73834-60-3

Upstream product

• 113531-09-2 2(S)-chloro-3-<(S)-α-methylbenzyl>-1,3,2-oxazaphophorinane 2-oxide 
• 111-42-2 2,2'-iminobis[ethanol] 

Downstream Products

• 58028-72-1 2(S)--3-<(S)-α-methylbenzyl>-1,3,2-oxazaphosphorinane 2-oxide 
• 60030-72-0 (R)-cyclophosphamide 

Relevant academic research and scientific papers

Asymmetric Synthesis of Enantiomeric Cyclophosphamides

An efficient asymmetric synthesis of the enantiomers of cyclophosphamide was developed on the basis of three importand steps: (1) a highly stereospecific synthesis of the 2-chloro-2-oxo-1,3,2-oxazaphosphorinane ring from an optically active amino alcohol