845536-34-7

Downstream Products

• 845536-31-4 (2S,4S,5S)-(5-methoxymethoxy-2,4-dimethyloct-7-ynyloxymethyl)benzene 
• 845536-38-1 (2S,4S,5S)-1-benzyloxy-5-methoxymethoxy-2,4-dimethyl-6-(2,4,5-trimethoxy-3-methylphenyl)hexane 
• 845536-37-0 (2S,3S,5S)-6-(6-benzyloxy-2-methoxymethoxy-3,5-dimethylhexyl)-3,4-dimethoxy-2-methylphenol 
• 845536-42-7 (2S,4S,5S)-2-(6-benzyloxy-2-methoxymethoxy-3,5-dimethylhexyl)-3,5,6-trimethoxy-4-methylbenzaldehyde 
• 845536-41-6 (2S,4S,5S)-1-benzyloxy-5-methoxymethoxy-2,4-dimethyl-6-(2,4,5-trimethoxy-3-methyl-6-bromophenyl)hexane 

Relevant academic research and scientific papers

Application of the Doetz reaction to construction of a major portion of the ansa macrocycle (-)-kendomycin

(Chemical Equation Presented) A Doetz reaction employing a terminal alkyne and a Fischer-type alkenylchromium carbenoid led to a pentasubstituted benzene from which a major portion of the Streptomyces metabolite (-)-kendomycin was synthesized.