352463-56-0Relevant academic research and scientific papers
Solid-phase tandem radical addition-cyclization reaction: Triethylborane-induced reaction of oxime ethers anchored to polymer support
Miyabe, Hideto,Tanaka, Hirotaka,Naito, Takeaki
, p. 842 - 847 (2004)
Tandem radical addition-cyclization of oxime ethers anchored to polymer support was studied. The reaction of oxime ethers with stannyl radical proceeded effectively by the use of triethylborane as a radical initiator. The alkyl radical addition-cyclization reactions of oxime ether connected with α,β-unsaturated carbonyl group proceeded under iodine atom-transfer reaction conditions to give the functionalized azacycles via two carbon-carbon bonds-forming process.
Solid-phase tandem radical addition-cyclisation reaction of oxime ethers
Miyabe,Fujii,Tanaka,Naito
, p. 831 - 832 (2007/10/03)
The solid-phase tandem C-C bond-forming reactions of oxime ethers connected with α,β-unsaturated carbonyl groups proceeded effectively under iodine atom-transfer reaction conditions to give the azacycles or chiral oxacycles after cleavage of the resin.
