960507-06-6

Upstream product

• 13505-32-3 N-tosyl-(S)-phenylalanine 
• 63-91-2 L-phenylalanine 
• 98-59-9 p-toluenesulfonyl chloride 
• 1092547-35-7 (S)-N-allyl-N-(1-hydroxy-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide 

Downstream Products

• 1092547-40-4 (2S,3aR,4S,6aR,7aR)-cis-2-phenyl-4-benzyl-5-N-(p-methyl)-benzenesulfonyl perhydrothiazolo[3',4'-2,3]pyrrolo[4,5-c]pyrrole 
• 1092547-41-5 (2S,3aR,4S,6aR,7aR)-cis-2-(p-methyl)-phenyl-4-benzyl-5-N-(p-methyl)-benzenesulfonyl perhydrothiazolo[3',4'-2,3]pyrrolo[4,5-c]pyrrole 
• 1092547-42-6 (2S,3aR,4S,6aR,7aR)-cis-2-(p-methoxy)-phenyl-4-benzyl-5-N-(p-methyl)-benzenesulfonyl perhydrothiazolo[3',4'-2,3]pyrrolo[4,5-c]pyrrole 
• 1092547-43-7 (2S,3aR,4S,6aR,7aR)-cis-2-(p-chloro)-phenyl-4-benzyl-5-N-(p-methyl)-benzenesulfonyl perhydrothiazolo[3',4'-2,3]pyrrolo[4,5-c]pyrrole 
• 1092547-44-8 (2S,3aR,4S,6aR,7aR)-cis-2-(p-bromo)-phenyl-4-benzyl-5-N-(p-methyl)-benzenesulfonyl perhydrothiazolo[3',4'-2,3]pyrrolo[4,5-c]pyrrole 
• 1092547-45-9 (2S,3aR,4S,6aR,7aR)-cis-2-(p-fluoro)-phenyl-4-benzyl-5-N-(p-methyl)-benzenesulfonyl perhydrothiazolo[3',4'-2,3]pyrrolo[4,5-c]pyrrole 
• 949574-75-8 (3aR,6S,6aR)-cis-1-(4-chloro)phenyl-5-tosyl-6-benzyloctahydropyrrolo[3,4-b]pyrrole 
• 1092547-37-9 (3aR,6S,6aR)-cis-1-(4-methyl)phenyl-5-tosyl-6-benzyloctahydropyrrolo[3,4-b]pyrrole 
• 1092547-39-1 (3aR,6S,6aR)-cis-1-(4-fluoro)phenyl-5-tosyl-6-benzyloctahydropyrrolo[3,4-b]pyrrole 
• 1092547-38-0 (3aR,6S,6aR)-cis-1-(4-methoxy)phenyl-5-tosyl-6-benzyloctahydropyrrolo[3,4-b]pyrrole 
• 960520-66-5 (3aR,6S,6aR)-cis-1-(4-bromo)phenyl-5-tosyl-6-benzyloctahydropyrrolo[3,4-b]pyrrole 
• 1092547-36-8 (3aR,6S,6aR)-cis-1-phenyl-5-tosyl-6-benzyloctahydropyrrolo[3,4-b]pyrrole 

Relevant academic research and scientific papers

Aryl λ3-Iodane-Mediated 6-exo-trig Cyclization to Synthesize Highly Substituted Chiral Morpholines

A mild and efficient transition metal-free approach has been developed for the synthesis of highly substituted chiral morpholines from alkenols by amino acid-derived iodine(III) reagents via a 6-exo-trig cyclization. The key features of this work include

A novel diastereoselective 1,3-dipolar cycloaddition approach to cis-fused bispyrrolidines

The intramolecular cycloaddition reactions of non-stabilized azomethine ylides generated by the condensation of N-aryl glycines and an enantiopure N-allyl-tethered alkenyl aldehyde derived from (S)-phenyl alanine were investigated. The stereoselective reactions led to the formation of novel cis-fused enantiomerically pure octahydropyrrolo[3,4-b]pyrroles, and the strategy was expanded to the synthesis of enantiopure novel heterotricyclic skeletons, perhydrothiazolo[3′,4′-2,3]pyrrolo[4,5-c]pyrroles.