86826-96-2

Upstream product

• 1001919-16-9 benzyl N-allyl-N-(2-hydroxy-3-butenyl)carbamate 
• 79328-85-1 N-benzyloxycarbonyl-1,2-dihydropyridine 
• 120568-74-3 N-allyl-N-(2-hydroxy-3-butenyl)amine 
• 501-53-1 benzyl chloroformate 
• 66643-49-0 ethyl 3-hydroxy-1,2,3,6-tetrahydropiperidine-1-carboxylate 
• 157425-56-4 2,3-Dioxa-5-aza-bicyclo[2.2.2]oct-7-ene-5-carboxylic acid benzyl ester 

Downstream Products

• 174956-47-9 (R)-N-Carbobenzoxy-3-hydroxy-1,2,3,6-tetrahydropyridine 
• 174876-96-1 3-acetoxy-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 1001919-20-5 benzyl 3-[(methoxycarbonyl)oxy]-3,6-dihydropyridine-1(2H)-carboxylate 
• 174956-48-0 benzyl (3R)-3-hydroxy-3,6-dihydropyridine-1(2H)-carboxylate 
• 86827-01-2 benzyl 3-ethyl-3-(2-ethylenedioxyethyl)-1,2,3,6-terahydropyridine-1-carboxylate 
• 86827-05-6 benzyl 3-ethyl-3-methoxycarbonylmethylpiperidine-1-carboxylate 
• 86827-02-3 benzyl 3-ethyl-3-(2-ethylenedioxyethyl)piperidine-1-carboxylate 
• 86827-04-5 3-Carboxymethyl-3-ethyl-piperidine-1-carboxylic acid benzyl ester 
• 86827-03-4 3-Ethyl-3-(2-oxo-ethyl)-piperidine-1-carboxylic acid benzyl ester 
• 82645-04-3 benzyl 3-ethyl-3-methoxycarbonylmethyl-1,2,3,6-tetrahydropyridine-1-carboxylate 
• 82645-03-2 benzyl 3-carboxymethyl-3-ethyl-1,2,3,6-tetrahydropyridine-1-carboxylate 
• 82645-02-1 3-Ethyl-3-(2-oxo-ethyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 86826-97-3 benzyl 3-ethyl-3-hydroxy-1,2,3,6-tetrahydropyridine-1-carboxylate 
• 86827-00-1 benzyl 5-ethyl-3-hydroxy-1,2,3,6-tetrahydropyridine-1-carboxylate 

Relevant academic research and scientific papers

1. 2 - effinity and ring compound derivative as a preparation for treating myeloma drug application

The invention discloses a 1,2-oxa-cyclic compound derivative and a preparation method thereof. A molecular structural general formula of 1,2-oxa-cyclic compound derivative is (I), wherein in the formula, A is (hetero) aromatic ring or non-aromatic ring; R

A new preparation of homochiral N-protected 5-hydroxy-3-piperidenes, promising chiral building blocks, by palladiumCatalyzed deracemization of their alkyl carbonates

The palladium-catalyzed deracemization of N-protected alkyl carbonates of 5-hydroxy-3-piperidenes by use of chiral phosphine ligands is described. A Trost ligand such as (R)-BPA was found to be a suitable chiral ligand for the deracemization, providing N-

SYNTHESIS OF (+/-)-TETRAHYDROPSEUDODISTOMIN, A HYDROGENATION PRODUCT OF ANTINEOPLASTIC ALKALOIDS, PSEUDODISTOMINS A AND B

2-Alkyl-1,2,3,6-tetrahydro-3-pyridinols (6, R2 = H) with trans arrangement of the side chains were prepared by sodium cyanoborohydride reduction of the singlet oxygen adducts (5) of 1,2-dihydropyridine derivatives (4) in the presence of tin(II) chloride.S