100238-92-4Relevant academic research and scientific papers
A General Approach to the Synthesis of Butanolides: Synthesis of the Sex Pheromone of the Japanese Beetle
Baskaran, Sundarababu,Islam, Imadul,Chandrasekaran, Srinivasan
, p. 891 - 895 (2007/10/02)
A variety of substituted γ-hydroxy olefins 1 have been converted to butanolides 4 in very high yield in a three-step sequence involving bromoetherification, elimination, and oxidative cleavage.The key step in the overall transformation is the highly selective oxidative cleavage of enol ethers 3 with PCC under very mild reaction conditions.Application of this methodology has been exemplified in the synthesis of the Japanese beetle pheromone.
LEAD(IV) ACETATE-METAL HALIDE REAGENTS III. A NEW METHOD FOR THE SYNTHESIS OF TETRAHYDROFURAN, TETRAHYDROPYRAN AND LACTONE DERIVATIVES
Motohashi, Shigeyasu,Satomi, Masakichi,Fujimoto, Yasuo,Tatsuno, Takashi
, p. 2035 - 2039 (2007/10/02)
A new method for the synthesis of tetrahydrofuran, tetrahydropyran and lactone derivatives from γδ-, δε-unsaturated alcohols and βγ-, γδ-carboxylic acids is described.
