151985-38-5

Upstream product

• 108-55-4 glutaric anhydride, 
• 54247-27-7 1-bromo-6-benzyloxyhexane 
• 100-44-7 benzyl chloride 
• 112-47-0 1,10-Decanediol 
• 95331-19-4 10-(benzyloxy)decane-1-ol 

Downstream Products

• 152141-45-2 (2R,3R)-10-benzyloxy-2,3-epoxydecan-1-ol 
• 151985-41-0 (2S,3S)-10-benzyloxy-2,3-epoxydecan-1-ol 
• 151985-46-5 (3R)-10-benzyloxy-3-(tert-butyldiphenylsilyloxy)decane 
• 151985-49-8 methyl (8R)-8-tert-butyldiphenylsilyloxydecanoate 
• 151985-44-3 (3S)-10-benzyloxy-3-hydroxy-1-p-toluenesulfonyloxydecane 
• 151985-39-6 methyl 10-benzyloxy-2-phenylselenodecanoate 
• 151985-48-7 (8R)-8-tert-butyldiphenylsilyloxydecanal 
• 151985-47-6 (8R)-8-tert-butyldiphenylsilyloxydecanol 
• 151985-40-9 methyl (2E)-10-benzyloxy-2-decen-1-oate 
• 151985-43-2 (3S)-10-benzyloxy-1,3-decanediol 
• 106673-36-3 (2E)-10-benzyloxy-2-decen-1-ol 
• 151985-45-4 (3R)-10-benzyloxy-3-decanol 
• 144482-51-9 methyl 10-benzyloxydecanoate 

Relevant academic research and scientific papers

Synthetic method of acid compound

The invention belongs to the field of organic synthesis, and particularly relates to a synthetic method of an acid compound. An acid anhydride compound and an alkyl bromide or a functionalized alkyl bromide are subjected to a cross-electrophilic coupling reaction to synthesize an acid compound, so that the application of the alkyl bromide in the cross-electrophilic coupling reaction is expanded, and a novel non-traditional method for chemically and selectively constructing a carbon-carbon bond through a decarburization process is provided. The synthesis method is simple, economic, green and environment-friendly, and has wider applicability or is suitable for large-scale production.

4-DIMETHYLAMINOBUTYRIC ACID DERIVATIVES

This invention relates to novel 4-dimethylaminobutyric acid derivatives of the formula wherein A1, A2, R1, m and n are as defined in the description and in the claims, as well as pharmaceutically acceptable salts thereof. These compounds inhibit carnitine palmitoyl transferase (CPT) activity, in particular CPT2 activity, and can be used as medicaments in methods for the treatment of diseases modulated by CPT2 inhibitors.

Lipase inhibiting polymers

The invention features a method for treating obesity in a patient by administering to the patient a polymer that has been substituted with one or more groups that inhibit lipases, which are enzymes responsible for the hydrolysis of fat. The invention furt

Lipase inhibiting polymers

The invention features a method for treating obesity in a patient by administering to the patient a polymer that has been substituted with one or more groups that inhibit lipases, which are enzymes responsible for the hydrolysis of fat. The invention furt

Four New Polyacetylenic Glucosides, Methyl β-D-Glucopyranosyl Helianthenate C-F, from Jerusalem Artichoke (Helianthus tuberosus L.)

Four new polyacetylenic glucosides isolated from the leaf of Jerusalem artichoke (Helianthus tuberosus L.) were characterized as methyl β-D-glucopyranosyl helianthenate C (5), D (6), E (7), and F (8).The absolute stereochemistry of the glucosyloxymethine