143539-91-7

Upstream product

• 622-30-0 N-benzyl hydroxylalmine 
• 13039-93-5 2,2:4,5-di-O-isopropylidene-D-arabinose 

Downstream Products

• 143539-92-8 N-Benzyl-1-deoxy-1-(hydroxyamino)-2,3:4,5-di-O-isopropylidene-1-(2-thiazolyl)-D-manno-pentitol 
• 143539-92-8 N-Benzyl-1-deoxy-1-(hydroxyamino)-2,3:4,5-di-O-isopropylidene-1-(2-thiazolyl)-D-gluco-pentitol 
• 851959-99-4 (3R,4'S,5'R,4''R)-2-benzyl-3-(2',2',2'',2''-tetramethyl-[4',4'']bi[[1,3]dioxolanyl]-5'-yl)-4-methoxy-3,6-dihydro-2H-1,2-oxazine 
• 1053231-46-1 (3R,3aR,6aR)-2-benzyl-3-(1-deoxy-2,3:4,5-di-O-isopropylidene-D-mannito-1-yl)-4,5-oxathiain-4,4-dioxide[3,4-d]isoxazolidine 
• 1053231-47-2 (3S,3aS,6aS)-2-benzyl-3-(1-deoxy-2,3:4,5-di-O-isopropylidene-D-mannito-1-yl)-4,5-oxathiain-4,4-dioxide[3,4-d]isoxazolidine 
• 1233792-22-7 N-benzyl-O-(tert-butyldimethylsilyl)-N-((1S)-2-ethoxy-1-((4S,4'R)-2,2,2',2'-tetramethyl-4,4'-bi(1,3-dioxolan)-5-yl)allyl)hydroxylamine 
• 1104460-74-3 (3S,4'S,4''R,5'R)-2-benzyl-4-(benzyloxy)-3-(2',2',2'',2''-tetramethyl-4',4''-bi-1,3-dioxolan-5'-yl)-3,6-dihydro-2H-1,2-oxazine 
• 7512-17-6 N-Acetyl-D-glucosamine 

Relevant academic research and scientific papers

Regio- and stereoselective synthesis of isoxazolidine derivatives by asymmetric 1,3-dipolar cycloaddition reaction of chiral nitrones with 1-propene-1,3-sultone

(Chemical Equation Presented) Asymmetric 1,3-dipolar cycloadditions of chiral nitrones to 1-propene-1,3-sultone (1) were investigated. Chiral nitrones 6a-e reacted with sultone 1 in toluene at 90°C for 24-36 h to give the corresponding isoxazolidines in m

Stereoselective aminohomologation of chiral α-alkoxy aldehydes via thiazole addition to nitrones. Application to the synthesis of N-acetyl-D-mannosamine

The addition of 2-lithiothiazole to nitrones derived from D-glyceraldehyde and D-arabinose affords anti-adducts from which α-amino aldehydes are revealed by thiazole-to-formyl deblocking. The methodology provides a new synthesis of N-acetyl D-mannosamine