139219-84-4Relevant academic research and scientific papers
Metal-assisted fragmentation of N-aryl- and -alkyl-N-trimethylsilylaminosulfur chlorides and N-aryl- and -alkyl-aminosulfur chlorides in the presence of conjugated dienes: Synthesis and reactivity of 2-substituted-3,6-dihydro-1,2-thiazines
Bryce, Martin R.,Chesney, Antony,McKelvey, Graham N.,Batsanov, Andrei S.,Howard, Judith A. K.,Anderson, Martin
, p. 1825 - 1831 (2007/10/03)
N-Alkyl- and -aryl-N-trimethylsilylaminosulfur chlorides 2 and N-aryl- and -alkyl-aminosulfur chlorides 8 fragment in the presence of silver ions and a conjugated diene to yield 2-substituted-3,6-dihydro-1,2-thiarines 6 as the major products, possibly via
Alkylthionitroso and arylthionitroso compounds generated from N- trimethylsilyl-N-chlorothioalkylamine precursors
Bryce,Chesney,Heaton,McKelvey,Anderson
, p. 5275 - 5278 (2007/10/02)
A range of alkylthionitroso and arylthionitroso compounds have been generated by thermal fragmentation of N-trimethylsilyl-N- chlorothioalkyl(aryl)amine precursors, and intercepted by reaction with dimethylbutadiene to afford Diels-Alder and ene adducts.
Diels-Alder and Ene Reactions of New Transient Thionitrosoarenes (Ar-N=S) and Thionitrosoheteroarenes (Het-N=S) Generated from N-(Arylaminosulfanyl)- and N-(Heteroarylaminosulfanyl)-phthalimides: Synthesis of Cyclic and Acyclic Sulfenamides
Bryce, Martin R.,Heaton, Julie N.,Taylor, Paul C.,Anderson, Martin
, p. 1935 - 1944 (2007/10/02)
A series of new N-(arylaminosulfanyl)- and N-(heteroarylaminosulfanyl)-phthalimide derivatives 3i-m and 3o-r, has been prepared by reaction of chlorosulfanylphthalimide with the trimethylsilyl derivative of the appropriate arylamine or heteroarylamine.On
Generation and trapping of ortho-substituted thionitrosobenzenes: Competitive Diels-Alder and ene reactions with dimethylbutadiene
Bryce,Heaton
, p. 7459 - 7462 (2007/10/02)
Transient thionitrosoarenes, ArN=S, (2) that bear a substituent (CN, Br or Me) ortho to the reactive N=S group have been generated by two entirely different routes and intercepted with dimethylbutadiene to afford mixtures of Diels-Alder and ene adducts, (
