ISSN:
0009-2940
Schlagwort(e):
Phosphanes, cyclopropenyl-
;
Phosphaalkenes, cyclopropenyl
;
Shifts, [1,3]-silyl and [1,3]-H
;
1-Aza-3-phosphaallenes
;
Cyclopropenyl substituents
;
Chemistry
;
Inorganic Chemistry
Quelle:
Wiley InterScience Backfile Collection 1832-2000
Thema:
Chemie und Pharmazie
Notizen:
Organophosphorus Compounds, 73[1]. - The Tri-tert-butyl-2-cyclopropen-1-yl Substituent as Kinetically Stabilizing Group for 1-Aza-3-phosphaallenes[2]The cyclopropenylphosphane 5 reacts with the isocyanates 6a-g to form the phosphaalkenes 7a-g. An analogous transformation occurs with the same phosphane and the bifunctional isocyanates 8a, b (→ 9a, b). In contrast, the reaction 5 + 6h ends at the stage of the tautomers 11h ⇆ 12h. Methanolysis of 7b and of 11h ⇆ 12h leads to the carbamoyl-cyclopropenylphosphanes 14a and b, respectively. Sodium hydroxide-catalyzed elimination of hexamethyldisiloxane from 7b, g and the tautomer mixture 11h ⇆ 12h yields the target 1-aza-3-phosphaallenes 16a-c.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1002/cber.19931261129
