764583-34-8

Upstream product

• 98-80-6 phenylboronic acid 
• 764583-11-1 2-[(1E)-prop-1-en-1-ylsulfonyl]pyridine 
• 928768-94-9 (E)-2-((2-phenylprop-1-en-1-yl)sulfonyl)pyridine 
• 718615-25-9 diethyl [(pyridin-2-yl)sulfonyl]methylphosphonate 
• 2637-34-5 2-Sulfanylpyridine 
• 1003925-33-4 (Z)-1-[(2-pyridyl)sulfonyl]-1-propene 

Relevant academic research and scientific papers

Palladium-Catalyzed Remote ortho-C-H Alkenylation of Alkyl Aryl Sulfones: Access to Densely Functionalized Indane Derivatives

A practical method for the palladium-catalyzed ortho-olefination of benzyl and phenethyl 2-pyridyl sulfones with electron-deficient alkenes using N-fluoro-2,4,6-trimethylpyridinium triflate ([F+]) as the terminal oxidant is described. The chela

Enantioselective synthesis of chiral sulfones by Rh-catalyzed asymmetric addition of boronic acids to α,β-unsaturated 2-pyridyl sulfones

(Chemical Equation Presented) A general and efficient method for the rhodium-catalyzed enantioselective catalytic conjugate addition of organoboronic acids to α,β-unsaturated sulfones is described. The success of the process relies on the use of α,β-unsat

Catalytic asymmetric conjugate reduction of β,β-disubstituted α,β-unsaturated sulfones

(Chemical Equation Presented) Access to a chiral sulfone: Asymmetric conjugate reduction of β,β-disubstituted α,β-unsaturated 2-pyridylsulfones with silanes under CuI/binap catalysis provides chiral sulfones with excellent chemical yields and e

Rhodium-catalyzed enantioselective conjugate addition of organoboronic acids to α,β-unsaturated sulfones

(Chemical Equation Presented) A general method for the enantioselective catalytic conjugate addition to acyclic α,β-unsaturated sulfones is described. Using metal-chelating α,β-unsaturated pyridyl sulfones as substrates, the rhodium-catalyzed chiraphos-me