913066-81-6

Upstream product

• 1123216-48-7 C₃₁H₄₄O₆S 
• 1123216-46-5 C₁₆H₂₂O₄ 
• 50257-40-4 1-[(2,4,6-triisopropylphenyl)sulfonyl]-1H-imidazole 
• 913066-84-9 (E)-(3S,4R,5R)-4-Methyl-1-phenyl-octa-1,7-diene-3,5-diol 
• 913066-83-8 (E)-(2S,3S)-2-Methyl-5-phenyl-3-trimethylsilanyloxy-pent-4-enal 
• 913066-80-5 (2S,3R,4R,6R)-3-Methyl-6-(S)-oxiranyl-2-((E)-styryl)-tetrahydro-pyran-4-ol 
• 14371-10-9 (E)-3-phenylpropenal 
• 913066-79-2 Toluene-4-sulfonic acid (S)-2-hydroxy-2-[(2R,4R,5R,6S)-4-hydroxy-5-methyl-6-((E)-styryl)-tetrahydro-pyran-2-yl]-ethyl ester 

Downstream Products

• 1123216-49-8 C₁₆H₁₈O₃ 
• 1325710-75-5 C₄₂H₆₆O₈Si 
• 1325710-99-3 C₃₆H₅₂O₈ 
• 1325710-77-7 C₃₈H₅₆O₉ 
• 1325710-83-5 C₆₄H₁₀₂O₁₃Si 
• 1325710-84-6 C₁₈H₂₄O₄ 
• 1325710-85-7 C₄₅H₈₂O₈Si₃ 
• 1325711-09-8 C₃₉H₆₆O₈Si₂ 
• 1325710-86-8 C₅₀H₉₀O₉Si₃ 
• 1325711-10-1 C₃₂H₄₈O₉ 
• 1325711-11-2 C₃₅H₅₂O₉ 
• 1325711-12-3 C₄₁H₆₆O₉Si 
• 1325710-87-9 C₄₃H₇₀O₁₀Si 
• 1325710-92-6 C₂₁H₂₈O₄ 

Relevant academic research and scientific papers

An efficient, second-generation synthesis of the signature dioxabicyclo[3.2.1]octane core of (+)-sorangicin a and elaboration of the (Z,Z, E)-triene acid system

An efficient, second-generation synthesis of the signature dioxabicyclo[3.2.1]octane core of (+)-sorangicin A (1), in conjunction with an effective, stereocontrolled protocol to arrive at the requisite (Z,Z,E)-triene acid system has been developed. Highli

Synthesis of the C29-C37 bicyclic ether core of (+)-sorangicin A

(Chemical Equation Presented) Construction of the unique bicyclic bis-ether core of the macrolide (+)-sorangicin A has been achieved. This fragment was prepared by utilizing a one-pot cascade of three bond forming events. An epoxide opening of the epoxy tosylate 2 led to the formation of the tetrahydropyran and subsequently to a second epoxide. Finally, a second epoxide opening closed the tetrahydrofuran ring. The bicyclic fragment was synthesized in just nine steps from (E)-cinnamaldehyde.