2-(Phenylsulfanyl)-1H-isoindole-1,3(2H)-dione
2-(Phenylsulfanyl)-1H-isoindole-1,3(2H)-dione structure
|
Common Name | 2-(Phenylsulfanyl)-1H-isoindole-1,3(2H)-dione | ||
|---|---|---|---|---|
| CAS Number | 14204-27-4 | Molecular Weight | 255.292 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 432.2±28.0 °C at 760 mmHg | |
| Molecular Formula | C14H9NO2S | Melting Point | 160-163ºC(lit.) | |
| MSDS | Chinese USA | Flash Point | 215.2±24.0 °C | |
|
Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles.
Org. Lett. 14(11) , 2726-9, (2012) Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles has been developed via cooperative catalysis of a chiral N,N'-dioxide-Sc(OTf)(3) complex and a Brønsted base. Utilizing readily available N-(phenylthio)phthalimide as the sulfur source,... |
|
|
Formation, characterization, and sub-50-nm patterning of organosilane monolayers with embedded disulfide bonds: An engineered self-assembled monolayer resist for electron-beam lithography. Wang X, et al.
Langmuir 19(23) , 9748-9758, (2003)
|
|
|
On the involvement of lipoic acid in. alpha.-keto acid dehydrogenase complexes. Rastetter WH, et al.
J. Am. Chem. Soc. 101(10) , 2752-2753, (1979)
|
|
|
Asymmetric phase-transfer reactions under base-free neutral conditions. Shirakawa S and Maruoka K.
Tetrahedron Lett. 55(29) , 3833-3839, (2014)
|
|
|
Direct, organocatalytic α-sulfenylation of aldehydes and ketones. Wang W, et al.
Tetrahedron Lett. 45(44) , 8229-8231, (2004)
|
|
|
The use of anhydrous CeCl3 as a catalyst for the synthesis of 3-sulfenyl indoles. Silveira CC, et al.
Tetrahedron Lett. 51(15) , 2014-2016, (2010)
|
|
|
Indium chloride: a versatile Lewis acid catalyst for the synthesis of 3-sulfenylindoles. Kumar PP, et al.
J. Sulfur Chem. 35(4) , 356-361, (2014)
|
|
|
A new facile sulfenylation of 2-acetylbenzimidazoles. Kumar PP, et al.
Phosphorus. Sulfur. Silicon Relat. Elem. 189(12) , 1775-1779, (2014)
|
|
|
Quaternized chitosan as an efficient catalyst for synthesis of N-alkylthio-phthalimides. Hu Z and Li S
Int. J. Chem. 2(2) , 213, (2010)
|
|
|
Efficient preparation of N-phenylsulfenyl ketimines from oximes or nitro compounds without racemization of alpha-stereocenters.
Org. Lett. 9(22) , 4635-4638, (2007) As N-sulfenyl imines (e.g., RR'C=N-SAr) can be readily transformed to their N-sulfinyl imines (RR'C=N-SOAr), N-sulfonyl imines (RR'C=N-SO2Ar), and N-sulfonyl oxaziridines, the very mild procedure developed to convert ketoximes and secondary nitro derivatives ... |