135910-47-3

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 132553-76-5 [(2R,3S)-2-Chloro-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester 
• 135910-46-2 (1S,2S)-3-Amino-2-chloro-1-(1-trityl-1H-imidazol-4-yl)-propan-1-ol 
• 33016-47-6 (1-tritylimidazol-4-yl)carboxaldehyde 
• 135793-03-2 (R)-3-[(2R,3S)-2-Chloro-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionyl]-4-isopropyl-oxazolidin-2-one 
• 135793-04-3 (2R,3S)-2-Chloro-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionamide 
• 127822-76-8 (+/-)-erythro-β-chloro-γ-hydroxy-1-triphenylmethyl-1H-4-imidazolepropanamine 
• 132553-77-6 [2-Chloro-3-oxo-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester 

Downstream Products

• 132553-77-6 [2-Chloro-3-oxo-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester 
• 110883-46-0 (+/-)-threo-2-amino-β-chloro-γ-hydroxy-1H-4-imidazolepropanamine 
• 132553-74-3 {(2S,3S)-2-Chloro-3-[2-(4-chloro-phenylazo)-1H-imidazol-4-yl]-3-hydroxy-propyl}-carbamic acid tert-butyl ester 
• 127822-76-8 (1S,2S)-3-Amino-2-chloro-1-(1-trityl-1H-imidazol-4-yl)-propan-1-ol 
• 134822-16-5 (5S,6S)-5-Chloro-6-(1-trityl-1H-imidazol-4-yl)-[1,3]oxazinan-2-one 
• 132553-76-5 [(2S,3S)-2-Chloro-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester 
• 127909-96-0 girolline 
• 135910-49-5 {(2S,3S)-2-Chloro-3-[2-(4-chloro-phenylazo)-1H-imidazol-4-yl]-3-hydroxy-propyl}-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Enantioselective Synthesis of Girolline

Girolline (RP 49532) is efficiently and enantioselectively synthesized from the aldol reaction of (R)-3-chloroacetyl-4-isopropyl-1,3-oxazolidin-2-one 2 and 1-triphenylmethylimidazole-4-carboxaldehyde 3 followed by reaction with aqueous ammonia and reducti

A diastereoselective synthesis of girolline

Girolline (RP 49532, 1), a new antitumour agent, was prepared in the racemic series using an oxidation-reduction sequence starting from (±)-erythro-β-chloro-γ-hydroxy- 1-triphenylmethyl-1H-4-imidazolepropanamine 3. The heterocyclic amino function was intr