830335-30-3

Upstream product

• 154972-23-3 N-((benzyloxy)carbonyl)-2S-amino-1-phenyl-but-3-ene 
• 1351983-09-9 (E)-1-phenyl-nona-1,8-dien-5-one 
• 1351983-14-6 (E)-1-but-3-enyl-5-phenyl-pent-4-enylamine 
• 39482-39-8 Hex-5-en-2-one N,N-dimethylhydrazone 
• 2687-12-9 cinnamyl chloride 
• 70353-50-3 hept-6-ene-2,5-dione 

Relevant academic research and scientific papers

On the stereoselective bicyclization of aminodienes catalyzed by chelating diamide complexes of the group 3 metals. A direct comparison of Sc(iii) and Y(iii) bis(amide)s with an application to the synthesis of alkaloid 195F

Highly diastereoselective bicyclizations of aminodienes catalyzed by chelating diamide complexes of Sc(iii) and Y(iii) that lead to pyrrolizidines and indolizidines are described. This bis(annulation) procedure has been utilized in a concise synthesis of the pyrrolizidine alkaloid 195F.

Stereoselective synthesis of substituted N-heterocycles via sequential cross metathesis-reductive cyclization

A diastereoselective synthesis of substituted piperidine and pyrrolidine derivatives is presented, employing a highly selective cross metathesis (CM) reaction followed by a domino reduction-cyclization process. A diastereoselective synthesis of substituted mono- and bicyclic-piperidine and pyrrolidine derivatives is presented, employing a highly selective cross metathesis (CM) reaction followed by a domino reduction-cyclization process.