied greatly, depending on the substrate, the haloalkane, the base, and other reaction conditions. The earlier [17] reaction of N-formyl substrate 1a that led to the N-phosphorylated formamidine was extended to other substrates 1. Again, the yields and the selectivity depended strongly on the structure of a substrate.
Additional Material:
4 Tab.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/hc.520040104
Permalink