97485-97-7

Upstream product

• 58274-64-9 (E)-trimethyl((3-methylbuta-1,3-dien-1-yl)oxy)silane 
• 97467-30-6 5-hydroxy-2,2-diphenylnaphtho<1,2-d>-1,3-dioxole-6,9-dione 
• 107-86-8 3,3-dimethyl acrylaldehyde 
• 13379-22-1 2,5,8-trihydroxy-1,4-naphthoquinone 
• 2051-90-3 Dichlorodiphenylmethane 

Downstream Products

• 97467-33-9 6a,7,10,10a-tetrahydro-5,7-dihydroxy-9-methyl-2,2-diphenylanthra<1,2-d>-1,3-dioxole-6,11-dione 
• 97467-32-8 7,8,9,10-tetrahydro-5,7,8,9-tetrahydroxy-9-methyl-2,2-diphenylanthra<1,2-d>-1,3-dioxole-6,11-dione 
• 97485-98-8 (8R,9S)-5,8,9-Trihydroxy-9-methyl-2,2-diphenyl-7-trimethylsilanyloxy-7,8,9,10-tetrahydro-1,3-dioxa-cyclopenta[a]anthracene-6,11-dione 
• 139120-48-2 (1RS,2SR,3RS,4aRS,9aRS)-2,3-epoxy-1,5,6,8-tetrahydroxy-3-methyl-1,2,3,4,4a,9a-hexahydro-9,10-anthraquinone 5,6-benzophenone acetal 
• 139120-48-2 C₂₈H₂₂O₇ 
• 97467-33-9 (6aR,7S,10aR)-5,7-Dihydroxy-9-methyl-2,2-diphenyl-6a,7,10,10a-tetrahydro-1,3-dioxa-cyclopenta[a]anthracene-6,11-dione 

Relevant academic research and scientific papers

Pigments of Fungi. XXIII. Approaches Towards (+/-)Austrocortirubin from 3-Methyl-1-trimethylsilyloxybuta-1,3-diene

The products (5) and (21) of cycloaddition between 3-methyl-1-trimethylsilyloxybuta-1,3-diene (3) and naphthazarin (4), and between (3) and the naphthopurpurin acetal (2), respectively, are converted into the tetrahydroanthraquinones (16)-(18), (26) and (

Bostrycin: Structure Correction and Synthesis

The first synthesis of (+/-)-bostrycin (Scheme I), which is achieved with regio- and stereochemical control, is described.This synthesis, coupled with X-ray crystallographic and other studies, establishes that the structure of bostrycin is 2, which differ