87960-99-4Relevant academic research and scientific papers
Chlorination of 1,5-Anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol; Highly Stereoselective Preparation of α-D-Glucopyranosyl Chloride and ω-Chloroalkyl β-D-Glucopyranosides
Sakakibara, Tohru,Nomura, Yutaka,Yoshino, Kohji,Sudoh, Rokuro
, p. 449 - 450 (1983)
Chlorination of 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol in cyclic ethers such as tetrahydrofuran stereoselectively afforded the ω-chloroalkyl β-D-glucopyranoside derivatives, whereas in 1,4-dioxane α-D-glucopyranosyl chlor
