1579964-06-9

Upstream product

• 1579964-03-6 (E)-4-(2-(1,3-dithian-2-yl)phenoxy)but-2-en-1-ol 
• 1579964-02-5 (E)-((4-(2-(1,3-dithian-2-yl)phenoxy)but-2-en-1-yl)oxy)(tert-butyl)dimethylsilane 
• 6842-36-0 2-(2-hydroxyphenyl)-1,3-dithiane 
• 90-02-8 salicylaldehyde 

Downstream Products

• 1579964-07-0 (2E,4E)-6-(2-(1,3-dithian-2-yl)phenoxy)-1-(1H-pyrrol-1-yl)hexa-2,4-dien-1-one 
• 1579964-10-5 2-(((2E,4E)-6-oxo-6-(1H-pyrrol-1-yl)hexa-2,4-dien-1-yl)oxy)benzaldehyde 
• 1579964-11-6 diisopropyl ((1E,3E)-5-(2-formylphenoxy)penta-1,3-dien-1-yl)phosphonate 
• 1579964-12-7 (E)-dimethyl 2-(4-(2-formylphenoxy)but-2-en-1-ylidene)malonate 
• 1579964-08-1 diisopropyl ((1E,3E)-5-(2-(1,3-dithian-2-yl)phenoxy)penta-1,3-dien-1-yl)phosphonate 
• 1579964-14-9 (E)-dimethyl 2-(4-(2-(1,3-dithian-2-yl)phenoxy)but-2-en-1-ylidene)malonate 

Relevant academic research and scientific papers

Extending the stetter reaction with 1,6-acceptors

Pace Stetter: A new N-heterocyclic carbene (NHC)-catalysed transformation is described-the intramolecular vinylogous Stetter reaction. This transformation can be effected with both thiazolium and triazolium-based catalysts, using aromatic and aliphatic aldehydes, employing α,β,γ,δ- unsaturated esters, ketones, phosphonates and N-acylpyrroles, and can be conducted enantioselectively (see scheme). Copyright