284469-33-6Relevant academic research and scientific papers
Oxy-cope rearrangements of bicyclo[3.2.0]heptenones. Synthesis of bicyclo[4.2.1]non-l(4)-en-6-ones and bicyclo[5.2.1]dec-1(10)-en-5-ones
Verma, Sharad K.,Nguyen, Que H.,MacDougall, James M.,Fleischer, Everly B.,Moore, Harold W.
, p. 3379 - 3386 (2000)
6-exo-Methylbicyclo[3.2.0]hepten-7-ones and their 2-alkylidene analogues are readily prepared from dialkyl squarates. These compounds undergo facial oxy-Cope ring expansions upon treatment with vinyllithium; the former leads to bicyclo[4.2.1]non-1(4)-en-6
Oxy-Cope rearrangements of bicyclo[3.2.0]heptenones. Synthesis of bicyclo[4.2.1]non-1(4)-en-6-ones and bicyclo[5.2.1]dec-1(10)-en-5-ones
Verma, Sharad K.,Nguyen, Que H.,MacDougall, James M.,Fleischer, Everly B.,Moore, Harold W.
, p. 3379 - 3386 (2007/10/03)
6-exo-Methylbicyclo[3.2.0]hepten-7-ones and their 2-alkylidene analogues are readily prepared from dialkyl squarates. These compounds undergo facial oxy-Cope ring expansions upon treatment with vinyllithium; the former leads to bicyclo[4.2.1]non-1(4)-en-6
