122407-52-7

Upstream product

• 122347-08-4 2-{(1R,3R)-3-[(S)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-cyclopent-1-enylmethyl]-3-methyl-2-[1-trimethylsilanyloxy-meth-(Z)-ylidene]-cyclopentyl}-propionaldehyde 
• 120410-18-6 {(3S,4R,4aR,7S)-7-[(S)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-cyclopent-1-enylmethyl]-4,7-dimethyl-3,4,4a,5,6,7-hexahydro-cyclopenta[c]pyran-3-yloxy}-trimethyl-silane 
• 120410-12-0 {(3R,4R,4aR,7S)-7-[(S)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-cyclopent-1-enylmethyl]-4,7-dimethyl-3,4,4a,5,6,7-hexahydro-cyclopenta[c]pyran-3-yloxy}-trimethyl-silane 

Downstream Products

• 120410-13-1 (R)-2-{(1R,2R,3S)-3-[(S)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-cyclopent-1-enylmethyl]-2-hydroxymethyl-3-methyl-cyclopentyl}-propan-1-ol 
• 122347-02-8 2,2-Dimethyl-propionic acid (1R,2S,5R)-2-[(S)-5-((R)-2-benzyloxy-1-methyl-ethyl)-2-methyl-cyclopent-1-enylmethyl]-5-[(R)-2-(2,2-dimethyl-propionyloxy)-1-methyl-ethyl]-2-methyl-cyclopentylmethyl ester 
• 120354-78-1 2,2-Dimethyl-propionic acid (R)-2-[(1R,2R,3S)-3-[(S)-5-((R)-2-benzyloxy-1-methyl-ethyl)-2-methyl-cyclopent-1-enylmethyl]-2-(2-chloro-acetoxymethyl)-3-methyl-cyclopentyl]-propyl ester 
• 120354-77-0 2,2-Dimethyl-propionic acid (R)-2-{(1R,2R,3S)-3-[(S)-5-((R)-2-benzyloxy-1-methyl-ethyl)-2-methyl-cyclopent-1-enylmethyl]-2-hydroxymethyl-3-methyl-cyclopentyl}-propyl ester 
• 122347-09-5 2,2-Dimethyl-propionic acid (1R,2S,5R)-2-[(S)-5-((R)-2-benzyloxy-1-methyl-ethyl)-2-methyl-cyclopent-1-enylmethyl]-5-((R)-2-hydroxy-1-methyl-ethyl)-2-methyl-cyclopentylmethyl ester 
• 120354-88-3 Toluene-4-sulfonic acid (R)-2-((Z)-(3S,3aR,6aS,10aS)-6,9,10a-trimethyl-1,2,3,3a,4,6a,7,8,10,10a-decahydro-dicyclopenta[a,d]cycloocten-3-yl)-propyl ester 
• 24433-10-1 albolic acid 

Relevant academic research and scientific papers

Synthetic Photochemistry. Part 44. Total Synthesis of Ceroplastol II and Albolic Acid, 5-8-5-Membered Tricyclic Sesterterpenoid Insect Wax Constituents, via Stereocontrolled Silyloxy-Cope Rearrangement with a Normally Disfavoured Transition State

To a 1,5-diene, prepared by CrCl2-mediated condensation of two iridoid synthons, was appended a lactol moiety, which was subjected to a stereocontrolled silyloxy-Cope rearrangement to give, via a normally disfavoured boat transition geometry, a thermolysa