1226967-99-2

Upstream product

• 1226967-95-8 N-allyl-N-((2R,3S)-3-hydroxy-1-phenyl-5-(triethylsilyl)pent-4-yn-2-yl)-2-nitrobenzenesulfonamide 

Downstream Products

• 1226968-08-6 (2R,3S)-2-benzyl-1-(2-nitrophenylsulfonyl)-4-vinyl-1,2,3,6-tetrahydropyridin-3-ol 
• 1226968-05-3 (2R,3S,Z)-2-benzyl-4-methylene-1-(2-nitrophenylsulfonyl)-2,3,4,7-tetrahydro-1H-azepin-3-ol 
• 1226968-12-2 (2R,3S)-N-allyl-3-(2-nitrophenoxy)-1-phenylpent-4-yn-2-amine 
• 1226968-14-4 (3R,4S)-3-benzyl-4-ethynyl-2-prop-2-en-1-yl-3,4-dihydro-2H-5,1,2-benzoxathiazepine 1,1-dioxide 
• 1226968-03-1 (3S,4R)-4-(N-allyl-2-nitrophenylsulfonamido)-5-phenylpent-1-yn-3-yl acetate 

Relevant academic research and scientific papers

Stereochemical and skeletal diversity arising from amino propargylic alcohols

(Figure presented) An efficient synthetic pathway to the possible stereoisomers of skeletally diverse heterocyclic small molecules is presented. The change in shape brought about by different intramolecular cyclizations of diastereoisomeric amino propargy