919114-40-2

Upstream product

• 919114-39-9 3-(3-benzyloxy-2-methyl-butyryl)-4-isopropyl-oxazolidin-2-one 
• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 88635-99-8 (S)-3-((2S,3R)-3-Hydroxy-2-methyl-butyryl)-4-isopropyl-oxazolidin-2-one 
• 185300-90-7 (2R,3R)-3-Benzyloxy-2-methyl-butan-1-ol 

Downstream Products

• 919114-33-3 5-benzyloxy-4-methyl-hex-2-ynal 
• 919114-44-6 2-(2-benzyloxy-1-methyl-propyl)-11-isopropoxy-5-methyl-1-oxa-benzo[a]anthracene-4,7,12-trione 
• 919114-32-2 2-(5-benzyloxy-4-methyl-hex-2-ynoyl)-1-hydroxy-8-isopropoxy-3-methyl-anthraquinone 
• 919114-43-5 2-(5-benzyloxy-4-methyl-hex-2-ynoyl)-1,8-diisopropoxy-3-methyl-anthraquinone 
• 919114-42-4 2-(5-benzyloxy-1-hydroxy-4-methyl-hex-2-ynyl)-1,8-diisopropoxy-3-methyl-anthraquinone 
• 919114-41-3 5-benzyloxy-1-(1,8-diisopropoxy-9,10-dimethoxy-3-methyl-anthracen-2-yl)-4-methyl-hex-2-yn-1-ol 

Relevant academic research and scientific papers

Enantioselective total synthesis and structure determination of the antiherpetic anthrapyran antibiotic AH-1763 IIa

(Chemical Equation Presented) The antiherpetic anthrapyran antibiotic (14S,16R)-AH-1763 IIa (see right-hand structure) and its (14R,16R) diastereomer have been prepared in enantioselective total syntheses. The relative and absolute stereochemistry of the