141546-67-0

Upstream product

• 153899-35-5 Benzoic acid (2R,3R)-2-methoxy-3-methyl-4-oxo-butyl ester 
• 141546-66-9 1,6-di-O-benzoyl-3-deoxy-3-C-methyl-2-O-methyl-L-altritol 

Downstream Products

• 153899-36-6 (E)-(3S,4R)-4-Methoxy-6-(4-methoxy-phenyl)-3-methyl-hex-5-enal 
• 153899-38-8 (E)-(3S,4S)-2-[1-Hydroxy-meth-(E)-ylidene]-4-methoxy-6-(4-methoxy-phenyl)-3-methyl-hex-5-enoic acid methyl ester 
• 130640-32-3 (-)-oudemansin X 
• 141546-74-9 methyl (E)-(3S,4R)-4-methoxy-6-(4-methoxyphenyl)-3-methylhex-5-enoate 
• 153899-37-7 (E)-(3S,4R)-4-Methoxy-6-(4-methoxy-phenyl)-3-methyl-hex-5-enoic acid 
• 141546-69-2 (3S,4R)-5-benzyloxy-4-methoxy-3-methylpentanenitrile 
• 141546-73-8 (E)-(3S,4R)-4-methoxy-6-(4-methoxyphenyl)-3-methylhex-5-enenitrile 
• 141546-68-1 4-O-benzoyl-2-deoxy-1-O-methylsulfonyl-2-C-methyl-3-O-methyl-L-threitol 

Relevant academic research and scientific papers

Utilisation of L-Quebrachitol in Natural Product Synthesis. Total Synthesis and Absolute Configuration of (-)-Oudemansin X

The stereoselective conversion of the naturally occurring optically active cyclitol, L-quebrachitol 2, into antifungal β-methoxyacrylate, oudemansin X 1 is described.The first total synthesis of 1 fully confirmed the proposed absolute configuration of the

Total Synthesis of Antibiotic (-)-Oudemansin X Utilizing L-Quebrachitol as a Chiral Pool

The stereoselective conversion of naturally occurring optically active cyclitol, L-quebrachitol (2), into antifungal (E)-β-methoxyacrylate, oudemansin X is described.This synthesis fully confirmed the proposed absolute configuration of the antibiotic and