919110-89-7

Upstream product

• 558-13-4 carbon tetrabromide 
• 71350-63-5 (R)-2-benzyloxy-2-methylbutyraldehyde 
• 919110-88-6 (R)-2-Benzyloxy-2-methyl-butan-1-ol 
• 133562-44-4 (R)-2-Benzyloxy-2-methyl-butyric acid benzyl ester 

Downstream Products

• 919110-94-4 2-(1-benzyloxy-1-methyl-propyl)-11-hydroxy-5-methyl-1-oxa-benzo[a]anthracene-4,7,12-trione 
• 919110-81-9 2-((R)-4-Benzyloxy-4-methyl-hex-2-ynoyl)-1,8-dihydroxy-3-methyl-anthraquinone 
• 919110-93-3 8-Benzyloxy-2-((R)-4-benzyloxy-4-methyl-hex-2-ynoyl)-1-isopropoxy-3-methyl-anthraquinone 
• 919110-92-2 8-Benzyloxy-2-((R)-4-benzyloxy-1-hydroxy-4-methyl-hex-2-ynyl)-1-isopropoxy-3-methyl-anthraquinone 
• 919110-91-1 (R)-4-Benzyloxy-1-(8-benzyloxy-1-isopropoxy-9,10-dimethoxy-3-methyl-anthracen-2-yl)-4-methyl-hex-2-yn-1-ol 
• 919110-83-1 (R)-4-Benzyloxy-4-methyl-hex-2-ynal 

Relevant academic research and scientific papers

First enantioselective total synthesis and structure determination of the anthrapyran metabolite γ-indomycinone

(Diagram presented) The first total synthesis of (R)-γ-indomycinone has been achieved which allowed the determination of the configuration of the stereogenic center of natural γ-indomycinone as (S). The approach stands out for its generality and efficienc