59104-44-8

Upstream product

• 78-94-4 methyl vinyl ketone 
• 108-59-8 malonic acid dimethyl ester 

Downstream Products

• 151920-45-5 methyl 2-hydroxy-4-oxycyclohex-2-enecarboxylate 
• 1262290-88-9 C₁₈H₂₂O₇ 
• 1088991-72-3 2-methyl-6-(((3R,6R)-6-methyl-1-(2-(2H-1,2,3-triazol-2-yl)benzoyl)piperidin-3-yl)methoxy)pyridine 
• 1088994-00-6 (2-(2H-1.2.3-triazol-2-yl)phenyl )((2R,5R)-5-(hydroxymethyl)-2-methylpiperidin-1-yl)methanone 
• 1088993-98-9 ((3R,6R)-6-methylpiperidin-3-yl)-methanol 
• 128074-42-0 2-[(2Z,8E,10E)-6-Benzyloxymethyl-12-(tert-butyl-dimethyl-silanyloxy)-2-methoxymethoxy-3-methyl-dodeca-2,8,10-trienyl]-malonic acid dimethyl ester 
• 115349-76-3 2-[(2E,8E,10E)-6-Benzyloxymethyl-12-(tert-butyl-dimethyl-silanyloxy)-2-methoxymethoxy-3-methyl-dodeca-2,8,10-trienyl]-malonic acid dimethyl ester 
• 115368-96-2 2-((2Z,8E,10E)-6-Benzyloxymethyl-12-hydroxy-2-methoxymethoxy-3-methyl-dodeca-2,8,10-trienyl)-malonic acid dimethyl ester 
• 128074-43-1 2-((2E,8E,10E)-6-Benzyloxymethyl-12-hydroxy-2-methoxymethoxy-3-methyl-dodeca-2,8,10-trienyl)-malonic acid dimethyl ester 
• 115349-75-2 ((2E,4E,10E)-7-Benzyloxymethyl-12-chloro-11-methoxymethoxy-10-methyl-dodeca-2,4,10-trienyloxy)-tert-butyl-dimethyl-silane 
• 128074-41-9 ((2E,4E,10Z)-7-Benzyloxymethyl-12-chloro-11-methoxymethoxy-10-methyl-dodeca-2,4,10-trienyloxy)-tert-butyl-dimethyl-silane 
• 115349-74-1 (2E,8E,10E)-6-Benzyloxymethyl-12-(tert-butyl-dimethyl-silanyloxy)-2-methoxymethoxy-3-methyl-dodeca-2,8,10-trien-1-ol 
• 115349-73-0 (2Z,8E,10E)-6-Benzyloxymethyl-12-(tert-butyl-dimethyl-silanyloxy)-2-methoxymethoxy-3-methyl-dodeca-2,8,10-trien-1-ol 
• 115349-71-8 (2E,8E,10E)-6-Benzyloxymethyl-12-(tert-butyl-dimethyl-silanyloxy)-2-methoxymethoxy-3-methyl-dodeca-2,8,10-trienoic acid methyl ester 

Relevant academic research and scientific papers

Phosphine-boronates: Efficient bifunctional organocatalysts for Michael addition

Phosphine-boronates R2P(o-C6H4) B(OR′)2 have been evaluated as bifunctional organocatalysts for the Michael addition of malonate pronucleophiles to methylvinylketone. The presence of the Lewis acidic boron center adjacent to phosphorus significantly improves catalytic performance. Isolation and complete characterization of a key intermediate, namely a β-phosphonium enolate, substantiate the role of the Lewis acidic moiety in the catalytic process.