252044-69-2

Upstream product

• 252044-67-0 L-mandeloyl-L-mandelic acid methyl ester 
• 252044-61-4 O^α-(9-fluorenylmethyloxycarbonyl)-L-mandelic acid 
• 155486-11-6 (S)-Phenyl-[(tetrahydro-pyran-2-yloxy)]-acetic acid methyl ester 
• 17199-29-0 (S)-Mandelic acid 
• 252044-68-1 O^α-(tetrahydropyran-2-yl)-L-mandeloyl-L-mandelic acid methyl ester 
• 252044-63-6 O^α-(tetrahydropyran-2-yl)-L-mandelic acid 
• 21210-43-5 (S)-Methyl mandelate 

Downstream Products

• 252044-71-6 L-mandeloyl-D-mandeloyl-L-mandelic acid methyl ester 
• 252044-72-7 L-mandeloyl-L-mandeloyl-L-mandelic acid methyl ester 

Relevant academic research and scientific papers

A general methodology for automated solid-phase synthesis of depsides and depsipeptides. Preparation of a valinomycin analogue

A general methodology is described that allows the solid-phase synthesis of depsides and depsipeptides from chiral α-hydroxy- and α-amino acids. The results of studies with different protecting groups for the α-hydroxy acids and coupling systems for depsi