The Synthesis of Azaoxaspirane Steroid Alkaloids1
FC Uhle
Index: Uhle,F.C. Journal of the American Chemical Society, 1961 , vol. 83, p. 1460 - 1472
Full Text: HTML
Citation Number: 29
Abstract
Structural investigations in several laboratories culminated in provisional formulation of the natural products solasodine2 and toinatidine3 as ring F nitrogenous counterparts of the spiroketal sapogenins. The alkaloids merit close study both as members of the steroid family and as representatives of a mode of juncture not encountered elsewhere.
Related Articles:
ROMPGEL scavengers: A high-loading supported anhydride for sequestering amines and hydrazines
[Arnauld, Thomas; Barrett, Anthony G. M.; Cramp, Susan M.; Roberts, Richard S.; Zecri, Frederic J. Organic Letters, 2000 , vol. 2, # 17 p. 2663 - 2666]
[Mukaiyama, Teruaki; Aoki, Hidenori Chemistry Letters, 2005 , vol. 34, # 2 p. 142 - 143]
Novel reactivity of stabilized methylenetributylphosphorane: a new Mitsunobu reagent
[Tsunoda, Tetsuto; Ozaki, Fumie; Ito, Sho Tetrahedron Letters, 1994 , vol. 35, # 28 p. 5081 - 5082]
Endocyclic nucleophilic substitution at tetracoordinate sulfur (VI)
[Andersen, Kenneth K.; Chumpradit, Sumalee; McIntyre, Debra J. Journal of Organic Chemistry, 1988 , vol. 53, # 20 p. 4667 - 4675]
α, α, α-Trichloroketrylcahbonyl Compounds as Acylating Reagents of Amides
[Atanassova, I.A.; Petrov, J.S.; Ognjanova, V.H.; Mollov, N.M. Synthetic Communications, 1990 , vol. 20, # 14 p. 2083 - 2090]