207223-30-1

Upstream product

• 207223-20-9 2S,5S,6R-2-ethyl-4,5-dimethyl-2-hydroxy-6-phenyl-morpholin-3-one 
• 762-72-1 allyl-trimethyl-silane 
• 78927-93-2 (5S,6R)-4,5-dimethyl-6-phenyl-morpholin-2,3-dione 

Downstream Products

• 916607-05-1 (5R,6R,8R,9S)-8-phenyl-5,9,10-trimethyl-1,3,7-trioxa-10-azaspiro[5.5]undecan-11-one 
• 916606-92-3 (2S,3S,5R,6S)-5-phenyl-2,6,7-trimethyl-1,4-dioxa-7-azaspiro[2,5]octan-8-one 
• 916607-06-2 (2S,3S_.6R)-2-allyl-2-((S)-1-(but-3-enyloxy)propan-2-yl)-4,5-dimethyl-6-phenylnorpholin-3-one 
• 916606-97-8 (2S,5S,6R)-2-((S)-1-(3-methylbut-3-enyloxy)ethyl)-2-hydroxy-4,5-dimethyl-6-phenylmorpholin-3-one 
• 916606-94-5 (2S,5S,6R)-2-allyl-2-((S)-1-(allyloxy)ethyl)-4,5-dimethyl-6-phenylmorpholin-3-one 
• 916606-99-0 (2S,5S,6R)-2-hydroxy-4,5-dimethyl-6-phenyl-2-((S)-1-(prop-2-ynyloxy)ethyl)morpholin-3-one 
• 916606-93-4 (2S,5S,6R)-2-allyl-2-((S)-1-hydroxyethyl)-4,5-dimethyl-6-phenylmorpholin-3-one 
• 916606-95-6 (2R,3S,6S,7S)-2-phenyl-3,4,7-trimethyl-1,8-dioxa-4-azaspiro[5.6]dodec-10-en-5-one 

Relevant academic research and scientific papers

Enantioselective synthesis of functionalized medium-sized oxacycles

(Diagram presented) Enantioselective routes to functionalized, seven-, eight-, and nine-membered oxacycles that are amenable to further elaboration have been developed. Salient features of the methodology include highly diastereoselective and regioselecti

Stereoselective synthesis of α-hydroxycyclopropanecarboxylic acids

Cyclopropanation of chiral α-alkoxy acrylamides derived from 1R,2S- ephedrine and α-keto acids provides cyclopropyl morpholinones with good diastereoselectivity. Removal of the ephedrine portion generates α- hydroxycyclopropane carboxamides which are read