927833-58-7Relevant academic research and scientific papers
Cyclopropyl methyl bromide-mediated gem-diallylation: Total synthesis of (±)-α-cuparenone
Shivakumar,Salunke, Ganesh B.,Kumar, Suneel
experimental part, p. 1952 - 1957 (2011/06/26)
The total synthesis of (±)-α-cuparenone, an aromatic sesquiterpene, has been described using the radical mediated gem-diallylation of substituted cyclopropyl methylbromide followed by ring-closing metathesis approach.
An efficient and practical total synthesis of (±)-α-cuparenone
Chavan, Subhash P.,Dhawane, Abasaheb N.,Kalkote, Uttam R.
, p. 3827 - 3830 (2008/09/17)
A one-pot cyclopentannulation approach as the key step for the total synthesis of (±)-α-cuparenone is described. Georg Thieme Verlag Stuttgart.
A facile total synthesis of (±)-α-cuparenone employing diallylation and RCM as key steps
Chavan, Subhash P.,Dhawane, Abasaheb N.,Kalkote, Uttam R.
, p. 965 - 966 (2008/02/04)
A short and concise total synthesis of α-cuparenone employing one-pot diallylation and RCM as the key steps is described.
