114495-36-2

Upstream product

• 75-36-5 acetyl chloride 

Downstream Products

• 112463-98-6 Acetic acid (3R,4S,5R)-4-hydroxy-5-(4-methoxy-benzyl)-2-oxo-pyrrolidin-3-yl ester 
• 112464-01-4 Acetic acid (3S,4R,5R)-4-hydroxy-5-(4-methoxy-benzyl)-2-oxo-pyrrolidin-3-yl ester 
• 112463-96-4 (1S,4R,5S)-4-(4-Methoxy-benzyl)-6-oxa-3-aza-bicyclo[3.1.0]hexan-2-one 
• 112463-97-5 (1R,4R,5R)-4-(4-Methoxy-benzyl)-6-oxa-3-aza-bicyclo[3.1.0]hexan-2-one 
• 112487-80-6 Acetic acid (3S,4R,5R)-4-methanesulfonyloxy-5-(4-methoxy-benzyl)-2-oxo-pyrrolidin-3-yl ester 
• 112463-93-1 (R)-2,2-Dichloro-3-hydroxy-4-methoxycarbonylamino-5-(4-methoxy-phenyl)-pentanoic acid methyl ester 
• 112463-94-2 (R)-3,3-Dichloro-4-hydroxy-5-(4-methoxy-benzyl)-pyrrolidin-2-one 
• 112463-95-3 (R)-3-Chloro-4-hydroxy-5-(4-methoxy-benzyl)-pyrrolidin-2-one 
• 27958-06-1 (2R,3S,4S)-3,4-dihydroxy-2-(4-methoxybenzyl)pyrrolidine 
• 112463-92-0 [(R)-1-Formyl-2-(4-methoxy-phenyl)-ethyl]-carbamic acid methyl ester 

Relevant academic research and scientific papers

Possible origin of electronic effects in Rh(I)-catalyzed enantioselective hydrogenation

(Chemical Equation Presented) Reducing the electron density of ligands switches the regioselectivity of Rh(I)-catalyzed hydrometalation. A reversal of the sense of chiral induction was also observed when chiral ligands are electronically tuned in the same