149180-94-9

Upstream product

• 115822-55-4 (4S,1'S)-4-(1'-benzyloxy-2'-oxoethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 183603-94-3 tert-butyl (4S,1'R)-2,2-dimethyl-4-(1'-hydroxy-4'-pentenyl)oxazolidine-3-carboxylate 
• 183603-95-4 tert-butyl (4S)-2,2-dimethyl-4-(1'-oxo-4'-pentenyl)oxazolidine-3-carboxylate 
• 122709-21-1 (4S)-2,2-Dimethyl-4-(N-methoxy-N-methylcarbamoyl)oxazolidin-3-carbonsaeure-(tert-butyl)ester 
• 336625-45-7 (S)-4-((R)-1-Benzyloxy-4,5-dihydroxy-pentyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 

Downstream Products

• 336625-40-2 tert-butyl (4S,1'R)-4-(1'-benzyloxy-4'-hydroxyhexadecyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 14058-54-9 (-)-deoxoprosophylline 
• 336625-44-6 (2S,3R)-3-benzyloxy-2-benzyloxymethyl-6-dodecyl-2,3,4,5-tetrahydropyridine 
• 336625-41-3 tert-butyl (4S,1'R)-4-(1'-benzyloxy-4'-oxohexadecyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 336625-42-4 (2S,3R)-3-benzyloxy-2-(tert-butoxycarbonylamino)-1-hydroxyoctadecane-6-one 
• 336625-43-5 (2S,3R)-2-(tert-butoxycarbonylamino)-1,3-dibenzyloxyoctadecane-6-one 

Relevant academic research and scientific papers

Stereoselective total synthesis of (-)-deoxoprosophylline

An efficient synthesis of the prosopis alkaloid (-)-deoxoprosophylline has been developed, utilizing the easily available amino acid L-serine as a chiral pool starting material.

Two-carbon chain extension of chiral aldehydes via 2-alkenylthiazoles: Synthesis of γ-functionalized alkanals

The reaction of 2-thiazolylmethylenetriphenylphosphorane (1a) in benzene with various aldehydes gives 2-alkenylthiazoles in variable E/Z ratios. Application of the thiazole-to-formyl deblocking protocol to the mixture of the olefins leads to saturated ald