854374-69-9

Upstream product

• 157225-72-4 (S)-5-methyl-4-hexene-2-ol 
• 854374-57-5 5-(4-methoxy-benzyloxy)-2-methyl-hex-1-en-3-ol 
• 854374-58-6 (R)-2-ethylbut-3-enoic acid 

Downstream Products

• 854374-55-3 3-ethyl-6-[2-(4-methoxy-benzyloxy)-propyl]-5-methyl-3,6-dihydro-pyran-2-one 
• 854374-67-7 [2-ethyl-7-(4-methoxy-benzyloxy)-5-(3-methoxy-benzyloxy)-4-methyl-oct-3-enyloxy]triisopropylsilane 
• 854374-66-6 2-(4-methoxy-benzyloxy)-5-methyl-7-triisopropylsilanyloxymethyl-non-5-en-4-ol 
• 854374-68-8 4-(3-methoxy-benzyloxy)-5-methyl-7-triisopropylsilanyloxymethyl-non-5-en-2-ol 
• 854374-65-5 2-ethyl-7-(4-methoxy-benzyloxy)-4-methyl-oct-3-ene-1,5-diol 

Relevant academic research and scientific papers

Synthesis of the C12-C19 fragment of (+)-peloruside a through A diastereomer-discriminating RCM reaction

(Chemical Equation Presented) A short and efficient asymmetric synthesis of the C12-C19 fragment of the cytotoxic macrolide (+)-peloruside A has been achieved via a highly diastereomer-discriminating RCM of α-branched but-3-enoate ester of a methallylic a