76897-39-7Relevant articles and documents
FACILE SYNTHESIS OF 3,4-DIHYDRO-4,4-DIMETHYL-2H-PYRAN-2-ONE VIA PALLADIUM CATALYZED TERMINAL OXIDATION OF 3,3-DIMETHYL-4-PENTENOATES
Tanaka, Mariko,Urata, Hisao,Fuchikami, Takamasa
, p. 3165 - 3168 (2007/10/02)
Selective terminal oxidation of 3,3-dimethyl-4-pentenoates does occur under chloride-free Wacker conditions in AcOH to give 5-acetoxy-3,3-dimethyl-4-pentenoates (7) and their analogues (2,8) in good yields.Successive cyclization of 7 and 8 at vapor phase pyrolysis on SiO2 affords 3,4-dihydro-4,4-dimethyl-2H-pyran-2-one (1).
Derivatives of 2H-pyran-2-one
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, (2008/06/13)
Processes for producing a (1α, 4α, 5α)-6,6-dimethyl-4-halo-substituted-methyl-3-oxabicyclo[3.1.0]hexan-2-one and its novel intermediates from known and inexpensive starting materials are described and exemplified.
Bicyclic lactone derivatives
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, (2008/06/13)
Novel intermediates for production of insecticidal cis-3-(2,2-disubstituted-ethenyl)-2,2-dimethylcyclopropanecarboxylates, processes for preparing the intermediates, and processes for preparing the final product insecticides via a novel bicyclic lactone intermediate are described and exemplified.