Endocyclic nucleophilic substitution at tetracoordinate sulfur (VI)
KK Andersen, S Chumpradit…
Index: Andersen, Kenneth K.; Chumpradit, Sumalee; McIntyre, Debra J. Journal of Organic Chemistry, 1988 , vol. 53, # 20 p. 4667 - 4675
Full Text: HTML
Citation Number: 12
Abstract
A search for endocyclic nucleophilic substitution at tetracoordinate sulfur (VI), usually sulfonyl sulfur, was carried out through the use of molecules so constructed that any intramolecular substitution process was forced to proceed through four-, five-, or six- membered cyclic transition states or intermediates with each ring incorporating both the nucleophile, sulfur atom, and leaving group. Three compounds [N-methyl-N-phenyl-4- ...
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]
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]
The Synthesis of Azaoxaspirane Steroid Alkaloids1
[Uhle,F.C. Journal of the American Chemical Society, 1961 , vol. 83, p. 1460 - 1472]