Stereoselective allylation of chiral monoperoxyacetals
A Ahmed, PH Dussault
Index: Ahmed, Aqeel; Dussault, Patrick H. Tetrahedron, 2005 , vol. 61, # 19 p. 4657 - 4670
Full Text: HTML
Citation Number: 14
Abstract
Neighboring iodo-, alkoxy-, acetoxy-and silyl groups impart useful levels of diastereoselection in the Lewis acid-mediated allylation of monoperoxyacetals. Although monoperoxyacetals are found to be considerably less reactive than corresponding nonperoxidic acetals, similar stereochemical trends are observed in the two series.
Related Articles:
[Hojo; Sakuragi; Okabe; Hosomi Chemical Communications, 2001 , # 4 p. 357 - 358]
[Masuyama, Yoshiro; Suga, Takanori; Watabe, Akiko; Kurusu, Yasuhiko Tetrahedron Letters, 2003 , vol. 44, # 14 p. 2845 - 2847]
[Clayden, Jonathan; Julia, Marc Journal of the Chemical Society, Chemical Communications, 1994 , # 19 p. 2261 - 2262]