148338-52-7

Upstream product

• 74307-97-4 2-chloromethyl-4,4-dimethyl-4,5-dihydro-1,3-oxazole 
• 148338-51-6 (E)-(R)-2-[(2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-3-methyl-tetrahydro-pyran-2-yl]-pent-3-en-2-ol 
• 148354-88-5 (R)-2-[(2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-3-methyl-tetrahydro-pyran-2-yl]-pent-3-yn-2-ol 
• 148409-71-6 [(2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-3-methyl-tetrahydro-pyran-2-yl]-methanol 

Downstream Products

• 148354-89-6 (E)-(1S,2R)-4-[(2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-3-methyl-tetrahydro-pyran-2-yl]-1-(4,4-dimethyl-4,5-dihydro-oxazol-2-yl)-2-methyl-pent-3-en-1-ol 
• 148338-53-8 (E)-(R)-4-[(2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-3-methyl-tetrahydro-pyran-2-yl]-2-methyl-pent-3-en-1-ol 
• 148338-54-9 (2S,3R,4R)-4-[(2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-3-methyl-tetrahydro-pyran-2-yl]-2-methyl-pentane-1,3-diol 
• 148338-56-1 (2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-2-((E)-(S)-1,3-dimethyl-penta-1,4-dienyl)-3-methyl-tetrahydro-pyran 

Relevant academic research and scientific papers

Synthetic studies of the ionophore antibiotic zincophorin. 2. Iterative sigmatropic construction of the C1-C11 subunit

Advanced intermediates 22 and 23, representing the C1-C11 subunit of the ionophore zincophorin, have been prepared by a scheme incorporating sequential glycolate Claisen and [2,3] Wittig rearrangements to establish the key structural