99545-25-2

Upstream product

• 99545-24-1 2-(2,2-dimethoxyethyl)-2-(3,4-dimethoxyphenyl)-1,3-dithiane 
• 50766-67-1 2-(3,4-dimethoxyphenyl)-1,3-dithiane 
• 109-49-9 5-Hexen-2-one 
• 99545-23-0 2-formylmethyl-2-(3,4-dimethoxyphenyl)-1,3-dithiane 

Downstream Products

• 99545-26-3 1-[2-(3,4-Dimethoxy-phenyl)-[1,3]dithian-2-yl]-2-hydroxy-oct-7-en-4-one O-benzyl-oxime 
• 89771-49-3 (±)-lasubine II 
• 99545-20-7 (2R,4R)-2-But-3-enyl-6-(3,4-dimethoxy-phenyl)-2,3,4,5-tetrahydro-pyridin-4-ol 
• 99545-22-9 (2S^*,4S^*,6S^*)-6-(4-hydroxybutyl)-2-(3,4-dimethoxyphenyl)-4-piperidinol 
• 99545-21-8 (2S^*,4S^*,6S^*)-6-(3-butenyl)-2-(3,4-dimethoxyphenyl)-4-piperidinol 
• 99545-28-5 (2R,4R)-4-Amino-1-[2-(3,4-dimethoxy-phenyl)-[1,3]dithian-2-yl]-oct-7-en-2-ol 
• 99545-29-6 {(R)-1-[(R)-4-(3,4-Dimethoxy-phenyl)-2-hydroxy-4-oxo-butyl]-pent-4-enyl}-carbamic acid tert-butyl ester 
• 107977-24-2 ((R)-1-{(R)-3-[2-(3,4-Dimethoxy-phenyl)-[1,3]dithian-2-yl]-2-hydroxy-propyl}-pent-4-enyl)-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Stereoselective Preparation of Acyclic syn-β-Amino Alcohols from β-Hydroxy Ketones via the Corresponding O-Benzyl Oximes

Reduction of β-hydroxy ketone O-benzyl oximes with lithium aluminum hydride in the presence of sodium or potassium methoxide afforded the corresponding syn-β-amino alcohols in highly stereoselective manner.A lythraceae alkaloid, lasubine II, was synthesiz

A NEW APPROACH TO THE SYNTHESIS OF A LYTHRACEAE ALKALOID, LASUBINE II

A lythraceae alkaloid, (+/-)-lasubine II, is synthesized via an acyclic syn-1,3-amino alcohol which is derived stereoselectively from a β-hydroxy ketone.