Stereoselective synthesis of dominicalure 1 and 2: Components of aggregation pheromone from male lesser grain borerRhyzopertha dominica (F.)

[1]  W. Wadsworth Synthetic Applications of Phosphoryl‐Stabilized Anions , 2005 .

[2]  Lin Guo-qiang,et al.  Enantiomeric synthesis of dominicalure, aggregation pheromone of lesser grain borer,Rhyzopertha dominica (F.) , 1990, Journal of Chemical Ecology.

[3]  R. Silverstein,et al.  Dominicalure 1 and 2: Components of aggregation pheromone from male lesser grain borerRhyzopertha dominica (F.) (Coleoptera: Bostrichidae) , 1981, Journal of Chemical Ecology.

[4]  Romas J. Kazlauskas,et al.  (S)‐(−)‐ and (R)‐(+)‐1,1′‐Bi‐2‐Naphthol , 2003 .

[5]  Yoshinori Yamamoto,et al.  SELECTIVE REACTIONS USING ALLYLIC METALS , 1993 .

[6]  R. Rossi,et al.  Synthetic Applications of Alkyl E-2-Tributylstannyl-2-alkenoates: Selective Synthesis of (S)-1-Methylbutyl E-2-Methyl-2-pentenoate, an Aggregation Pheromone Component of Rhyzopertha dominica and Prostephanus truncatus. , 1993 .

[7]  R. Rossi,et al.  Selective Syntheses of (S)-1-Methylbutyl (E)-2,4-Dimethyl-2-Pentenoate, an Aggregation Pheromone Component of Rhyzopertha dominica, and of (E)-2-Butyl-2-Octenal, an Alarm Pheromone Component of Oecophylla longinoda via 2-Substituted 1-Sdlyl-1-Stannylethenes 1) , 1992 .

[8]  E. Dalcanale,et al.  Selective oxidation of aldehydes to carboxylic acids with sodium chlorite-hydrogen peroxide , 1986 .

[9]  R. Noyori,et al.  Asymmetric synthesis via axially dissymmetric molecules. 7. Synthetic applications of the enantioselective reduction by binaphthol-modified lithium aluminum hydride reagents , 1984 .

[10]  R. Noyori,et al.  Asymmetric synthesis via axially dissymmetric molecules. 6. Rational designing of efficient chiral reducing agents. Highly enantioselective reduction of aromatic ketones by binaphthol-modified lithium aluminum hydride reagents , 1984 .