132155-41-0

Upstream product

• 94671-08-6 (6R,7S)-5-Oxo-7-(3,4,5-trimethoxy-phenyl)-6,7-dihydro-5H-indeno[5,6-d][1,3]dioxole-6-carboxylic acid methyl ester 
• 106-95-6 allyl bromide 
• 556-56-9 allyl iodid 

Downstream Products

• 132127-75-4 (5R,6R)-5,6-Diallyl-7-oxo-5-(3,4,5-trimethoxy-phenyl)-6,7-dihydro-5H-indeno[5,6-d][1,3]dioxole-6-carboxylic acid methyl ester 
• 132127-72-1 C₂₁H₂₀O₈ 
• 132127-72-1 C₂₁H₂₀O₈ 
• 132127-76-5 (5R,6S,7S)-5-Hydroxy-6-(2-hydroxy-ethyl)-7-(3,4,5-trimethoxy-phenyl)-6,7-dihydro-5H-indeno[5,6-d][1,3]dioxole-6-carboxylic acid methyl ester 
• 132127-69-6 (3aS,9S,9aS)-9-(3,4,5-Trimethoxy-phenyl)-1,2,3a,9-tetrahydro-3,5,7-trioxa-cyclopenta[a]-s-indacene-9a-carboxylic acid methyl ester 
• 132127-70-9 (3aS,9S,9aS)-9-(4-Hydroxy-3,5-dimethoxy-phenyl)-1,2,3a,9-tetrahydro-3,5,7-trioxa-cyclopenta[a]-s-indacene-9a-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Biomimetic Asymmetric Reduction of Tetrasubstituted Olefin 2,3-Disubstituted Inden-1-ones with Chiral and Regenerable NAD(P)H Model CYNAM

Because of the formidable development of the asymmetric reduction of tetrasubstituted olefins, an effective method is in urgent demand. Herein, through the biomimetic protocol of the coenzyme NAD(P)H, the reduction of tetrasubstituted olefin 2,3-substitut

Synthesis and Antitumor Activity of Structural Analogues of the Epipodophyllotoxins

Several ring-contracted analogues of the antitumor agent etoposide have been prepared.The synthesis of the simple indanyl system 3 is described along with two bicyclic systems of general structure 4 prepared through a stereoselective allylation of the ket