501369-28-4

Upstream product

• 89-82-7 pulegone 
• 74-88-4 methyl iodide 

Downstream Products

• 167073-63-4 Acetic acid (R)-2-[2-((1S,2S,3R)-1-hydroxy-2,3-dimethyl-cyclohexyl)-ethyl]-3-methyl-butyl ester 
• 166818-53-7 Acetic acid (S)-2-[2-((1S,2S,3R)-1-hydroxy-2,3-dimethyl-cyclohexyl)-ethyl]-3-methyl-butyl ester 
• 167073-62-3 (1S,2S,3R)-1-((R)-3-Isopropyl-pent-4-enyl)-2,3-dimethyl-cyclohexanol 
• 166818-51-5 (1S,2S,3R)-1-((S)-3-Isopropyl-pent-4-enyl)-2,3-dimethyl-cyclohexanol 
• 166818-52-6 (1S,2S,3R)-1-((S)-3-Hydroxymethyl-4-methyl-pentyl)-2,3-dimethyl-cyclohexanol 
• 501369-40-0 (2S,3S,6S,7R,8aR)-5-(3,4-Dimethoxy-benzyloxymethyl)-2-((E)-4-iodo-pent-3-enyl)-2,6,7-trimethyl-3-triethylsilanyloxy-6-vinyl-2,3,6,7,8,8a-hexahydro-chromen-4-one 
• 501369-25-1 [(3S,4R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-2-(3,4-dimethoxy-benzyloxymethyl)-3,4-dimethyl-3-vinyl-cyclohex-1-enyl]-[(2S,3R)-3-((E)-4-iodo-pent-3-enyl)-3-methyl-oxiranyl]-methanone 
• 501369-44-4 [(3S,4R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-2-(3,4-dimethoxy-benzyloxymethyl)-3,4-dimethyl-3-vinyl-cyclohex-1-enyl]-[(2R,3R)-3-((E)-4-iodo-pent-3-enyl)-3-methyl-oxiranyl]-methanol 
• 501369-26-2 (2S,3S,6S,7R,8aR)-5-(3,4-Dimethoxy-benzyloxymethyl)-3-hydroxy-2-((E)-4-iodo-pent-3-enyl)-2,6,7-trimethyl-6-vinyl-2,3,6,7,8,8a-hexahydro-chromen-4-one 
• 501369-39-7 [(3S,4R,6R)-2-(3,4-Dimethoxy-benzyloxymethyl)-6-hydroxy-3,4-dimethyl-3-vinyl-cyclohex-1-enyl]-[(2S,3R)-3-((E)-4-iodo-pent-3-enyl)-3-methyl-oxiranyl]-methanone 
• 501369-21-7 (1R,4S,5R)-[2-bromo-3-(3,4-dimethoxybenzyloxymethyl)-4,5-dimethyl-4-vinyl-cyclohex-2-enyloxy]-tert-butyldimethylsilane 
• 501369-20-6 (4S,5R)-2-bromo-3-(3,4-dimethoxybenzyloxymethyl)-4,5-dimethyl-4-vinyl-cyclohex-2-enone 
• 501369-35-3 (1S,4S,5R)-2-bromo-3-(3,4-dimethoxybenzyloxymethyl)-4,5-dimethyl-4-vinyl-cyclohex-2-enol 
• 501369-36-4 (1R,4S,5R)-2-bromo-3-(3,4-dimethoxybenzyloxymethyl)-4,5-dimethyl-4-vinyl-cyclohex-2-enol 

Relevant academic research and scientific papers

The first synthesis of ent-agelasine F

Agelasine F has previously been isolated from marine sponges (Agelas sp.) and has been associated with various bioactivities including inhibitory activity on Mycobacterium tuberculosis. No total synthesis of this natural product has been reported. ent-Age

Total synthesis of (+)-phomactin A using a B-alkyl Suzuki macrocyclization

A total synthesis of (+)-phomactin A is described using a B-alkyl Suzuki macrocyclization to incorporate the isolated trisubstituted olefin. This macrocyclization was accomplished with the sensitive hydrated furan ring in place. (R)-(+)-pulegone was used

Synthesis and the absolute configuration of the sesquiterpene aldehyde tridensenal from the Taiwanese liverwort Bazzania tridens

The absolute configuration of the sesquiterpene aldehyde tridensenal isolated from the Taiwanese liverwort Bazzania tridens has been determined by a total synthesis of the optically active compound as well as its diastereomer to have S,R configuration sta