259136-26-0

Upstream product

• 75-66-1 2-methylpropan-2-thiol 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 

Downstream Products

• 1233480-07-3 tris(2-((tert-butylthio)methyl)phenyl)silane 
• 1383119-04-7 5,13-bis[(tert-butyldimethylsilyl)oxy]-9-{2-[(tert-butylsulfanyl)methyl]phenyl}-2,2-dimethyl-2-silatricyclo[8.4.0.0^{3,8}]tetradeca-1⁽¹⁰⁾,3⁽⁸⁾,4,6,11,13-hexaen-9-ol 
• 1333786-67-6 bis[2-(tert-butylthiomethyl)phenyl]silane 
• 1333786-80-3 bis[2-(tert-butylthiomethyl)phenyl]diiodosilane 
• 1333786-76-7 dibromobis[2-(tert-butylthiomethyl)phenyl]silane 
• 1333786-71-2 bis[2-(tert-butylthiomethyl)phenyl]dichlorosilane 
• 259136-28-2 2-(tert-butylthiomethyl)phosphinobenzene 
• 259136-27-1 (2-tert-butylsulfanylmethyl-phenyl)-phosphonic acid diethyl ester 

Relevant academic research and scientific papers

Synthesis and reactivities of dihydrosilanes tethered with two thioether moieties

Dihydrosilanes tethered with two thioether moieties, [2-(RSCH 2)C6H4]2SiH2(1a: R = t-Bu; 1b: R = i-Pr; 1c: R = Ph), were synthesized. Dihydrosilane 1b did not react with methanol, benzaldehyde, and ca

Synthesis and complexation of a new tripodal tetradentate ligand, a silyl ligand tethered with three thioether moieties

Iridium(III) and platinum(II) complexes with a new tripodal tetradentate ligand, tris[2-(tert-butylthiomethyl)-phenyl]silyl were synthesized. In addition, reaction of tris-(2-((tert-butylthio)methyl)phenyl)silane with [PdCl2(PhCN)2]

PROCESS FOR PRODUCING CYCLIC THIOETHER AND SYNTHETIC INTERMEDIATE THEREOF

The present invention provides a process for producing cyclic thioether compounds and their synthetic intermediates.[Means for Solution]A compound represented by general formula (5): [wherein G1: alkylene, R1: a thiol protecting grou

Highly Flexible Synthetic Routes to Functionalized Phospholanes from Carbohydrates

Highly functionalized phospholanes 15, 17, and 26 and the corresponding diastereomers in which the configurations of the phospholane carbon-2 and carbon-5 are inverted can be readily prepared from D-mannitol by displacement of the appropriate dimesylate or cyclic sulfate with dilithium-phosphide reagents. The diols from which these ligands are prepared can also be converted into diarylphosphinite ligands. A route to related monophosphines bearing hemilabile tert-butylthio groups is also described. Complexes of these ligands and of related deprotected derivatives are potentially useful for enantioselective catalysis in organic and aqueous media.