299428-91-4

Upstream product

• 115404-48-3 (3S,4aR,8aS)-3-Benzyloxy-8-bromomethyl-4,4,7,8a-tetramethyl-1,2,3,4,4a,5,6,8a-octahydro-naphthalene 
• 115333-56-7 (4aR,6S,8aS)-(+)-3,4,4a,5,6,7,8,8a-octahydro-6-benzyloxy-1-hydroxymethyl-2,5,5,8a-tetramethylnaphthalene 
• 299428-90-3 3-((4aR,6S,8aS)-6-Benzyloxy-2,5,5,8a-tetramethyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-ylmethyl)-6-methyl-2,4-bis-(2-trimethylsilanyl-ethoxymethoxy)-benzoic acid ethyl ester 

Downstream Products

• 299428-93-6 ethyl (3S,4aR,6aR,12aR,12bS)-3-benzyloxy-1,2,3,4,4a,5,6,6a,12a,12b-decahydro-11-hydroxy-4,4,6a,9,12b-pentamethylbenz[a]xanthene-10-carboxylate 

Relevant academic research and scientific papers

Synthesis and Absolute Configuration of Hongoquercin B, a Sesquiterpene-substituted Orsellinic Acid Isolated as a Fungal Metabolite

(+)-Hongoquercin B (1), a weakly antibacterial fungal metabolite, was synthesized by starting from (S)-3-hydroxy-2,2-dimethylcyclohexanone, and its absolute configuration was determined as depicted by structure 1.