159465-83-5

Upstream product

• 3964-58-7 3-chloro-4-hydroxybenzoic acid 
• 100-39-0 benzyl bromide 

Downstream Products

• 106931-79-7 4-(benzyloxy)-3-chlorobenzoic acid 
• 184841-34-7 C₂₇H₃₅ClN₂O₈ 
• 1027604-35-8 C₂₀H₂₉ClN₂O₈ 
• 184841-33-6 (2S,3R)-2-Acetylamino-3-(4-benzyloxy-3-chloro-phenyl)-3-hydroxy-propionic acid methyl ester 
• 184841-30-3 2-Acetylamino-3-(4-benzyloxy-3-chloro-phenyl)-3-oxo-propionic acid methyl ester 
• 184841-32-5 3-(4-Benzyloxy-3-chloro-phenyl)-2-[(E)-hydroxyimino]-3-oxo-propionic acid methyl ester 
• 271800-14-7 (2S,3R)-2-Acetylamino-3-(3-chloro-4-hydroxy-phenyl)-3-hydroxy-propionic acid methyl ester 
• 184841-31-4 (S)-3-(4-Benzyloxy-3-chloro-phenyl)-3-hydroxy-propionic acid methyl ester 
• 184841-29-0 3-(4-Benzyloxy-3-chloro-phenyl)-3-oxo-propionic acid methyl ester 
• 123436-73-7 4-benzyloxy-3-chlorobenzoic acid chloride 
• 536974-86-4 4-benzyloxy-3-chloro-benzoic acid methyl ester 

Relevant academic research and scientific papers

Syntheses of the syn and anti α-amino-β-hydroxy acids of vancomycin: (2S, 3R) and (2R, 3R) p-chloro-3-hydroxytyrosines

Syntheses of (2S, 3R) and (2R, 3R) methyl p-chloro-3-hydroxytyrosinates 2 and 3 respectively, have been achieved from 3-chloro-4-hydroxybenzoic acid. These approaches relied on the asymmetric hydrogenation of highly functionalized carbonyl derivatives using chiral ruthenium complexes.

MULTICYCLIC COMPOUNDS AND METHODS OF USING SAME

The invention generally relates to compounds represented by Structural Formula I: or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of