124010-25-9

Upstream product

• 171815-24-0 ethyl 4,5-dihydro-4-(phenylmethoxy)-3-isoxazolecarboxylate 
• 171815-20-6 4,5-dihydro-3-nitro-4-(phenylmethoxy)isoxazole 
• 171815-19-3 <<1-(chloromethyl)-2-nitroethoxy>methyl>benzene 
• 171815-21-7 4,5-dihydro-4-(phenylmethoxy)-3-isoxazolecarbonitrile 
• 540-63-6 ethane-1,2-dithiol 
• 171815-22-8 4,5-dihydro-4-(phenylmethoxy)-3-isoxazolecarboxaldehyde 
• 124010-24-8 4,5-dihydro-3-(1,3-dithiolan-2-yl)-4-isoxazole 
• 620-05-3 iodomethylbenzene 

Downstream Products

• 124010-32-8 (4S,5S)-5-Benzyloxy-4-[1,3]dithiolan-2-yl-[1,3]oxazinan-2-one 
• 124010-32-8 (4S,5R)-5-Benzyloxy-4-[1,3]dithiolan-2-yl-[1,3]oxazinan-2-one 
• 124010-26-0 γ-amino-β-(phenylmethoxy)-1,3-dithiolane-2-propanol 
• 124010-26-0 (R*,R*)-γ-amino-β-(phenylmethoxy)-1,3-dithiolane-2-propanol 
• 124010-26-0 (R*,S*)-γ-amino-β-(phenylmethoxy)-1,3-dithiolane-2-propanol 

Relevant academic research and scientific papers

A NEW ROUTE TO 4-OXYGENATED ISOXAZOLINES. APPLICATION TO THE SYNTHESIS OF 2-DEOXY-2-AMINOBUTOSE DERIVATIVES

The THP ether of 4,5-dihydro-3-nitro-4-isoxazol, prepared by a sequential nitroaldol nitrosative cyclization strategy, was converted to a 4,5-dihydro-3-(dithiolanyl)isoxazole; subsequent LBH reduction gave a 95:5 diastereomeric mixture of 2-deoxy-2-aminot

2-Amino-2-deoxytetrose derivatives. Preparation from 4,5-dihydroisoxazoles via reductive cleavage

The 4-alkoxy-3-nitro-4,5-dihydroisoxazoles 2a,b were prepared by condensation of nitromethane and chloroacetaldehyde, protection of the resulting nitroaldol 1c, and subsequent nitrosative cyclization. Multistep replacement of the nitrogroup of 2a,b by a 2