951008-01-8

Upstream product

• 878006-91-8 2-(4-benzyloxy-but-2-enyloxy) trimethyl 2-phosphonoacetate 
• 951008-02-9 C₂₄H₂₈O₄Se 
• 1580535-20-1 C₂₅H₃₂O₇SSe 
• 81028-03-7 (Z)-4-benzyloxy-but-2-en-1-ol 
• 100-39-0 benzyl bromide 

Downstream Products

• 951007-99-1 C₁₆H₂₀O₄ 
• 1239708-99-6 12,13-epi-ecklonialactone B 
• 121923-96-4 (-)-ecklonialactone B 
• 951008-07-4 C₁₆H₂₂O₂ 
• 951008-06-3 C₁₅H₁₈O₂ 
• 951008-05-2 C₁₅H₂₀O₃ 

Relevant academic research and scientific papers

The catalytic asymmetric claisen rearrangement (CAC) in natural product synthesis: Synthetic studies toward (-)-ecklonialactone B

A catalytic asymmetric Claisen rearrangement (CAC) in concert with a ring-closing metathesis (RCM) has been utilized in the enantioselective synthesis of the C10-C18 segment of ecklonialactone B. Georg Thieme Verlag Stuttgart.

Catalytic asymmetric claisen rearrangement of gosteli-type allyl vinyl ethers: Total synthesis of (-)-9,10-dihydroecklonialactone B

The enantioselective synthesis of (-)-9,10-dihydroecklonialactone B is described. The catalytic asymmetric Claisen rearrangement of a Gosteli-type allyl vinyl ether was utilized to afford an acyclic α-keto ester building block endowed with functionality a