666754-29-6

Upstream product

• 666754-26-3 (-)-N-[(R)-2-hydroxy-1-(tert-butyldimethylsilanyloxymethyl)but-3-enyl]benzamide 
• 501-53-1 benzyl chloroformate 
• 666754-28-5 (4R,trans)-4,5-dihydro-4-(tert-butyldimethylsilanyloxymethyl)-2-phenyloxazoline 

Downstream Products

• 666754-30-9 methyl 4(R)-benzoxy-6-(tert-butyldimethylsiloxy)-5(R)-[[N-(phenylmethoxy)carbonyl]amino]hex-2(E)-enoate 
• 1148123-00-5 (2R,3S,4R)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-4,5-dihydroxypentan-3-yl benzoate 
• 1148123-02-7 (2R,3S,4S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-4,5-dihydroxypentan-3-yl benzoate 
• 1148122-95-5 (2R,3S,4R)-4-(benzyloxycarbonylamino)-5-(tert-butyldimethylsilyloxy)-2,3-dihydroxy-pentyl benzoate 
• 1148123-01-6 (2S,3S,4R)-4-(benzyloxycarbonylamino)-5-(tert-butyldimethylsilyloxy)-2,3-dihydroxy-pentyl benzoate 
• 666754-31-0 (2R,3R,4S,6R)-4-benzoxy-6-(tert-butyldimethylsiloxy)-5-[[N-(phenylmethoxy)carbonyl]amino]hexanoic acid methyl ester 2,3,4,6-tetrol 
• 666754-32-1 (3R,4R,5S,6R)-4-benzoxy-6-(tert-butyldimethylsilyloxymethyl)-3,4-dihydroxypiperidin-2-one 

Relevant academic research and scientific papers

Asymmetric synthesis of (-)-swainsonine

(Chemical Equation Presented) We report a new asymmetric synthetic method for (-)-swainsonine utilizing a chiral oxazoline precursor. The key features in this strategy are the diastereoselective oxazoline formation reaction catalyzed by palladium(0), dias

Synthesis of (+)-1-deoxygalactonojirimycin

A total synthesis of (+)-1-deoxygalactonojirimycin has been accomplished using stereoselective dihydroxylation and piperidine formation by catalytic hydrogenation.