537030-24-3

Upstream product

• 532-20-7 D-arabinofuranose 
• 537030-20-9 (2R,3R,4R)-2,3,5-tris(benzyloxy)-4-hydroxypentanal O-(tertbutyldiphenylsilyl)oxime 
• 537030-18-5 Methanesulfonic acid (1S,2S,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-4-(tetrahydro-pyran-2-yloxyimino)-butyl ester 
• 537030-17-4 (2R,3R,4S)-2,3,5-Tris-benzyloxy-4-hydroxy-pentanal O-(tetrahydro-pyran-2-yl)-oxime 
• 16838-89-4 2,3,5-tri-O-benzyl-L-xylofuranose 
• 100-44-7 benzyl chloride 
• 41546-31-0 L-xylose 
• 160549-10-0 2,3,5-tri-O-benzyl-D-arabinofuranose 
• 2680-03-7 N,N-Dimethylacrylamide 
• 537030-19-6 (2R,3R,4R)-3,4-bis(benzyloxy)-2-((benzyloxy)methyl)-3,4-dihydro-2H-pyrrole 1-oxide 

Downstream Products

• 1620081-28-8 (1R,2R,3R,6R,7aR)-1,2-bis(benzyloxy)-3-[(benzyloxy)methyl]-6-(methylsulfonyloxy)hexahydro-1H-pyrrolizine 
• 1620081-12-0 C₁₆H₂₀N₄O₃ 
• 1620081-09-5 C₆₅H₆₈N₄O₈ 
• 1620081-08-4 C₃₆H₄₄N₄O₅ 
• 1620081-07-3 C₃₃H₃₆N₄O₅ 
• 1620081-06-2 C₃₇H₃₈N₄O₃ 
• 1620081-05-1 C₃₃H₃₈N₄O₄ 
• 1620081-04-0 C₃₇H₄₆N₄O₃ 
• 1620081-02-8 C₂₉H₃₂N₄O₃ 
• 537030-27-6 (1R,2R,3R,6R,7aR)-1,2-bis-benzyloxy-3-benzyloxymethyl-6-metansulfonyloxy-hexahydro-1Hpyrrolizine 
• 537030-26-5 (1S,2R,3R,6R,7aR)-hexahydro-1,2-bis(phenylmethoxy)-3-[(phenylmethoxy)methyl]-1H-pyrrolizine-6-ol 
• 847797-44-8 (1R,2R,3R,7aR)-1,2-bis(benzyloxy)-3-(benzyloxymethyl)-hexahydro-1H-pyrrolizine 
• 537030-25-4 (1R,2R,3R,6R,7aR)-1,2-bis(benzyloxy)-3-[(benzyloxy)methyl]-6-hydroxyhexahydro-5H-pyrrolizin-5-one 

Relevant academic research and scientific papers

Cycloadditions of Sugar-Derived Nitrones Targeting Polyhydroxylated Indolizidines

The 1,3 dipolar cycloaddition reactions of three pentose-derived pyrroline N-oxides with mono- A nd disubstituted alkenes are reported. A strong dependence of the diastereoselectivity of the cycloadditions on the relative configuration of the nitrone ster

6-Azido hyacinthacine A2 gives a straightforward access to the first multivalent pyrrolizidine architectures

The synthesis of the first multivalent pyrrolizidine iminosugars is reported. The key azido intermediates 4 and 31 were prepared after suitable synthetic elaboration of the cycloadduct obtained from 1,3-dipolar cycloaddition of d-arabinose derived nitrone

Synthesis, biological evaluation and docking studies of casuarine analogues: Effects of structural modifications at ring B on inhibitory activity towards glucoamylase

We report the total synthesis of a series of pyrrolizidine analogues of casuarine (1) and their 6-O-α-glucoside derivatives. The synthetic strategy is based on a totally regio- and stereoselective 1,3-dipolar cycloaddition of suitably substitutedalkenes a

Total syntheses of hyacinthacine A2 and 7-deoxycasuarine by cycloaddition to a carbohydrate derived nitrone

Practical syntheses of nitrone 8 by two different approaches from sugars are reported. Its use as a versatile intermediate in highly selective 1,3-dipolar cycloaddition reactions constitutes the key step for novel total syntheses of hyacinthacine A2