40931-12-2

Upstream product

• 33524-31-1 2,5-dimethoxybenzyl alcohol 
• 495-08-9 gentisyl alcohol 
• 107-30-2 chloromethyl methyl ether 
• 2150-46-1 Methyl 2,5-dihydroxybenzoate 
• 40931-11-1 2,5-Bis-methoxymethoxy-benzoic acid methyl ester 

Downstream Products

• 179749-28-1 2-[(R)-2,6-Dimethyl-6-((E)-4-methyl-penta-1,3-dienyl)-cyclohex-1-enylmethyl]-benzene-1,4-diol 
• 1027932-86-0 2-[(R)-2,6-Dimethyl-6-((E)-4-methyl-penta-1,3-dienyl)-cyclohex-1-enylmethyl]-1,4-bis-methoxymethoxy-benzene 
• 179915-28-7 2-[(1S,2R,6R)-1-Hydroxy-2,6-dimethyl-2-((E)-4-methyl-penta-1,3-dienyl)-cyclohexylmethyl]-benzene-1,4-diol 
• 179915-27-6 2-[(1S,2R,6S)-1-Hydroxy-2,6-dimethyl-2-((E)-4-methyl-penta-1,3-dienyl)-cyclohexylmethyl]-benzene-1,4-diol 
• 179915-29-8 2-[(1R,2R,6R)-1-Hydroxy-2,6-dimethyl-2-((E)-4-methyl-penta-1,3-dienyl)-cyclohexylmethyl]-benzene-1,4-diol 
• 179749-23-6 2-[(1R,2R,6S)-1-Hydroxy-2,6-dimethyl-2-((E)-4-methyl-penta-1,3-dienyl)-cyclohexylmethyl]-benzene-1,4-diol 
• 179915-25-4 (1S,2R,6R)-1-(2,5-Bis-methoxymethoxy-benzyl)-2,6-dimethyl-2-((E)-4-methyl-penta-1,3-dienyl)-cyclohexanol 
• 179915-26-5 (1R,2R,6R)-1-(2,5-Bis-methoxymethoxy-benzyl)-2,6-dimethyl-2-((E)-4-methyl-penta-1,3-dienyl)-cyclohexanol 
• 40931-15-5 ethyl 2,5-dihydroxycinnamate 
• 40931-14-4 ethyl (E)-3-[2,5-bis(methoxymethoxy)phenyl]prop-2-enoate 
• 1227628-39-8 C₁₁H₁₅IO₄ 
• 179749-16-7 2-Chloromethyl-1,4-bis-methoxymethoxy-benzene 
• 13709-07-4 2,5-bis(methoxymethoxy)benzaldehyde 

Relevant academic research and scientific papers

A supple red alkone epirubicin than star-intermediates of the synthesis method (by machine translation)

The invention belongs to the field of medical synthesis, in particular relates to a supple red alkone epirubicin than star intermediate chemical synthesis method. The invention relates to 2, 5 - dihydroxy benzyl alcohol as the raw material synthetic suppl

Daunomycinone intermediate compound

The invention belongs to the field of medicine synthesis and particularly provides a daunomycinone intermediate compound. Daunomycinone can be purely chemically synthesized by adoption of the intermediate compound. By adoption of 2,5-dyhydroxylbenzyl alco

Daunomycinone intermediate compound

The invention belongs to the field of medicine synthesis and particularly provides a daunomycinone intermediate compound. Daunomycinone can be purely chemically synthesized by adoption of the intermediate compound. By adoption of 2,5-dyhydroxylbenzyl alco

Daunomycinone intermediate compound

The invention belongs to the field of medicine synthesis and particularly provides a daunomycinone intermediate compound. By adoption of 2,5-dyhydroxylbenzyl alcohol as a raw material for daunomycinone synthesis, low cost of raw materials, mild reaction c

Daunomycinone intermediate compound

The invention belongs to the field of medicine synthesis and particularly provides a daunomycinone intermediate compound. Daunomycinone can be purely chemically synthesized by adoption of the intermediate compound. By adoption of 2,5-dyhydroxylbenzyl alco

Daunomycinone intermediate compound

The invention belongs to the field of medicine synthesis and particularly provides a daunomycinone intermediate compound. Daunomycinone can be purely chemically synthesized by adoption of the intermediate compound. By adoption of 2,5-dyhydroxylbenzyl alco

Daunomycinone intermediate compound

The invention belongs to the field of medicine synthesis and particularly provides a daunomycinone intermediate compound. Daunomycinone can be purely chemically synthesized by adoption of the intermediate compound. By adoption of 2,5-dyhydroxylbenzyl alco

Total synthesis and absolute configuration of riccardiphenols A and B, isolated from the Liverwort Riccardia crassa

The title compounds were synthesized as optically active forms using chiral Michael addition of the imine, prepared from 2-methylcyclohexanone and (S)-(-)-phenylethylamine, to methyl propiolate. The etherification of the intermediate triol was accomplished by TsOH-catalyzed cyclization. The absolute configurations of the natural products, riccardiphenols A and B, were established as 1 and 2, respectively.