185847-85-2

Upstream product

• 68471-58-9 1-(benzyloxycarbonyl)-1,2,3,4-tetrahydropyridine 
• 762-72-1 allyl-trimethyl-silane 
• 501-53-1 benzyl chloroformate 
• 53708-19-3 4-isopropoxypyridine 
• 66207-23-6 1-benzyloxycarbonyl-1,2,3,6-tetrahydropyridine 
• 185847-84-1 benzyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate 
• 23031-08-5 benzoyl(pyridin-1-ium-1-yl)amide 

Downstream Products

• 185847-87-4 6-(4,4-Dibromo-but-3-enyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 185847-89-6 6-Pent-3-ynyl-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 185847-88-5 6-But-3-ynyl-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 185847-86-3 6-(3-Oxo-propyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 185847-90-9 6-(2-Oxo-ethyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 

Relevant academic research and scientific papers

Direct C-H Allylation of N-Acyl/Sulfonyl Tetrahydroisoquinolines and Analogues

A highly efficient direct C-H allylation reaction at the α position of N-acyl/sulfonyl tetrahydroisoquinolines under mild conditions was developed. The reaction was also suitable for allylation of other protected nitrogen-containing heterocycles. Several

Complexation promoted additions to N-benzoyliminopyridinium ylides. A novel and highly regioselective approach to polysubstituted piperidines

Unprecedented regioselectivities were observed for the addition of different organometallic nucleophiles to N-benzoyliminopyridinium ylides. Even benzylic and branched aliphatic Grignard reagents, which usually give substantial amounts of 1,4-adducts, sho

Exploitation of palladium-catalyzed reductive enyne cyclization in the synthesis of (-)-4a,5-dihydrostreptazolin

Hydroxyl-promoted reductive cyclization of enyne compounds catalyzed by Pd(OAc)2-BBEDA was explored and found to effect constructing the pyrindine framework with the alkylidene appendage. This methodology was applied to the stereoselective synthesis of (-)-4a,5-dihydrostreptazolin.