157024-32-3Relevant articles and documents
Reactions of β-nitrostyrenes with stabilized nucleophiles
Yao, Ching-Fa,Yang, Cherng-Shi,Fang, Hui-Yu
, p. 6419 - 6420 (1997)
β-Nitrostyrenes 1 react with stabilized nucleophiles to generate hydroximoyl chloride 2 after workup with ice cold concentrated hydrochloric acid. One-pot synthesis of five-membered carbocycles or cyclic ethers from the Michael addition of the carbon nucl
Oxidative tandem alkoxide conjugate addition to nitroalkenes/radical 5-exo cyclizations - A versatile synthesis of functionalized 3-nitrotetrahydrofurans
Jahn, Ullrich,Rudakov, Dmytro,Jones, Peter G.
supporting information; experimental part, p. 1521 - 1539 (2012/02/17)
Structurally diverse functionalized 4-(1-haloalkyl)-3-nitrotetrahydrofurans were conveniently obtained in moderate to good yield and moderate to very good diastereoselectivity by an oxidative tandem process consisting of conjugate addition reaction of lit
One-pot synthesis of the hydroximoyl chlorides and [3.3.0] bicyclic compounds from the reactions of β-nitrostyrenes with stabilized nucleophiles
Kao, Kuo-Hsi,Yang, Cherng-Shi,Liu, Ju-Tsung,Lin, Wen-Wei,Fang, Hui-Yu,Yao, Ching-Fa,Chen, Kwunmin
, p. 13997 - 14014 (2007/10/03)
β-Nitrostyrenes 1 react with various stabilized nucleophiles to generate hydroximoyl chlorides and nitroalkanes after workup with ice cold concentrated hydrochloric acid. One-pot synthesis of bicyclic products from the Michael addition of different nucleophiles with β-nitrostyrenes 1 is reported.