Stereochemistry of nucleophilic substitution at the optically active trivalent phosphorus atom

Author(s):  
Jan Omelanczuk ◽  
Marian Mikołajczyk
1973 ◽  
Vol 28 (9-10) ◽  
pp. 620-624 ◽  
Author(s):  
J. Mikolajczyk ◽  
J. Michalski ◽  
A. Zwierzak

A series of esters of phosphorous-phosphoric anhydride containing cyclic ester groups at one or both phosphorus atoms were prepared. The typical biphilic character of these compounds has been found. Unexpectedly observed lack of reactivity of anhydrides containing cyclic ester groups at trivalent phosphorus atom with respect to diethylphosphoric and acetic acids is the starting point for discussion on the mechanism of acidolysis. Unusual inertness of PIII cyclic esters of phosphorous-phosphoric anhydride towards protic acids is discussed in terms of Hudson’s concept of steric retardation on quaternisation.


2004 ◽  
Vol 59 (8) ◽  
pp. 889-892
Author(s):  
Henri Brunner ◽  
Ilias Grau ◽  
Manfred Zabel

AbstractReaction of (η6-C6H5CH3)Mo(CO)3 with the easily accessible chiral chelate ligand P,P,Pʹ-tris- [(+)-9-phenyldeltacyclan-8-yl]-1,2-bis(phosphanyl)benzene P-P’ afforded the octahedral molybdenum carbonyl derivate (P-P’)Mo(CO)4 1 as a diastereomer mixture 1a (74%) and 1b (26%). Crystallization gave single crystals of (SP)-(P-P’)Mo(CO)4 1a. The X-ray structure analysis of compound 1a revealed the formation of an unusual triple-decker π-stack in the solid state.


Sign in / Sign up

Export Citation Format

Share Document