82238-33-3

Upstream product

• 82238-25-3 trans-9-Phenylselenoxanthene-N-(benzenesulfonyl)selenilimine 
• 82238-25-3 cis-9-Phenylselenoxanthene-N-(benzenesulfonyl)selenilimine 
• 88048-85-5 phenyl[o-(phenylseleno)phenyl]methanol 
• 88048-84-4 2-formylphenyl phenyl selenide 
• 89-98-5 2-chloro-benzaldehyde 
• 23974-72-3 sodium phenylselenide 
• 82238-23-1 cis-9-Phenylselenoxanthene-N-(p-toluenesulfonyl)-selenilimine 
• 82238-23-1 trans-9-Phenylselenoxanthene-N-(p-toluenesulfonyl)selenilimine 

Downstream Products

• 52182-93-1 9-methoxy-9-phenylselenoxanthene 
• 30571-10-9 9-phenylselenoxanthenol 
• 85891-62-9 methyl 9-phenylselenoxanthen-9-ylpropiolate 
• 63857-17-0 methyl 3-oxopropionate 

Relevant academic research and scientific papers

CHEMISTRY OF CIS- AND TRANS-9-PHENYLSELENOXANTHENE-N-ARYLSULFONYLSELENILIMINES

cis- and trans-9-Phenylselenoxanthene-N-(arylsulfonyl)selenilimines were synthesized and isolated.Their stereochemistry was ascertained from the NMR spectra.Cis isomers reacted with chloramine-T or -B by an SN2 type substitution to form trans i

STEREOISOMERS OF SELENILIMINES: ISOLATION AND REACTIONS OF 9-PHENYLSELENOXANTHENE-N-ARYLSULFONYLSELENILIMINES

The isolated cis- and trans-9-phenylselenoxanthene-N-arylsulfonylselenilimines were not interconverted thermally. cis-Isomers were converted to trans-isomers by chloramine-T or -B in a fashion of SN2 type substitution. cis-Isomers did not rearrange but trans-isomers rearranged thermally to 9-arylsulfonamido-9-phenylselenoxanthenes, whereas both isomers underwent the base-catalyzed intermolecular rearrangement.