144068-33-7

Upstream product

• 144401-98-9 2-(4-Methoxy-benzyloxy)-propionic acid ethyl ester 
• 824-94-2 p-methoxybenzyl chloride 
• 865620-61-7 methyl 2-(4-methoxybenzyloxy)propionate 

Downstream Products

• 865620-62-8 5-[2-(4-methoxy-benzyloxy)-propionylamino]-4-oxo-pentanoic acid methyl ester 
• 144068-34-8 2-(4-Methoxy-benzyloxy)-propionic acid (S)-1-{(S)-1-[(1R,3aR,4S,7aR)-4-(tert-butyl-dimethyl-silanyloxy)-7a-methyl-octahydro-inden-1-yl]-ethyl}-allyl ester 

Relevant academic research and scientific papers

Synthesis of the C6-C14 Fragment of Euphosalicin

The synthesis of the C6-C14 fragment of euphosalicin, a highly oxygenated modified jatrophane diterpene, is described. Key steps in the preparation of this versatile intermediate are an Ireland-Claisen rearrangement and a Shibasaki direct asymmetric aldol reaction.

Thiazole sulfonamide compounds for the treatment of neurodegenerative disorders

The present invention relates to compounds of the Formula: wherein R1 to R6, X, Z and A are as defined. These compounds have activity inhibiting production of Aβ-peptide. The invention also relates to pharmaceutical compositions and

A Practical Convergent Route to (23S,25R)-1α,25-Dihydroxyvitamin D3 26,23-Lactone

The Ireland-Claisen rearrangement of the lactate 8, prepared from the Inhoffen-Lythgoe diol 5, followed by iodolactonisation allowed easy access to the C-D-ring fragment 4, from which a novel convergent synthesis of (23S,25R)-1α,25-dihydroxyvitamin D