127865-49-0Relevant academic research and scientific papers
Double diastereoselectivity in the intramolecular nitrile oxide-olefin cycloaddition (INOC) reaction
Kim, Hyoung Rae,Kim, Hyung Jin,Duffy, Jetty L.,Olmstead, Marilyn M.,Ruhlandt-Senge, Karin,Kurth, Mark J.
, p. 4259 - 4262 (2007/10/02)
An investigation of relative asymmetric induction and double diastereoselectivity in the intramolecular nitrile oxide-olefin cycloaddition (INOC) reaction is presented.
STEREOSELECTIVITY IN INTRAMOLECULAR 1,3-DIPOLAR CYCLOADDITIONS. NITRILE OXIDES VERSUS SILYL NITRONATES
Dehaen, W.,Hassner, A.
, p. 743 - 746 (2007/10/02)
Unlike nitrile oxides, silyl nitronates undergo highly stereoselective intramolecular cycloadditions to produce functionalized carbocyclic or heterocyclic rings.
A Two-Step Conversion of Carbonyl Compounds into Functionalized Five- and Six-Membered Ring Thioethers via Intramolecular Cycloaddition
Hassner, Alfred,Dehaen, Wim
, p. 5505 - 5510 (2007/10/02)
Reaction of aldehydes or ketones with nitromethane in the presence of unsaturated thiols led directly to unsaturated nitro sulfides 7, 12, 14, or 19.These compounds were converted by intramolecular nitrile oxide-olefin cycloaddition to tetrahydrothiopheno
