Direct substitution of hydroxyl groups of allyl alcohols with alkyl groups by the reaction of lithium allyloxyalkylcuprates with N, N- …
Y Tanigawa, H Kanamaru, A Sonoda…
Index: Tanigawa,Y. et al. Journal of the American Chemical Society, 1977 , vol. 99, p. 2361 - 2363
Full Text: HTML
Citation Number: 38
Abstract
The allylic unit'is a common structural feature of many compounds of natural origin, and the most important synthon for such units are allyl alcohols. We wish now to report a novel and efficient method for direct substitution of a hydroxyl group of alcohols with alkyl or aryl groups of the corresponding or-ganolithium compounds in a single step as depicted in eq 1. The reaction appears to be general and particularly efficient for regio-and stereoselective ...
Related Articles:
Viscosity of associated liquids
[Panteleeva, Elena V.; Vaganova, Tamara A.; Shteingarts, Vitalij D.; Bilkis, Isaak I. Tetrahedron Letters, 1995 , vol. 36, # 46 p. 8465 - 8466]
Cyclopropanes from Allylic Chlorides via Hydroborination
[Hawthorne,M.F. Journal of the American Chemical Society, 1960 , vol. 82, p. 1886 - 1888]
Cyclopropanes from Allylic Chlorides via Hydroborination
[Hawthorne,M.F. Journal of the American Chemical Society, 1960 , vol. 82, p. 1886 - 1888]
[Hall,S.S. et al. Journal of Organic Chemistry, 1976 , vol. 41, # 9 p. 1494 - 1498]
The question of cyclic versus acyclic ions: The structure of [C10H12]+˙ gas phase ions
[Dass, Chhabil; Gross, Michael L. Organic Mass Spectrometry, 1985 , vol. 20, # 1 p. 34 - 40]