127477-63-8

Upstream product

• 64891-77-6 (2-13C)bromoacetic acid 
• 105-13-5 4-Methoxybenzyl alcohol 

Downstream Products

• 405282-71-5 [1,3-13C₂]-(E)-4-(4-bromo-benzyloxy)-1-(4-methoxy-benzyloxy)-but-2-ene 
• 405282-76-0 [2,4-13C₂]-(E)-4-(4-methoxy-benzyloxy)-but-2-enoic acid methyl ester 
• 405282-70-4 [2,4-13C₂]-(E)-4-(4-methoxy-benzyloxy)-but-2-en-1-ol 
• 405282-69-1 (4-methoxybenzyloxy)[2-13C]acetaldehyde 
• 127477-64-9 C₁₉⁽¹³⁾CH₂₁NO₅ 

Relevant academic research and scientific papers

Regioselective synthesis of 1,3,5-13 C3 and 2,4-13 C2-labeled 2-deoxyribonolactones

The synthesis of 1,3,5-13 C3- and 2,4-13 C2-labeled 5-0-bromobenzyl2-deoxyribonolactones 2, precursors to 13C-enriched nucleoside phosphoramidites for solid-phase synthesis of DNA oligonucletides, is

A mechanistic study of the FK-506 tricarbonyl system rearrangement: Synthesis of C.9 labeled FK-506

Hydroxide mediated benzilic acid rearrangement of a C.9-13C labeled FK-506 derivative gave 97% rearrangement thru a C.8→C.10 acyl shift mechanism.