1254331-83-3

Upstream product

• 1254331-94-6 (S)-4-(4-methoxybenzyloxy)-2-(tert-butyldimethylsilyloxy)butanenitrile 
• 128461-65-4 3-(p-methoxybenzyloxy)propanal 
• 1254331-93-5 (S)-4-(4-methoxybenzyloxy)-2-hydroxybutanenitrile 

Downstream Products

• 1254331-84-4 (E,2S,6S)-8-(4-methoxybenzyloxy)-2,6-di(tert-butyldimethylsilyloxy)oct-4-enenitrile 
• 1254331-96-8 C₂₈H₅₀O₅Si₂ 
• 1254331-95-7 C₃₈H₇₀O₆Si₃ 
• 1254331-85-5 (2S,4E,6S,8E,10S)-12-(4-methoxybenzyloxy)-2,6,10-tri(tert-butyldimethylsilyloxy)dodeca-4,8-dienenitrile 
• 1254331-86-6 (2E,4S,6E,8S,10E,12S)-14-(4-methoxybenzyloxy)-4,4,12-tri(tert-butyldimethylsilyloxy)tetradeca-2,6,10-trienal 

Relevant academic research and scientific papers

Unified Strategy for 1,5,9- and 1,5,7-Triols via Configuration-Encoded 1,5-Polyol Synthesis: Preparation and Coupling of C15-C25 and C26-C40 Fragments of Tetrafibricin

Diverse classes of natural products contain chiral 1,5,9- and 1,5,7-triol stereotriads, including the novel fibrinogen receptor antagonist tetrafibricin. Biological activities associated with compounds containing these motifs warrant targeted synthetic st

Versatile configuration-encoded strategy for rapid synthesis of 1,5-polyol stereoisomers

The isolated stereogenic centers of 1,5-polyol-containing natural products present challenges to synthesis and structure determination. To address this problem, a configuration-encoded strategy defines each configuration within a simple 4-(arylsulfonyl)bu