78349-00-5

Upstream product

• 100-52-7 benzaldehyde 
• 6007-26-7 2-methyl-1,3-dithian 
• 27969-97-7 2-lithio-2-methyl-1,3-dithiane 

Downstream Products

• 90-63-1 (RS)-1-hydroxy-1-phenylpropan-2-one 
• 100-52-7 benzaldehyde 
• 72018-96-3 2-oxo-1,4-dithiacycloheptane 
• 4883-01-6 2-Benzoyl-2-methyl-1,3-dithiane 
• 247219-63-2 C₆S₂H₇OC₆H₅ 
• 247219-76-7 C₅S₂H₆C₆H₅C₃H₅O₂ 
• 247219-58-5 2-methyl-3-phenyl-5,6-dihydro-1,4-dithiepin 

Relevant academic research and scientific papers

Photooxidation of methyldithiepins into dithiepin carboxaldehydes in carbon tetrachloride

(equation presented) Methyldihydrodithiepins are converted into the corresponding carboxaldehydes via a simple and efficient oxidation by oxygen in carbon tetrachloride. The reaction is not a radical chain process. The proposed mechanism involves photoind

Enantioselective preparation of 2-substituted-1,3-dithiane 1-oxides using modified Sharpless sulphoxidation procedures

Enantioselective sulphoxidation of a wide range of 2-substituted-1,3-diathianes has been carried out using modified Sharpless conditions to furnish the corresponding sulphoxides in optically enriched form. Deacylation of 2-acyl-1,3-dithiane 1-oxide deriva

Selectivities in the Reactions of Alkyl-, Aryl- and Heterosubstituted Organotitanium Compounds

Solutions of the title compounds R-Ti(OR')3 (1) are generally available from organolithium (or magnesium) derivatives according to equation 1.It is shown (table 1) that some heterosubstituted organotitanium compounds are more stable thermally than their lithium counterparts.The reagents 1 are highly selective carbonylophiles (Tables 1 and 2), their reactivity can be modified by variation of the R'O-group (Table 3) and with the chiral (S)-2-methyl-1-butoxy group an enantioselective addition can be achieved.