reactions of sulfoxides bearing α-hydrogen(s) (RSOCHR1R2: R-alkyl or aryl; R1, R2 = H, alkyl, or aryl) with Grignardreagents (R3MgBr: R3 = Et, Ph, or vinyl) in the presence of the diisopropylaminomagnesium reagent, generated in situ by the treatment of diisopropylamine with the appropriate Grignardreagents in diethyl ether, have resulted in the formation of the corresponding sulfides (RSCR1R2R3) in moderate
Paris of diastereomeric sulphoximides and sulphilimines of known absolute configuration have been converted into the corresponding carbanions, which have a definite opticalstability.
已知绝对构型的非对映异构亚砜亚砜和亚砜亚胺的巴黎已经转化为具有确定的光学稳定性的相应碳负离子。
Alkylation with Oxalic Esters. Scope and mechanism
作者:Jan Bergman、Per-Ola Norrby、Peter Sand
DOI:10.1016/s0040-4020(01)87933-3
日期:1990.1
The Rearrangement of Alkyl Aryl Thioethers
作者:Wendell H. Taylor
DOI:10.1021/ja01303a506
日期:1936.12
Elimination Reactions. VII. A Comparison of Some Eliminations in Open-chain and Cyclic Systems