99% chirally selective synthesis via pinanediol boronic esters: insect pheromones, diols, and an amino alcohol
DS Matteson, KM Sadhu…
Index: Matteson,D.S.; Sadhu,K.M.; Peterson,M.L. Journal of the American Chemical Society, 1986 , vol. 108, p. 810
Full Text: HTML
Citation Number: 155
Abstract
Abstract: Chiral selectivities generally exceed 99% in the homologation of (+)-pinanediol alkylboronates (1) to (lS)-(1-chloroalky1) boronates (3) by reaction of 1 with (dichloromethy1) lithium at-100 OC followed by zinc chloride catalyzed rearrangement of the resulting borate complexes (2) at 0-25 OC. Diastereoselectivity falls to 95.7% with the methylboronate.(-)-Pinanediol leads to the 1R isomers. Nucleophilic displacements on (I- ...
Related Articles:
[Tsuchimoto; Joya; Shirakawa; Kawakami Synlett, 2000 , # 12 p. 1777 - 1778]
[Grieco, Liane M.; Halliday, Gary A.; Junk, Christopher P.; Lustig, Steven R.; Marshall, William J.; Petrov, Viacheslav A. Journal of Fluorine Chemistry, 2011 , vol. 132, # 12 p. 1198 - 1206]
[Grieco, Liane M.; Halliday, Gary A.; Junk, Christopher P.; Lustig, Steven R.; Marshall, William J.; Petrov, Viacheslav A. Journal of Fluorine Chemistry, 2011 , vol. 132, # 12 p. 1198 - 1206]
[Renson,M.; Beetz,J. Bulletin des Societes Chimiques Belges, 1961 , vol. 70, p. 537 - 548]
[Schultze, Peter; Wenclawiak, Bernd W. Organic Mass Spectrometry, 1989 , vol. 24, p. 235 - 240]