90922-50-2

Upstream product

• 7340-23-0 (E)-ethyl 3-(2-pyridyl)-propenoate 
• 7340-23-0 ethyl 3-(pyridin-2-yl)acrylate 
• 694-59-7 pyridine N-oxide 
• 19639-76-0 [D₅]-pyridine-N-oxide 
• 140-88-5 ethyl acrylate 
• 54495-51-1 (E)-3-(2-pyridyl)acrylic acid 

Downstream Products

• 259729-63-0 (2R,3S)-2-Acetoxy-3-benzyloxycarbonylamino-3-(pyridin-2-yl)propionic acid ethyl ester 
• 7340-23-0 (E)-ethyl 3-(2-pyridyl)-propenoate 
• 161024-43-7 (+)-lentiginosine 
• 529474-73-5 (2S,3R)-ethyl 2,3-dihydroxy-3-(N-oxypyridin-2-yl)propanoate 
• 503448-19-9 (2R,3S)-ethyl 2,3-dihydroxy-3-(N-oxypyridin-2-yl)propanoate 

Relevant academic research and scientific papers

Palladium-catalyzed C-H functionalization of pyridine N-oxides: Highly selective alkenylation and direct arylation with unactivated arenes

Two catalytic protocols of the oxidative C-C bond formation have been developed on the basis of the C-H bond activation of pyridine N-oxides. Pd-catalyzed alkenylation of the N-oxides proceeds with excellent regio-, stereo-, and chemoselectivity, and the

Stereoselective synthesis of swainsonines from pyridines

An efficient synthesis of (-)-swainsonine and (-)-2,8a-di-epi-swainsonine was developed starting from readily available 2-pyridinecarbaldehyde and 3-hydroxypyridine. In particular, it was demonstrated that the mixture of simple indolizidines, i.e. lentigi

Asymmetric aminohydroxylation of heteroaromatic acrylates

N-, S- and O-heteroaromatic acrylates were aminohydroxylated with generally high regio- and enantioselectivity. While pyridylacrylates are not amenable towards this process, the corresponding N-oxides proved to be a useful substitute, allowing the access