1222468-58-7

Upstream product

• 112520-09-9 2H-benzo[d][1,3]dithiole 1,1,3,3-tetraoxide 
• 104-55-2 3-phenyl-propenal 

Downstream Products

• 1203466-56-1 (S)-3-phenyl-3-(1,1,3,3-tetraoxo-2,3-dihydro-1H-1λ(6),3λ(6)-benzo[1,3]dithiol-2-yl)-propan-1-ol 
• 1203466-58-3 (S)-methyl 3-[(benzo[1,3]dithiole-1,1,3,3-tetraoxide)-2-yl]-3-phenylpropanoate 
• 1203466-57-2 (S)-3-[(benzo[1,3]dithiole-1,1,3,3-tetraoxide)-2-yl]-3-(phenyl)propanaldehyde dimethyl acetal 

Relevant academic research and scientific papers

1,3-Benzodithiole-1,1,3,3-tetraoxide (BDT) as a versatile methylation reagent in catalytic enantioselective Michael addition reaction with enals

A protocol of an organocatalytic highly enantioselective conjugate addition of nucleophilic BDT to enals has been developed and the versatile Michael adducts serve as useful building blocks for a variety of organic transformations.

Catalytic conjugate additions of geminal bis(sulfone)s: Expanding the chemistry of sulfones as simple alkyl anion equivalents

The value of cyclic gem-bis-(sulfone) 4 as a simple alkyl nucleophile equivalent in catalytic C-C bondforming reactions is demonstrated. The 1,4-type nucleophilic additions of bis-(sulfone) 4 to α,β-unsaturated ketones take place by assistance of catalyti