1269249-90-2

Upstream product

• 1269250-30-7 C₁₇H₂₆O₃ 
• 1269249-88-8 (1S,2R,5S)-1-ethoxycarbonyl-3,3,5-trimethyl-8-(propan-2-ylidene)bicyclo[3.3.0]octan-2-ol 

Downstream Products

• 1269249-92-4 (1S,5S,8R)-8-benzyloxy-1-ethoxycarbonyl-5,7,7-trimethyl-2-(2-hydroxyprop-2-yl)bicyclo[3.3.0]oct-2-ene 
• 1269249-95-7 (1S,5S,8R)-8-benzyloxy-1-ethoxycarbonyl-5,7,7-trimethyl-2-(propan-2-ylidene)bicyclo[3.3.0]oct-2-ene 
• 1269249-98-0 (1S,2R,5S,E)-2-benzyloxy-1-ethoxycarbonyl-3,3,5-trimethyl-8-[1-(phenylthio)propan-2-ylidene]bicyclo[ 3.3.0]octane 

Relevant academic research and scientific papers

Aliphatic C-H to C-C conversion: Synthesis of (-)-cameroonan-7α-ol

In the course of a synthesis of the tricyclic sesquiterpene (-)- cameroonan-7α-ol from the acyclic (〈)-citronellal, seven aliphatic C-H bonds were converted to C-C bonds, and three rings and four new stereogenic centers were established. 2011 American Chemical Society.