831210-10-7

Upstream product

• 17199-29-0 (S)-Mandelic acid 
• 150058-64-3 (6-(((tert-butyldimethylsilyl)oxy)methyl)pyridin-2-yl)methanol 
• 831210-02-7 (2S,5S)-2-tert-butyl-5-[6-(tert-butyldimethylsilyloxymethyl)pyridin-2-ylmethyl]-5-phenyl[1,3]dioxolan-4-one 
• 831209-93-9 2-(bromomethyl)-6-((tert-butyldimethylsilyloxy)methyl)pyridine 
• 630-19-3 pivalaldehyde 
• 1195-59-1 2.6-bis(hydroxymethyl)pyridine 
• 831210-07-2 (2S,5S)-2-tert-butyl-5-(6-hydroxymethylpyridin-2-ylmethyl)-5-phenyl[1,3]dioxolan-4-one 

Downstream Products

• 831210-12-9 (2S,5S)-5-{6-[(N-allyl-N-phenylamino)methyl]pyridin-2-ylmethyl}-2-tert-butyl-5-phenyl[1,3]dioxolan-4-one 
• 1082553-07-8 (2S,5S)-2-tert-butyl-5-((6-((methyl(phenyl)amino)methyl)pyridin-2-yl)methyl)-5-phenyl-1,3-dioxolan-4-one 
• 1400278-22-9 C₁₄H₁₁NO₃ 
• 1400278-21-8 C₁₅H₁₃NO₄ 
• 1400278-19-4 C₂₂H₂₂N₂O 
• 1082553-06-7 (S)-3-{6-[(ethyl-phenylamino)-methyl]-pyridin-2-yl}-2-hydroxy-2-phenylpropionic acid 
• 1400278-18-3 (2S,5S)-2-tert-butyl-5-((6-((methyl( phenyl)amino)methyl)pyridin-2-yl)methyl)-5-phenyl-1,3-dioxolan-4-one 
• 1400278-13-8 (S)-2-hydroxy-3-(6-((methyl(phenyl)amino)methyl)pyridin-2-yl)-2-phenylpropanoic acid 
• 1400278-15-0 (S)-3-(6-((diphenylamino)methyl)pyridin-2-yl)-2-hydroxy-2-phenylpropanoic acid 
• 1400278-24-1 (2S,5S)-2-tert-butyl-5-((6-((diphenylamino)methyl)pyridin-2-yl)methyl)-5-phenyl-1,3-dioxolan-4-one 
• 1400278-14-9 (S)-3-(6-((tert-butyl(phenyl)amino)methyl)pyridin-2-yl)-2-hydroxy-2-phenylpropanoic acid 
• 1400278-23-0 (2S,5S)-2-tert-butyl-5-((6-((tert-butyl(phenyl)amino)methyl)pyridin-2-yl)methyl)-5-phenyl-1,3-dioxolan-4-one 
• 831210-15-2 thiolacetic acid S-(3-{[6-((2S,4S)-2-tert-butyl-5-oxo-4-phenyl[1,3]dioxolan-4-ylmethyl)pyridin-2-ylmethyl]phenylamino}propyl) ester 

Relevant academic research and scientific papers

cis-Dihydroxylation of alkenes by a non-heme iron enzyme mimic

Using the non-heme iron oxidase active site as a template, a peptidomimetic ligand has been designed, synthesized, and used to effect the dihydroxylation of alkene substrates. Fenton-type radical pathways are also observed. Georg Thieme Verlag Stuttgart.

Design and synthesis of an isopenicillin N synthase mimic

Towards the aim of creating a functional mimic of isopenicillin N synthase, a small molecule designed to coordinate around iron(II) and model the enzyme active site has been prepared in nine synthetic steps from 2,6- bis(hydroxymethyl)pyridine, (S)-(+)-ma