143539-97-3

Upstream product

• 143539-88-2 C-[(R)-C-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-C-thiazol-2-yl]-methylamine 
• 143539-89-3 1-(tert-Butoxycarbonylamino)-1-deoxy-2,3-O-isopropylidene-1-(2-thiazolyl)-D-erythro-triitol 
• 143539-87-1 N-Benzyl-1-deoxy-1-(hydroxyamino)-2,3-O-isopropylidene-1-(2-thiazolyl)-D-erythro-triitol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 100-39-0 benzyl bromide 

Downstream Products

• 143539-98-4 (4R,5S)-5-Benzyloxymethyl-4-thiazol-2-yl-oxazolidin-2-one 

Relevant academic research and scientific papers

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

Stereocontrolled addition of 2-lithiothiazole to the nitrone derived fromD-glyceraldehyde acetonide. A revision and extension

The sense of diastereoselective addition of 2-lithiothiazole la to the nitrone 2 derived from Dglyceraldehyde is reversed by the use of Lewis acids (Et2AlCl, TiCl4) as complexing agents; the configuration of the hydroxylam