61865-50-7

Usage

Chemical Properties

Off-White Solid

Upstream product

• 108-24-7 acetic anhydride 
• 77745-28-9 cis-4-Aminocyclopent-2-enemethanol Hydrochloride 
• 61865-62-1 cis-4-aminocyclopent-2-nene-1-carboxylic acid hydrochloride 
• 49805-30-3 2-azabicyclo[2.2.1.]hept-5-en-3-one 
• 77745-25-6 cis-4-amino-2-cyclopentenecarboxylic acid methyl ester hydrochloride 
• 65942-42-9 N-((1R,4S)-4-Hydroxymethyl-cyclopent-2-enyl)-acetamide 

Downstream Products

• 65898-98-8 Acetic acid 3-acetylamino-cyclopentylmethyl ester 
• 72346-00-0 (+/-)-9-<2α,3α-dihydroxy-4α-(hydroxymethyl)cyclopent-1α-yl>adenine 
• 125356-68-5 (+/-)-9-<(1β,3α,4β)-3-fluoro-4-(hydroxymethyl)cyclopentyl>-6-aminopurine 
• 452324-48-0 (+/-)-cis-endo-(4-amino-bicyclo[3.1.0]hex-2-yl)methanol 
• 87419-91-8 (+/-)-(1α,2α,3α,5α)-3-amino-5-(hydroxymethyl)-1,2-cyclopentanediol 
• 72345-98-3 (+/-)-4β-acetamido-2α,3α-dihydroxy-1β-cyclopentanemethanol 
• 122624-75-3 (+/-)-cis-<4-<<2-amino-6-chloro-5-<(4-chlorophenyl)azo>-4-pyrimidinyl>amino>-2-cyclopentenyl>carbinol 
• 122624-79-7 (+/-)-cis-<4-(5-amino-7-chloro-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)-2-cyclopentenyl>carbinol 
• 122624-81-1 (+/-)-cis-5-amino-3,6-dihydro-3-<4-(hydroxymethyl)-2-cyclopentenyl>-7H-1,2,3-triazolo<4,5-d>pyrimidin-7-one 
• 122624-83-3 (+/-)-cis-<4-(5,7-diamino-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)-2-cyclopentenyl>carbinol 
• 118237-88-0 (+/-)-cis-<4-(2,6-diamino-9H-purin-9-yl)-2-cyclopentenyl>carbinol 
• 118353-05-2 (+/-)-cis-2-amino-1,9-dihydro-9-[4-(hydroxymethyl)-2-cyclopenten-1-yl]-6H-purin-6-one 
• 122624-71-9 (+/-)-cis-<3-(5,7-diamino-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)cyclopentyl>carbinol 
• 118237-87-9 cis-(+/-)-2-Amino-6-chloro-9-<4-(hydroxymethyl)-2-cyclopenten-1-yl>-9H-purine 

Relevant academic research and scientific papers

Biocatalytical Transformations- VI. The 4-Acetamido-cyclopent-2-ene Carboxylate Route Revisited: Synthesis of (+)- and (-)-Aristeromycin

Enantiomerically pure (+)-as well as (-)-aristeromycin can be synthesized starting from (+)- or (-)-butyl (or hexyl) 4-acetamido-cyclopent-2-ene carboxylate; these carboxylates are easily obtained from their corresponding racemates by hydrolysis with the lipase from Candida rugosa.

Carbocyclic Sugar Amines: Synthesis and Stereochemistry of Racemic α- and β-Carbocyclic Ribofuranosylamine, Carbocyclic Lyxofuranosylamine, and Related Compounds

The facile and stereoselective synthesis of racemic carbocyclic β-ribofuranosylamine, carbocyclic β-lyxofuranosylamine, and related 2,3-cis-dihydroxy carbocyclic pentofuranosylamines is reported.In addition, the synthesis, isolation, and base-catalyzed epimerization of methyl cis-4-aminocyclopent-2-enecarboxylate are described.The epimerization at C(1) followed by stereoselective cis hydroxylation provides for the first time access to the racemic carbocyclic α-pentofuranosylamines.