87118-43-2Relevant articles and documents
Pheromone Synthesis, CXXX. Synthesis of (4S,8S)- and (4S,8R)-4,8-Dimethyldecanal, the Stereoisomers of the Aggregation Pheromone of Tribolium castaneum
Mori, Kenji,Takikawa, Hirosato
, p. 497 - 500 (2007/10/02)
(4S,8S)- and (4S,8R)-4,8-Dimethyldecanal (1) were synthesized by starting from (R)-citronellic acid (2a), methyl (S)-3-hydroxyy-2-methylpropanoate (3a), and (S)-2-methyl-1-butanol (4a).
DIASTEREOTOPIC GROUP SELECTIVITY AT A PROSTEREOGENIC CARBON CENTER: SYNTHESIS OF (+/-)-SYN-4,8-DIMETHYLDECANAL
Schreiber, Stuart L.,Hulin, Bernard
, p. 4561 - 4564 (2007/10/02)
A group selective dealkylation reaction of a bridged ketal with trimethylsilyl iodide serves to control stereochemistry at carbon centers that are separated by five atoms.In combination with the iron/copper promoted fragmentation reaction of a hydroperoxi