294190-37-7Relevant academic research and scientific papers
Michael reactions on conformationally flexible methyl 3-C-nitro-hex-2-enopyranoside derivatives
Sakakibara, Tohru,Tokuda, Kiohisa,Hayakawa, Tsutomu,Seta, Akinori
, p. 489 - 496 (2000)
Dimethyl malonate and dibenzoylmethane attacked the C-2 position of the title 3-nitro-2-enopyranosides from the side opposite the anomeric methoxyl group to afford the 3-enopyranosides (S(N)2' products). In the case of 2,4-pentanedione and ethyl acetoacet
