77426-34-7Relevant articles and documents
REGIOSELECTIVE MONOALKYLATION OF 3-METHYL-1,2-CYCLOHEXANEDIONE
Utaka, Masanori,Hojo, Makoto,Takeda, Akira
, p. 445 - 448 (2007/10/02)
Monoalkylation of 3-methyl-1,2-cyclohexanedione was achieved regioselectively to give 6-alkyl-3-methyl-1,2-cyclohexanedione as a major product without the formation of O-alkylated or polyalkylated products.
THE DIOSPHENOL CLAISEN REARRANGEMENT
Ponaras, A. A.
, p. 4803 - 4806 (2007/10/02)
Thermal rearrangement of diosphenol allyl ethers provides a method for attachment of an allyl group to hindered carbon centers.