“…91 -92 It is of interest that the glycerophosphepan is a stable compound, while its analogues, containing chlorine, dialkylamino-groups, and other very simple substituents at the phosphorus atom, are very labile and readily oligomerise. 214 " 218 The last factor explains the low effectiveness of the synthesis of glycerophosphepans via an alternative scheme consisting in the phosphorylation of substituted glycerols by the chloro-and dialkylamino-phosphepans already mentioned. 91 ' 92 Glycerophospho(III)cyclanes are promising intermediates in the synthesis of different types of phospholipids.…”