794567-06-9

Upstream product

• 63366-76-7 (toluene-4-sulfonylamino)acetic acid benzyl ester 
• 78-94-4 methyl vinyl ketone 
• 794567-08-1 (2R,3R)-(-)-3-hydroxy-3-methyl-1-(toluene-4-sulfonyl)pyrrolidine-2-carboxylic acid 
• 50487-71-3 4-methyl-N-(2-propenyl)benzenesulfonamide 
• 944413-16-5 4-methyl-N-(3-oxobutyl)-N-(2-oxoethyl)benzenesulfonamide 
• 944413-15-4 C₁₄H₂₁NO₅S 
• 944413-14-3 N-allyl-4-methyl-N-(3-oxobutyl)benzenesulfonamide 

Downstream Products

• 770743-83-4 (2S,3R)-(-)-3-hydroxy-3-methyl-1-(toluene-4-sulfonyl)pyrrolidine-2-carboxylic acid methyl ester 
• 681236-64-6 (2S,3R)-3-hydroxy-3-methylpyrrolidine-2-carboxylic acid 

Relevant academic research and scientific papers

Diastereo- and Enantioselective Synthesis of Bi- and Tricyclic N-Heterocycle-Fused β-Lactones

The utility of the nucleophile-catalyzed (Lewis base) aldol lactonization (NCAL) process for the diastereo- and enantioselective synthesis of N-heterocycle-fused-β-lactones from N-linked ketoacids is described. A series of bi- and tricyclic, N-heterocycle

Organocatalytic synthesis of (2S,3R)-3-hydroxy-3-methyl-proline (OHMePro), a component of polyoxypeptins, and relatives using OHMePro itself as a catalyst

An efficient synthesis of (2S,3R)-3-hydroxy-3-methylproline (OHMePro), a component of polyoxypeptins, and relatives was achieved, in which an intramolecular asymmetric aldol reaction of the ketoaldehyde using OHMePro itself as an organocatalyst constitute

A short-step synthesis of (2S,3R)-3-hydroxy-3-methylproline, a component of polyoxypeptins, using a tandem Michael-aldol reaction and optical resolution

A short-step synthesis of (2S,3R)-3-hydroxy-3-methylproline, a component of polyoxypeptins, using a tandem Michael-aldol reaction followed by its optical resolution using (-)-cinchonidine has been achieved.