68036-35-1Relevant academic research and scientific papers
Transition-metal-free amination phosphoryl azide for the synthesis of phosphoramidates
Li, Qing,Sun, Xiaohua,Yang, Xiaoqin,Wu, Minghu,Sun, Shaofa,Chen, Xiuling
, p. 16040 - 16043 (2019/06/10)
A facile and efficient approach to phosphoramidates was developed via amination of phosphoryl azides. A variety of phosphoramidates were obtained in one step with good to excellent yields under a mild reaction system. The process uses easily available ami
Kinetics and mechanism of the benzylaminolysis of O,O-Diphenyl S-Aryl phosphorothioates in dimethyl sulfoxide
Adhikary, Keshab Kumar,Lee, Hai Whang
experimental part, p. 1625 - 1629 (2011/12/14)
Kinetic studies of the reactions of O,O-diphenyl Z-S-aryl phosphorothioates with X-benzylamines have been carried out in dimethyl sulfoxide at 55.0 °C. The Hammett (log k2 vs ?X) and Broensted [log k2 vs pKa(X)] plots for substituent X variations in the nucleophiles are biphasic concave downwards with a maximum point at X = H, and the unusual positive ρX and negative βX values are obtained for the strongly basic benzylamines. The sign of the cross-interaction constant (ρXZ) is negative for both the strongly and weakly basic nucleophiles. Greater magnitude of ρXZ value is observed with the weakly basic nucleophiles (ρXZ = -2.35) compared to with the strongly basic nucleophiles (ρXZ = -0.03). The deuterium kinetic isotope effects (kH/kD) involving deuterated benzylamines [XC6H4CH2ND2] are primary normal (kH/kD > 1). The proposed mechanism is a concerted SN2 involving a frontside nucleophilic attack with a hydrogen bonded, four-center-type transition state for both the strongly and weakly basic nucleophiles. The unusual positive ρX and negative βX values with the strongly basic benzylamines are rationalized by through-space interaction between the π-clouds of the electron-rich phenyl ring of benzylamine and the phenyl ring of the leaving group thiophenoxide.
Catalyst-free alkylation of sulfinic acids with sulfonamides via sp 3 C-N bond cleavage at room temperature
Liu, Cong-Rong,Li, Man-Bo,Cheng, Dao-Juan,Yang, Cui-Feng,Tian, Shi-Kai
supporting information; experimental part, p. 2543 - 2545 (2009/10/10)
An unprecedented catalyst-free alkylation of sulfinic acids with sulfonamides has been developed via sp3 C-N bond cleavage at room temperature. In the absence of external catalysts and additives, a wide variety of N-benzylic and N-allylic sulfonamides couple with sulfinic acids to give structurally diversified sulfones in moderate to excellent yields. Furthermore, the reaction of N-(2-acyl)allylic sulfonamides with sulfinic acids provides a convenient access to trisubstituted allyl sulfones with exclusive Z selectivity.
