54882-03-0Relevant articles and documents
Application of TMSOTf in the Baylis-Hillman Adducts
Subramanian, Ravichandran
, p. 2345 - 2350 (2001)
A simple and convenient methodology for the stereoselective construction of 2-benzyl substituted trisubstituted olefins via TMSOTf catalyzed reaction of benzene with Baylis-Hillman adducts is described.
Reactivity of the 4-amino-5H-1,2-oxathiole-2,2-dioxide heterocyclic system: A combined experimental and theoretical study
De Castro, Sonia,Teresa Peromingo,Lozano, Angel E.,Camarasa, Maria-Jose,Velazquez, Sonsoles
supporting information; experimental part, p. 9620 - 9632 (2009/10/01)
The reactivity of the 4-amino-5H-1,2-oxathiole-2,2-dioxide (or β-amino-γ-sultone) heterocyclic system has scarcely been studied. Here we describe the reactivity of this system towards electrophiles and amines on readily available model substrates differently substituted at the C-5 position. A variety of C-electrophiles, carbonyl electrophiles (such as acyl chlorides, isocyanates, or aldehydes) and halogen or nitrogen electrophiles have been explored. Both the C-3 and 4-amino positions of the β-amino-γ- sultone system are able to undergo electrophilic reactions, and the reaction products depend on the electrophile used and on the reaction conditions. On the other hand, nucleophilic attack of amines occurs at the C-4 position of the β-amino-γ-sultone system only in spiranic substrates bearing alicyclic substituents at the C-5 position. A comparative computational study between spiranic and non-spiranic substrates suggests that conformational changes, undergone on intermediate compounds, account for the observed reactivity differences. Moreover, these conformational changes seem to bring about an increase of electron density on the N-4 and C-3 atoms of the enaminic system, and a possible enhancement in the reactivity of spiranic substrates towards electrophiles in the presence of amines. Experimental data consistent with this predicted enhanced reactivity is also presented.
