90381-86-5Relevant articles and documents
Chiral Sulfur Compounds. XXI. Addition of Azide Ion to β-Aryl-α-phenylsulfinylacrylates
Dong, Zemin,Hellmund, Kylie A.,Pyne, Stephen G.
, p. 1431 - 1436 (2007/10/02)
The reaction of methyl β-aryl-α-phenylsulfinylacrylates (1) with sodium azide/acetic acid gives triazoles (6) while the reaction of (1) with sodium azide/hydrochloric acid gives β-azido esters (7a, b).Reaction of (7a) with 1,8-diazabicycloundec-7-e
Selective Synthesis of α-Sulphenyl-, α-Sulphinyl-, and α-Sulphonyl-α,β-unsaturated Carbonyl Compounds by the Knoevenagel Reaction
Tanikaga, Rikuhei,Tamura, Tadashi,Nozaki, Yoshihito,Kaji, Aritsune
, p. 87 - 88 (2007/10/02)
Simple treatment of aldehydes with the carbonyl compounds (1) 2COCH2S(O)nAr; n = 0, 1, 2> and piperidine stereoselectively produces the condensation products (7), the stereochemistry of which is controlled by the steric requirements of two fu
