132439-87-3Relevant academic research and scientific papers
A Route to Functionalized Cyclic Ethers by Intramolecular Cycloaddition of Unsaturated Nitro Ethers
Hassner, Alfred,Dehaen, Wim
, p. 1181 - 1186 (2007/10/02)
A convenient conversion of aldehydes via nitroolefins 2 into cyclic ethers 6 fused to an isoxazoline ring involves formation of unsaturated nitroalkyl ethers 4 and subsequent intramolecular cycloaddition of an in situ-formed nitrile oxide olefin.The cyclization proceeds with stereoselective formation of trans over cis isomers in the tetrahydrofuran series and opposite stereoselectivity in the tetrahydropyran and hexahydrooxepine series, depending on the substituent R in the original nitro compound, thus providing access to stereoselectively functionalized cyclic ethers.
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.
