25090-79-3Relevant articles and documents
Efficient Syntheses of (+/-)-β-Cuparenone. Conjugate Addition of Organozinc Reagents
Greene, Andrew E.,lamsard, Jean-Philippe,Luche, Jean-Louis,Petrier, Christian
, p. 931 - 932 (1984)
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A short and efficient synthesis of (±)-β-cuparenone
Kulkarni, Mukund G.,Davawala, Saryu I.,Shinde, Mahadev P.,Dhondge, Attrimuni P.,Borhade, Ajit S.,Chavhan, Sanjay W.,Gaikwad, Dnyaneshwar D.
, p. 3027 - 3029 (2007/10/03)
A Wittig olefination-Claisen rearrangement strategy has been applied to achieve one of the shortest and efficient synthesis of (±)-β-cuparenone.
Total Synthesis of (+/-)-Cyclolaurene, (+/-)-Epicyclolaurene and (+/-)-β-Cuparenone
Srikrishna, Adusumilli,Krishnan, Kathiresan
, p. 3429 - 3436 (2007/10/02)
The first total synthesis of (+/-)-cyclolaurene (1) and (+/-)-epicyclolaurene (5), and a new route to (+/-)-β-cuparenone (4) are reported.Thus, orthoester Claisen rearrangement of the cinnamyl alcohol 8 furnished the ene-ester 10.Anhydrous CuSO4 catalysed