Mori, Kenji; Ikunaka, Masaya published the artcile< Pheromone synthesis. 65. Synthesis of all of the four energetically possible stereoisomers of 7-ethyl-2-methyl-1,6-dioxaspiro[4.5]decane. A pheromone produced by bees Paravespura vulgaris L. and Andrena haemorrhoa F>, Related Products of 617-55-0, the main research area is dioxaspirodecane ethylmethyl isomer preparation; pheromone ethymethyldioxaspirodecane isomer preparation.
All 4 energetically possible stereoisomers [(2R,5R,7R)-, (2R,5S,7S)-, (2S,5R,7R)- and (2S,5S,7S)] of 7-ethyl-2-methyl-1,6-dioxaspiro[4.5]decane were synthesized from Et (S)-lactate and di-Me (S)-malate or Me (R)-β-hydroxyvalerate employing dianion alkylation as the key-step.
Tetrahedron published new progress about Plant pheromones Role: SPN (Synthetic Preparation), PREP (Preparation). 617-55-0 belongs to class esters-buliding-blocks, and the molecular formula is C6H10O5, Related Products of 617-55-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics