76529-59-4

Upstream product

• 43125-15-1 3-phenyl-S-(2'-pyridyl) thiopropionate 
• 87420-26-6 (1R,2S,3R)-3-[N-Phenylsulfonyl-N-(3,5-dimethylphenyl)amino]bornan-2-ol 
• 79-03-8 propionyl chloride 

Downstream Products

• 108781-61-9 2-Hydroxy-2-methyl-3-phenyl-propionic acid (1R,2S,3R,4S)-3-[benzenesulfonyl-(3,5-dimethyl-phenyl)-amino]-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 98269-17-1 (2S,3S)-3-Hydroxy-2,4-dimethyl-pentanoic acid (1R,4S)-3-[benzenesulfonyl-(3,5-dimethyl-phenyl)-amino]-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 98269-17-1 (2S,3R)-3-Hydroxy-2,4-dimethyl-pentanoic acid (1R,4S)-3-[benzenesulfonyl-(3,5-dimethyl-phenyl)-amino]-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 98269-17-1 (2R,3S)-3-Hydroxy-2,4-dimethyl-pentanoic acid (1R,4S)-3-[benzenesulfonyl-(3,5-dimethyl-phenyl)-amino]-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 98269-17-1 (2R,3R)-3-Hydroxy-2,4-dimethyl-pentanoic acid (1R,4S)-3-[benzenesulfonyl-(3,5-dimethyl-phenyl)-amino]-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 98269-16-0 N-{(1R,2R,3S,4S)-3-[(E)-1-(tert-Butyl-dimethyl-silanyloxy)-propenyloxy]-4,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl}-N-(3,5-dimethyl-phenyl)-benzenesulfonamide 
• 108781-58-4 (S)-2-Hydroxy-propionic acid (1R,2S,3R,4S)-3-[benzenesulfonyl-(3,5-dimethyl-phenyl)-amino]-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 87420-17-5 (S)-2-Methyl-3-phenyl-propionic acid (1R,2S,3R,4S)-3-[benzenesulfonyl-(3,5-dimethyl-phenyl)-amino]-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 87420-18-6 (R)-2-Methyl-3-phenyl-propionic acid (1R,2S,3R,4S)-3-[benzenesulfonyl-(3,5-dimethyl-phenyl)-amino]-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 76582-38-2 (R)-2-Methyl-hexadecanoic acid (1R,2S,3R,4S)-3-[benzenesulfonyl-(3,5-dimethyl-phenyl)-amino]-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 76529-68-5 (S)-2-Methyl-hexadecanoic acid (1R,2S,3R,4S)-3-[benzenesulfonyl-(3,5-dimethyl-phenyl)-amino]-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 

Relevant academic research and scientific papers

STRUCTURE AND DIASTEREOSELECTIVITY OF THE α-HYDROXYLATION OF CHIRAL ESTER ENOLATES BY MOLYBDENUM PEROXO COMPLEX

Scope and limitations of the diastereoselective α-hydroxylation of chiral ester enolates by MoO5.Py.HMPT were investigated.An improved synthesis of natural (-)-verrucarinolactone ((-)-(2S,3R)-2-hydroxy-3-methyl-pentanolide) is described.