160343-87-3

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 160343-79-3 (3aS,4S,6aR)-6-{{[(1,1-dimethylethyl)dimethylsilyl]oxy}methyl}-3a,6a-dihydro-2,2-dimethyl-4H-cyclopenta[d]-1,3-dioxol-4-ol 
• 30725-00-9 2,3-O-isopropylidene-D-ribonic-γ-lactone 
• 160343-78-2 (3aR,6aR)-6-{{[(1,1-dimethylethyl)dimethylsilyl]oxy}methyl}-3a,6a-dihydro-2,2-dimethyl-4H-cyclopenta[d]-1,3-dioxol-4-one 
• 160343-77-1 (Z)-5-O-(tert-Butyldimethylsilyl)-4,5-didehydro-2,3-O-isopropylidene-D-erythro-penturono-1,4-lactone 
• 160531-14-6 3,4-O-Isopropylidene-aldehydo-L-ribo-penturono-5,2-lactone 
• 5336-08-3 D-Ribono-1,4-lactone 

Downstream Products

• 160343-88-4 <1S-(1α,4α,5α)>-3-(Hydroxymethyl)-4,5-(isopropylidenedioxy)-1-<(4-methoxybenzyl)oxy>-2-cyclopentene 
• 160343-91-9 <1R-(1α,2α,3α,4α,5α)>-1-<(Benzyloxy)methyl>-2,3-(isopropylidenedioxy)-6-oxabicyclo<3.1.0>hexan-4-ol 
• 160343-93-1 <1R-(1α,2β,3β,4β,5β)>-5-Amino-1-<(benzyloxy)methyl>-2,3-(isopropylidenedioxy)-1,4-cyclopentanediol 
• 160343-90-8 <1R-(1α,2α,3α,4α,5α)>-1-<(Benzyloxy)methyl>-2,3-(isopropylidenedioxy)-4-<(4-methoxybenzyl)oxy>-6-oxabicyclo<3.1.0>hexane 
• 160343-89-5 <1S-(1α,4α,5α)>-3-<(Benzyloxy)methyl>-4,5-(isopropylidenedioxy)-1-<(4-methoxybenzyl)oxy>-2-cyclopentene 
• 160343-92-0 <1R-(1α,2β,3β,4β,5β)>-5-Azido-1-<(benzyloxy)methyl>-2,3-(isopropylidenedioxy)-1,4-cyclopentanediol 
• 160343-94-2 <1R-(1α,2β,3β,4β,5β)>-<1-<(Benzyloxy)methyl>-1,2,3,4-tetrahydroxycyclopentane-5-yl>amino (2,3,4,5-tetra-O-benzyl-1-deoxy-α-D-glucopyranos-1-yl)amino thioketone 
• 160343-95-3 <3aR-(3aα,4α,5β,6β,6aα)>-4-<(Benzyloxy)methyl>-2-<(2,3,4,6-tetra-O-benzyl-1-deoxy-α-D-glucopyranos-1-yl)-amino>-3a,5,6,6a-tetrahydro-4H-cyclopentoxazole-4,5,6-triol 
• 160344-09-2 <3aR-(3aα,4α,5β,6β,6aα)>-4-<(Benzyloxy)methyl>-2-(benzylamino)-3a,5,6,6aα-tetrahydro-4H-cyclopentoxazole-4,5,6-triol 
• 160344-08-1 <1R-(1α,2β,3β,4β,5β)>-<1-<(Benzyloxy)methyl>-1,2,3,4-tetrahydroxycyclopent-5-yl>amino benzylamino thioketone 

Relevant academic research and scientific papers

Synthesis of 6-epi-trehazolin from D-ribonolactone: Evidence for the non-existence of a 5,6-ringfused structural isomer of 6-epi-trehazolin

6-Epi-trehazolin was synthesized in a stereocontrolled manner, and this synthesis provided proof for the non-existence of oxazine structural isomer of 6-epi-trehazolin.

Stereocontrolled syntheses of 6-epi-trehazolin and 6-epi-trehalamine from D-ribonolactone

6-epi-Trehazolin was synthesized in a stereocontrolled manner, and this synthesis proved that an oxazine structural isomer of 6-epi-trehazolin does not exist.