99% Chirally selective synthesis via pinanediol boronic esters: insect pheromones, diols, and an amino alcohol
- 1 February 1986
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 108 (4) , 810-819
- https://doi.org/10.1021/ja00264a039
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Synthesis of Both the Enantiomers of Eldanolide (trans-3,7-Dimethyl-6-octen-4-olide), the Wing Gland Pheromone of the Male African Sugar-cane BorerAgricultural and Biological Chemistry, 1983
- Synthetic routes to 6,8-dioxabicyclo[3.2.1]octyl pheromones from D-glucose derivatives. 2. Synthesis of (+)-exo-brevicominThe Journal of Organic Chemistry, 1982
- A Stereoselective Synthesis of (±) Exobrevicomin; Synthetic Applications of Gamma-Alkoxy AllylboronatesSynthetic Communications, 1982
- Dominicalure 1 and 2: Components of aggregation pheromone from male lesser grain borerRhyzopertha dominica (F.) (Coleoptera: Bostrichidae)Journal of Chemical Ecology, 1981
- Stereoselective aldol condensations via boron enolatesJournal of the American Chemical Society, 1981
- Absolute configuration of (−)-4-methylheptan-3-ol, a pheromone of the smaller european elm bark beetle, as determined by the synthesis of its (3R,4R)-(+)- and (3S,4R)-(+)-isomersTetrahedron, 1977
- Brevicomin: Principal Sex Attractant in the Frass of the Female Western Pine BeetleScience, 1968