79256-86-3

Upstream product

• 1089310-25-7 (2S,4S,5R)-2-ethoxy-3,4-dimethyl-5-phenyl-1,3,2-oxazaphospholidine-2-thione 
• 74-88-4 methyl iodide 

Downstream Products

• 79236-65-0 Acetic acid (1R,2S)-2-[((S)-ethoxy-methylsulfanyl-phosphoryl)-methyl-amino]-1-phenyl-propyl ester 
• 79236-67-2 (2S,4S,5R)-ethoxy-3,4-dimethyl-5-phenyl-1,3,2-oxazaphospholidin-2-one 
• 79236-67-2 (2R,4S,5R)-2-ethoxy-3,4-dimethyl-5-phenyl-1,3,2-oxazaphospholidine-2-one 
• 79236-66-1 (R)-Thiophosphoric acid O-ethyl ester S-methyl ester O'-((1R,2S)-2-methylamino-1-phenyl-propyl) ester; hydrochloride 

Relevant academic research and scientific papers

Stereochemictry of Alkaline Hydrolyses of 1,3,2-Oxazaphospholidine-2-thiones and Related Reactions

Essentially exclusive cleavage, with retention of configuration, of the endocyclic P-O bond occurs during basic hydrolysis of 2-alkoxy-1,3,2-oxazaphospholidine-2-thiones.In the 2-methyl analogues, P-O bond cleavage occurs with both inversion and retention